radiologic signs for maxillofacial diag

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Radiologic Signs for Maxillofacial Diagnosis

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  • Radiologic Signs for Maxillofacial Diagnosis

  • Dental Signs

  • Dental signsNumber of teethTooth sizeTooth morphologyTooth structureTooth eruption patternTooth positionRegressive changes

  • Large Teeth

  • Large Teeth SINGLEMacrodontiaConnationFusionGeminationSingle central incisor short stature syndromeMULTIPLENormal variantAdjacent to benign vascular, lymphatic or neural tumorLipomatosisUnilateral hyperplasiaPituitary giantism

  • Small Teeth SINGLEMULTIPLE

  • Small Teeth SINGLEMicrodontia (e.g. peg lateral)Supernumerary teethMULTIPLENormal variantDentinogenesis imperfectaTrisomy 21Facial hypoplasiaPituitary dwarfismVascular tumors

  • Single/Few Teeth of Altered Form

  • Single/Few Teeth of Altered Form(Common) Turners tooth (acquired enamel hypoplasia)DilacerationTaurodontismEnamel invaginations (dens in dente)Peg lateral incisorsEnlarged cingulumEnamel evaginations (Leungs premolar)Shovel-shaped incisors

  • Single/Few Teeth of Altered Form(Uncommon)Connation (fusion and gemination)ConcrescenceTwinningTuberculated maxillary lateral/talon cuspHutchinsons teeth and mulberry molars (congenital syphilis)Premolarization of canines and molarization of premolars

  • Single/Few Teeth of Altered Form(Rare)Secondary to mutilating surgerySecondary to radiation therapySecondary to chemotherapy

  • Hypercementosis

  • HypercementosisPhysiologic with passive eruptionIdiopathicPeriodontal diseasePagets disease of boneAcromegalyBenign tumor (cementoblastoma)Apparent in periapical cemental dysplasia

  • Hypodontia/Oligodontia

  • Hypodontia/Oligodontia(common)Previously extracted teethIdiopathicEctodermal dysplasiasPrevious radiation therapyTrisomy 21 (Downs syndrome)

  • Hypodontia/Oligodontia(uncommon)Chondroectodermal dysplasiaFacial hypoplasiaIncontinentia pigmentiiOral-facial-digital (Mhrs) syndromeOculodento-osseous dysplasiaOculomandibulodyscephaly syndrome (Hallerman-Streiff) /continued

  • Hypodontia/Oligodontia(uncommon)Oligodontia and primary mesodermal iris dysgenesis (Riegers syndrome)PHC syndrome (Bks syndrome)Craniofacial dysostosis (Crouzons Sx)Ehlers-Danlos syndromeFocal dermal hypoplasia syndrome (Goltz syndrome) /continued

  • Hypodontia/Oligodontia(uncommon)PyknodysostosisProgeria (Hutchinson-Gilford syndrome)HypoparathyroidismInverted Marfans syndrome

  • Hyperodontia/Supernumeraries

  • Hyperodontia/Supernumeraries (common) IdiopathicCleft palateCompound odontomaCleidocranial dysplasia

  • Hyperodontia/Supernumeraries (uncommon) Osteomatosis intestinal polyposis syndrome (Gardners syndrome)Oculomandibulodyscephaly syndrome (Hallerman-Streiff syndrome)Oral-facial-digital syndromeDistomusAchondroplasiaEhlers-Danlos syndrome

  • Natal teethNormal variantChondro-ectodermal dysplasia (Ellis van Crevald syndrome)

  • Single Failure in Eruption

  • Failure in eruption - single(common)IdiopathicSupernumerary teethHypodontia (non-development of tooth)Mechanical obstruction by other toothRetained primary tooth or tooth rootDentigerous and eruption cysts

    /continued

  • Failure in eruption - single(common)Benign tumor (e.g. odontoma, ameloblastic fibroma, ameloblastic fibro-odontoma, adenomatoid odontogenic tumor)Odontogenic keratocyst Cleft palateAnkylosis and submersionInflammation coronal to erupting toothOverlying tooth with pulpotomy

  • Failure in eruption - single(uncommon) Odontogenic myxomaCherubismUnicystic ameloblastomaLangerhans cell diseaseOssifying fibromaMalignancy and radiation therapyFibrous dysplasiaPost-extraction scar

  • Failure in eruption - multiple

  • Failure in eruption - multiple(common) Fibromatosis gingivaeDrug-induced gingival hyperplasiaCleidocranial dysplasiaCondylar hypoplasia and ankylosisCherubism

  • Failure in eruption - multiple(uncommon)Osteomatosis intestinal polyposis syndrome (Gardners syndrome)Acrocephalysyndactyly (Aperts syndrome)Gingival hyperplasia syndromesChondroectodermal dysplasia Ellis-van Crevald syndrome)Trisomy 21/continued

  • Failure in eruption - multiple(uncommon)Focal dermal hypoplasia (Goltz syndrome)OsteopetrosisRegional odontodysplasiaProgeria ( Hutchinson-Gilford syndrome)PseudohypoparathyroidismPyknodysostosisJuvenile hypothyroidism (cretinism)Ectodermal dysplasias Vitamin D deficiency syndromes

  • Premature Eruption

  • Premature Eruption (common) Normal variantEarly loss of primary teeth

  • Premature Eruption (uncommon) Adjacent benign vascular or neural tumorUnderlying malignant tumorUnderlying osteomyelitisHyperthyroidismPituitary giantismPrevious radiation therapyHypergonadismCushings syndromeAdrenogenital syndrome

  • Early Tooth Loss

  • Early Tooth Loss (common) Rampant dental cariesDentofacial traumaJuvenile periodontosis/periodontitis

  • Early Tooth Loss (uncommon)Langerhans cell diseaseFactitial injuryCyclic neutropeniaMalignancy (leukemia, lymphoma, neuroblastoma, rhabdomyosarcoma)Hyper keratosis palmoplantaris and periodontoclasia in childhood (Papillon- Lefeuvre syndrome)/continued

  • Early Tooth Loss (uncommon)Radicular dentin dysplasiaAcrodynia (pink disease)Other heavy metal poisoningAcatalasiaHyperparathyroidism

  • Early Tooth Loss (rare)Acro-osteolysisSevere RicketsPituitary cachexia syndrome (Simmonds syndrome)Chediak-Higashi syndrome

  • Displaced Teeth/Tooth Buds

  • Displaced Teeth/Tooth Buds (common)Normal variantMalocclusion ImpactionDentigerous cystsOther cystsTraumatic displacementSubmergence

  • Displaced Teeth/Tooth Buds (uncommon)CherubismLateral inflammatory odontogenic cyst of the mandible (Stonemans cyst)Benign giant cell tumorAmeloblastoma and ameloblastic odontomaMelanotic neuro-ectodermal tumor of infancy/continued

  • Displaced Teeth/Tooth Buds (uncommon)Other benign tumorsOsteomyelitis including osteomyelitis of the maxilla in the newbornLangerhans cell diseaseMalignant tumors (e.g. Burkitts lymphoma, lymphosarcoma, neuroblastoma, rhabdomyosarcoma)

  • Coronal Radiolucency in Tooth (common)Dental cariesRadiolucent resin restorationsCervical burnout and Mach phenomenonProximal overlap artifactEnamel hypoplasiaAbrasion, attrition and erosionDens in dente

  • Coronal Radiolucency in Tooth (common)Dental cariesRadiolucent resin restorationsCervical burnout and Mach phenomenonProximal overlap artifactEnamel hypoplasiaAbrasion, attrition and erosionDens in dente

  • Coronal Radiolucency in Tooth (uncommon)Idiopathic internal resorptionExternal resorptionRadiation cariesPulpal diverticulaLeungs premolar (evagination of pulp)Radiolucent internal enameloma

  • Enlarged dental pulp

  • Enlarged dental pulp (common)Rotation of anterior teethDeveloping teethNormal variant (large cornua)TaurodontismInternal resorptionMacrodontia Connation (fusion and gemination)

  • Enlarged dental pulp (uncommon)Enamel evagination (Leungs premolar)Vitamin D resistant RicketsShell teeth of RushtonHypophosphatasiaRenal osteodystrophyPulpal extension into enamel pearl

  • Small dental pulp

  • Small dental pulp (common)Normal variantTeeth in elderly (secondary dentin)Reactive to dentin cariesTraumatically inducedDentinogenesis imperfecta

  • Small dental pulp (uncommon)Osteogenisis imperfectaDentin dysplasias

  • Dental Enamel Aberrations

  • Dental Enamel Aberrations (common)Dental cariesEnvironmental enamel hypoplasia (Turners tooth; neonatal disease; exanthematous fevers; nutritional deficiency; metabolic disease; drug induced; fluorosis)Amelogenesis imperfectas

  • Dental Enamel Aberrations (uncommon)Mucopolysacchaidoses IV (Morquio-Brailsford syndrome)Ehlers-Danlos syndromeHypophosphatasiaHypoparathyroidismRadiation therapy during tooth development

  • Dentin Aberrations (common)Dental cariesIdiopathic internal resorptionDentinogenesis imperfectaRegional odontodysplasia

  • Dentin Aberrations

  • Dentin Aberrations (uncommon)Osteogenesis imperfectaDentin dysplasiasShell teeth of RushtonEhlers-Danlos syndromeRadiation therapy during tooth development

  • Persistent Open Root Apex

  • Persistent Open Root Apex

    Normal variationPost-dentition supernumerary toothNon-vital toothPeriapical pathosis (cyst; granuloma; abscess)Dens evaginatus (Leungs premolar)Idiopathic internal resorption

  • Prematurely Closed Root Apex

  • Prematurely Closed Root Apex

    Previous trauma to toothRadiation therapy during tooth developmentDentinogenesis imperfectaOsteogenesis imperfectaRadicular dentin dysplasia

  • Calcified pulp tissue

  • Calcified pulp tissue

    Pulp stoneNormal variant for elderlyProjection artifact (molars)Reaction to dentin caries or deep restoration Subsequent to traumaCalcareous degenerationSuperimposition of enamel pearlDentin dysplasias Dentinogenesis imperfecta

  • Fractured Tooth AppearanceTrue fractured toothPeriodontal ligament shadow from adjacent toothOverlying lip, cheek or nose lineBone trabecular pattern or nutrient canalAccessory lateral pulp canalAlveolar bone fractureRadiographic artifact (film crimp; static, etc.)

  • External Root Resorption

  • External Root Resorption(normal variants)Physiologic resorption (primary teeth)Traumatic occlusionAberrant resorption of mesial root of lower first molarNormal variant (pulpotomy of primary tooth)Projection artifact (foreshortening)Incomplete formation (tooth development)

  • External Root Resorption(common pathologic)Apical pathosis (cyst; granuloma; abscess)Iatrogenic - excessive orthodontic forceIdiopathic - uncertain causeRe-implantation of avulsed toothRoot canal therapyBenign odontogenic cysts and tumors (especially dentigerous cyst, ameloblastoma and central giant cell granuloma)

  • External Root Resorption(uncommon pathologic)Factitial injuryInostosisMalignant tumors (e.g. lymphoma)OxalosisHyperparathyroidismPeriodontal diseaseForeign body reactionIdiopathic internal resorption

  • Internal Tooth Resorption

  • Internal Tooth Resorption

    IdiopathicTrauma-inducedCaries-inducedCauses of enlarged pulpsPulpal diverticuliExternal resorptionOdontomalacia

  • Dental calculus and look-alikesTrue dental calculusRestoration overhangsBony ledges adjacent teethEnamel pearl

  • Tooth-like Structures (near oral cavity)Avulsed tooth or tooth fragment (trauma or iatrogenic)Supernumerary teethCleft palate associatedCompound odontomaDistomusEpignathus

  • Tooth-like Structures (distant from oral cavity)LithopedionOvarian teratomaOther teratoma (e.g. intra-cranial)

  • Periodontal Signs

  • Radiologic Signs Concerning the PeriodontiumLoss of lamina dura (local)Loss of lamina dura (general)Accentuation of lamina duraWidened periodontal ligament spaceAnkylosisCrestal lucency leading to decreased alveolar bone

  • Localized Loss of Lamina Dura

  • Localized Loss of Lamina Dura(normal variations and confusing shadows)Apex of maxillary canine (canine fossa)Tooth rotationMaxillary premolars before maturationProjection over maxillary sinusTongue out of roof of mouth during panoramicProjection over mandibular canalProjection over mental foramen

  • Localized Loss of Lamina Dura(common pathlogic)Inflammatory periapical pathosis (apical granuloma, cyst or abscess)Simple (traumatic) bone cystPeriapical cemental dysplasiaFocal osteomyelitis

  • Localized Loss of Lamina Dura(uncommon pathlogic)Malignant tumor (e.g. osteogenic sarcoma)Fibrous histiocytomaLangerhans cell disease

  • Generalized Loss of Lamina Dura

  • Generalized Loss of Lamina Dura(common pathlogic)IdiopathicOsteoporosisPagets disease of boneLeukemia

  • Generalized Loss of Lamina Dura(uncommon pathlogic)Metastatic malignancy (especially breast)HyperparathyroidismHypoparathyroidismMultiple myelomaOsteomalaciaRickets (including vitamin D resistant form)Cushings syndrome/continued

  • Generalized Loss of Lamina Dura(uncommon pathlogic)Renal acidosisAcromegalyOxalosisHypervitaminosis DHypovitaminosis CScleroderma (systemic sclerosis)HyperphosphatasiaBurkitts lymphomaThalassemia

  • Accentuation of Lamina Dura

  • Accentuation of Lamina Dura

    Normal variantScleroderma (systemic sclerosis)

  • Widened PDL Space

  • Widened PDL Space(common)Projection effectNormal finding around necks of teethPeriodontal disease (furcation involvement)Periapical inflammationTraumatic occlusionDental trauma (avulsion or fractured root)Jaw fracture through tooth socketRoot shadow cast over sinusScleroderma (systemic sclerosis)

  • Widened PDL Space(uncommon)Re-implantation of avulsed toothDiabetes mellitusPeriodontosisOsteomyelitisMalignant tumors (especially osteogenic sarcoma)Fibrous histiocytomaCystinosisActinomycotic infection

  • Suspision of Tooth Ankylosis

  • Suspision of Tooth Ankylosis True ankylosis of retained primaryTraumaRe-implantationObscuring condensing osteitisInfectionInostosisSocket sclerosis (false ankylosis)Obscuring idiopathic osteosclerosis COMMON UNCOMMON

  • Crestal Radiolucency

  • Crestal Radiolucency(common)Early destructive periodontal diseaseHyperemic decalcificationJuvenile periodontosisFactitial injuryAcute necrotizing ulcerative gingivitis

  • Crestal Radiolucency(uncommon)Langerhans cell diseaseHyperkeratosis palmoplantaris and periodontoclasia in children (Papillon-Lefevre syndrome)LeukemiaLocal malignancy (central or peripheral)Previous radiation therapyHypothuroidism (cretinism/myxedema)/continued

  • Crestal Radiolucency(uncommon)HyperthyroidismHyperparathyroidismPeripheral giant cell granuloma (epulis)Other epulidesCyclic neutropeniaHypophosphatasiaAcrodynia/continued

  • Crestal Radiolucency(uncommon)Acro-osteolysisSelf-mutilative syndromesAcatalasiaPituitary cachexia (Simmonds disease)Chediak-Higashi syndrome

  • Jaw Structure Fine Signs

  • RadiolucencyPeriapical radiolucencyPericoronal radiolucencyRadiolucency lateral to toothSolitary radiolucency (well-defined) not necessarily associated with toothSolitary radiolucency with ragged bordersRadiolucency in maxillary lateral incisor regionNon-cyst-like radiolucency of bone

    /continued

  • RadiolucencyRarefying osteitisBlurring of trabecular patternDiminished number of trabeculaeGeneralized rarefactionMultilocular radiolucencyAmeloblastoma-like radiolunencyRadiolucency below mandibular canalExpansile jaw lesionsLesions\with undulating/crenulated margins/continued

  • RadiolucencyLytic lesions with wide band-like bordersWidened mandibular canalScattered bone destruction separated by normal or near-normal boneShort linear area of radiolucency in inferior cortex of mandibleCyst-like radiolucency with window-like cortical breachingThinned mandibular lower cortex/continued

  • RadiolucencyBallooned mandibular lower cortexAttenuation of shadow of follicle wallDiscontinuity of antral or nasal wallSuspected daughter cystsExternal erosion of boneLesion with no internal structureMultiple separate well-defined lucenciesMultiple osteolytic lesions with punched-out margins

  • Radiopacity and Mixed Radiopacity/RadiolucencyPeriapical mixed lucent/opaquePericoronal mixed lucent/opaquePeriapical homogeneous radiopacitiesSolitary mixed lucent/opaque lesion not necessarily contacting toothMixed lucent/opaque lesion of TMJSclerosing osteitisIncreased girth of individual trabeculae

    /continued

  • Radiopacity and Mixed Radiopacity/RadiolucencyGranular boneSolitary opacity not contacting teethCompound odontomaComplex odontomaOpacity denser than normal boneMultiple separate opacitiesRoot-like density in bonePossible causes of root in bone appearance/continued

  • Radiopacity and Mixed Radiopacity/RadiolucencySuspected foreign body (metallic or non-metallic)Sequestra-like densityTarget lesion (radiopacity with peripheral shadow)Excrescence with bone densityThickened mandibular lower cortexLaminar periosteal new bone/continued

  • Radiopacity and Mixed Radiopacity/RadiolucencyNew periosteal bone with internal lysisSunray spiculation (new bone perpendicular to cortex)Lesions with internal spindly trabeculaeLesions with septae or pseudoseptaeLesions with honeycombed internal structureLesions with wispy internal structure/continued

  • Radiopacity and Mixed Radiopacity/RadiolucencyLesions with internal residual boneLesions with tubular internal structureLesions with internal rounded dense opacitiesLinear striations (driven snow) within jawboneSuspected osteoblastic metastases

  • Radiolucent Lesions

  • Periapical Radiolucency

  • Periapical Radiolucency (normal)Marrow spacePapillae of developing teethMaxillary sinusIncisive foramenNasolacrimal canalsSubmandibular fossaSublingual fossaMandibular canal and mental foramen/continued

  • Periapical Radiolucency (normal)Mental depression (chin)Tomographic plane (including panoramic) artifactProcessing errors ( e.g. developer splash)

  • Periapical Radiolucency (common pathologic)Periapical cyst, granuloma or abscessFibrous healing defectPeriapical cemental dysplasia (early)Periodontal abscess

  • Periapical Radiolucency (uncommon pathologic)Dentigerous cyst of underlying toothTraumatic (simple) bone cystOther cystsOsteomyelitisUnderlying benign tumor (e.g. cementifying/ossifying fibroma)Primary malignant tumor (e.g. leukemia)

    /continued

  • Periapical Radiolucency (uncommon pathologic)Central giant cell granulomaLangerhans cell diseaseLingual salivary gland depression (Stafnes bone cavity)Multiple myelomaMetastatic malignancy (especially breast)/continued

  • Periapical Radiolucency (uncommon pathologic)Early cementoblastoma or osteoblastomaRadicular dentin dysplasiaEarly odontomas

  • Pericoronal Radiolucency

  • Pericoronal Radiolucency (common)Normal dental follicle spaceDentigerous cystEnvelopmental odontogenic keratocystAdenomatoid odontogenic tumorEarly odontoma or ameloblastic fibro-odontoma

  • Pericoronal Radiolucency (uncommon single)Ameloblastic fibromaAmeloblastomaEarly calcifying epithelial odontogenic tumor (Pindborg tumor)Mucopolysaccharidoses (I-H) - Hurlers syndromeEarly calcifying odontogenic cyst

  • Pericoronal Radiolucency (multiple)Dental follicle spacesMultiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Osteomastosis- intestinal polyposis syndrome (Gardners syndrome)MucopolysaccharoidosesRegional odontodysplasia

  • Radiolucency Lateral to Tooth

  • Radiolucency Lateral to Tooth (common)Lateral periodontal abscessLateral periodontal cystEndodontic perforationExtension of disease from adjacent tooth

  • Radiolucency Lateral to Tooth (uncommon)Lateral canal periapical cystOdontogenic keratocystNeurofibroma or neurilemmomaGiant cell granulomaUnilocular ameloblastomaLangerhans cell disease Hyperparathyroidism

  • Well-defined solitary lucency not necessarily contacting teeth (uncommon)Odontogenic keratocystAmeloblastomaGiant cell granulomaEarly ossifying/cementifying fibromaEarly fibrous dysplasiaEosinophilic granuloma

    /continued

  • Well-defined solitary lucency not necessarily contacting teeth (uncommon)NeurofibromaOdontogenic myxomaCentral hemangioma

  • Well-defined solitary lucency not necessarily contacting teeth (rare)Aneurysmal bone cystChondrosarcomaCentral fibromaTuberculous osteomyelitisHydatid cystEarly calcifying epithelial odontogenic tumor (Pindborgs tumor)

  • Single Radiolucency with Ragged Borders

  • Single Radiolucency with Ragged Borders (common)Chronic osteitisOsteomyelitisPeripheral squamous cell carcinomaInfected radicular, residual or other cyst

  • Single Radiolucency with Ragged Borders (uncommon)Early fibrous dysplasiaMetastatic carcinomaMalignant salivary gland tumor involving boneOsteolytic osteosarcomaMultiple myelomaChondrosarcoma/continued

  • Single Radiolucency with Ragged Borders (uncommon)FibrosarcomaLymphosarcomaMelanotic neuroectodermal tumor of infancyLeukemia or Ewings sarcoma Aneurysmal bone cystNeurofibromaOdontogenic myxoma

  • Radiolucency in Region of Maxillary Lateral Incisor

  • Radiolucency in Region of Maxillary Lateral Incisor (common)Incisive fossa/foramenCanine fossaPeriapical cyst, granuloma or abscessRarefying osteitis from adjacent centralOther periapical radiolucencies

  • Radiolucency in Region of Maxillary Lateral Incisor (uncommon)CleftsAberrant foramina in anterior maxillaNasopalatine duct cystOdontogenic keratocystDepression from nasolabial cystPost-surgical defect

  • Non-Cystlike Radiolucency of Bone

  • Non-Cystlike Radiolucency of BoneFocal osteoporotic defectLarge marrow spaceNormal variant of tuberositySparse trabeculation in childMaxillary sinusForaminaSubmandibular fossa/continued

  • Non-Cystlike Radiolucency of BoneSublingual fossaPost-coronoid depressionSigmoid notch shadowAcute osteomyelitisHealing surgical defectDecalcification secondary to overlying inflammation

  • Rarefying Osteitis - Focal Osteomyelitis

  • Rarefying Osteitis - Focal Osteomyelitis (common)Foramina or dental PapillaAntrum or nasal passageMandibular canal or mental foramenLarge marrow spacePeriodontal abscess Apical cyst, granuloma or abscessEarly periosteal cemental dysplasia Healing surgical defect

  • Rarefying Osteitis - Focal Osteomyelitis (uncommon)ActinomycosisPrevious radiation therapyLeukemiaMetastatic malignancy (especially breast)Langerhans cell disease

  • Blurring of Trabecular Pattern

  • Blurring of Trabecular PatternOsteomyelitisDecalcification secondary to inflamed adjacent tissuesRadiodontic pitfall (e.g. motion unsharpness; bend artifact)

  • Diminished Number of Trabeculae

  • Diminished Number of Trabeculae(common)Normal variant in childrenInflammatory diseaseOsteopenic metabolic diseases(uncommon)Anaplastic anemiasPrevious radiation therapyVitamin D deficiency syndromeThalassemia and Sickle cell anemiaNeurofibroma

  • Decreased Size of Trabeculae

  • Decreased Size of Trabeculae(common)Normal variation Infection and inflammationDisuse atrophy of alveolus

    (uncommon)Previous radiation therapyVitamin D deficiency syndromeThalassemia

  • Generalized Rarefaction

  • Generalized Rarefaction (common)OsteoporosisCortisone therapyRheumatoid arthritisProlonged immobilizationMalignant and other cachetic diseases

  • Generalized Rarefaction (uncommon)Cushings syndromeHyperparathyroidismVitamin D deficiency syndromeAcromegalyPancreatitisMalnutritionPregnancy-related changes/continued

  • Generalized Rarefaction (uncommon)Diabetes mellitusScurvyInherited anemiasLeukemiaLangerhans cell diseaseMultiple myelomaPagets disease of boneOsteogenesis imperfectaRenal acidosis

  • Generalized Rarefaction (rare) HypophosphatasiaHyperphosphatasiaHypoparathyroidismThyrotoxicosisHypogonadismAgranulocytosisOxalosisPrevious radiation therapy

  • Multilocular Radiolucency

  • Multilocular Radiolucency(common unilateral)Aberrant normal anatomy (maxillary antrum)AmeloblastomaOdontogenic keratocystCentral giant cell granulomaOdontogenic myxomaMultilocular radicular or residual cyst

  • Multilocular Radiolucency(uncommon unilateral)Mucoepidermoid tumorAneurysmal bone cystArterio-venous malformationCentral hemangiomaAmeloblastic fibromaCalcifying odontogenic cystEarly fibrous dysplasiaDeveloping odontomaLangerhans cell disease

  • Multilocular Radiolucency(rare unilateral)Calcifying epithelial odontogenic tumor (Pindborg tumor)Central fibromaChondromaSporotrichosisCerebroside lipoidosis (Gauchers disease)Oxalosis

  • Multilocular Radiolucency(bilateral)Normal variation for maxillary sinusesCherubismCerebroside lipoidosis (Gauchers disease)Multiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Oxalosis

  • Ameloblastoma-like Radiolucency- Soap Bubble Appearance

  • Ameloblastoma-like Radiolucency- Soap Bubble Appearance (common)AmeloblastomaOdontogenic keratocystGiant cell granulomaMultilocular large radicular or residual cyst

  • Ameloblastoma-like Radiolucency(uncommon)Ameloblastic fibromaTraumatic (simple) bone cystLangerhans cell diseaseOssifying fibromaFibrous dysplasiaCalcifying odontogenic cystSporotrichosisOxalosis

  • Lucency Below Mandibular Canal

  • Lucency Below Mandibular Canal (common)Normal variationSubmandibular fossaLingual salivary gland defect (Stafne)

    (uncommon)Eosinophilic granulomaBenign tumor of salivary gland originSubperiosteal neurofibromaBenign vascular tumor

  • Expansile Jaw Lesions

  • Expansile Jaw Lesions(common)Laminar periosteal new bone ( e.g. osteitis proliferans)AmeloblastomaRadicular or residual cystCentral giant cell granulomaDentigerous cystFibrous dysplasiaCherubism

  • Expansile Jaw Lesions(uncommon)Hemangioma NeurfibromaOsteosarcoma or lymphosarcomaOssifying fibromaAneurysmal bone cyst(rare)Traumatic (simple) bone cystBurkitts lymphoma

  • Lesions with Crenulated (Undulating) Margins

  • Lesions with Crenulated (Undulating) MarginsAmeloblastomaCentral giant cell granulomaOdontogenic myxomaOther benign tumorsOdontogenic keratocystBotyroid lateral periodontal cyst

  • Lytic Lesions with Wide Band-like Borders

  • Lytic Lesions with Wide Band-like BordersInfected cystLateral inflammatory odontogenic cystFibrous dysplasiaGiant cell tumorAneurysmal bone cystOssifying fibroma(common) (uncommon)(rare)OsteoblastomaOsteoid osteoma

  • Widened Mandibular Canal

  • Widened Mandibular CanalNormal variantNeurilemmomaNeurofibromaVascular tumor, hamartoma or malformationMalignant tumor (primary, extension or metastasis)Lymphoma(common) (uncommon)

  • Scattered Bone Destruction Separated by Normal Bone

  • Scattered Bone Destruction Separated by Normal BoneAcute osteomyelitisMultiple myelomaSquamous cell carcinomaActinomycosisOsteoradionecrosisMetastatic carcinomaOxalosisTuberculous osteomyelitis(common) (uncommon)

  • Short Linear Area of Radiolucency in Inferior Cortex

  • Short Linear Area of Radiolucency in Inferior CortexAcute osteomyelitisSquamous cell carcinoma extending into boneOther local malignant destruction (e.g osteogenic sarcoma)

  • Cyst-like Radiolucency with Window-like Cortical Breaching

  • Cyst-like Radiolucency with Window-like Cortical BreachingAmeloblastomaLarge radicular or residual cystOdontogenic myxomaCentral giant cell granulomaNeurofibroma

  • Thinned Lower Cortex (Mandible)

  • Thinned Lower Cortex (Mandible)Multiple myelomaRheumatoid arthritisDiseases associated with generalized rarefactionLangerhans cell diseaseHyperparathyroidismThalassemiaSickle cell anemia(common) (uncommon)(rare)Hemifacial atrophy (Romberg disease) Osteogenesis imperfacta

  • Ballooned Inferior Cortex

  • Ballooned Inferior Cortex(common)Dentigerous cystPeriostitis ossificansLarge radicular or residual cystFibrous dysplasiaCementifying/ossifying fibromaAmeloblastoma Odontogenic myxoma

  • Ballooned Inferior Cortex(uncommon)Central giant cell granulomaNeurofibroma (blister lesion)Hyperparathyroidism (Brown tumor)HemangiomaAmeloblastic fibromaCalcifying odontogenic cyst

  • Ballooned Inferior Cortex(rare)Aneurysmal bone cystBurkitts lymphoma Central fibromaCalcifying epithelial odontogenic tumor (Pindborg tumor)Osteogenic sarcoma

  • Attenuation of Shadow of Follicle Wall

  • Attenuation of Shadow of Follicle Wall (common)Localized infection of primary toothEruption cystAcute osteomyelitis

  • Attenuation of Shadow of Follicle Wall (uncommon)Vitamin D deficiency syndromesLeukemiaLangerhans cell diseaseBurkitts lymphomaLymphosarcomaHyperparathyroidism

  • Attenuation of Shadow of Follicle Wall (rare)Melanotic neuroectodermal tumor of infancyRhabdomyosarcomaNeuroblastoma

  • Discontinuity of Nasal or Antral WallApical inflammationProjection artifactOsteomyelitisOdontogenic myxomaAmeloblastomaInvasive squamous cell carcinomaInvasive salivary gland malignancyLong-standing antritisPrevious surgery(common) (uncommon)(rare)Osteogenic sarcomaLangerhans cell diseaseLymphosarcomaAntral mucocele

  • Suspected Daughter Cysts

  • Suspected Daughter CystsOdontogenic keratocystAmeloblastomaMucoepidermoid tumor (central)Central hemangiomaBotyroid lateral periodontal cyst(common) (uncommon)

  • External Erosion of Bone

  • External Erosion of Bone

    Adjacent squamous cell carcinomaScleroderma (systemic sclerosis) Cystic hygromaSecondary to pulsatile vesselHodgkins diseaseEosinophilic granulomaAdjacent malignant adjacent lymph nodeMetastatic malignancy Secondary to PVC poisoningIdiopathic

  • Lesion with no Internal Structure

  • Lesion with no Internal Structure Odontogenic cystNon-odontogenic cyst Traumatic bone cystAmeloblastomaOdontogenic myxomaHemangiomaNeurofibromaOsteolytic osteogenic sarcomaAmeloblastic fibromaEarly calcifying cyst or tumor(common) (uncommon)

  • Multiple Separate Well Defined Radiolucencies

  • Multiple Separate Well Defined Radiolucencies(common)Normal variationMultiple periapical pathoses (cysts, granulomas or abscesses)Multiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Early stages of periapical cemental dysplasia

  • Multiple Separate Well Defined Radiolucencies(uncommon) (rare)CherubismMultiple myelomaMetastatic carcinomaLangerhans cell disease LymphosarcomaLeukemiaAmeloblastomasSkip lesion of osteosarcomaNiemann-Pick diseaseCerebroside lipoidosis (Gauchers disease)MucopolysaccharoidosesHyperparathyroidism

  • Multiple Osteolytic Lesions with Punched Out Margins

  • Multiple Osteolytic Lesions with Punched Out MarginsMultiple MyelomaLangerhans cell diseaseMetastatic carcinomaHemangiomaBurkitts lymphoma

  • Radiopaque and Mixed Radiolucent/Radiopaque Lesions

  • Periapical Mixed Lucency/Opacity

  • Periapical Mixed Lucency/Opacity Dental cryptRarefying osteitis plus tooth rootMixed rarefying -sclerosing osteitisPeriapical cemental dysplasiaForeign body (e.g. root canal filling material)

    Cementifying/ ossifying fibromaCementoblastomaPagets disease of boneComplex odontomaCompound odontomaCalcifying odontogenic cyst(common) (uncommon)

  • Pericoronal Mixed Lucency/Opacity

  • Pericoronal Mixed Lucency/Opacity Complex odontomaCompound odontomaAdenomatoid odontogenic tumorAmeloblastic fibro-odontomaCalcifying odontogenic cystOdontogenic fibromaCystic odontomaCalcifying epithelial odontogenic tumor (Pindborg tumor)(common) (uncommon)

  • Periapical Radiopacity

  • Periapical Radiopacity(common)Anatomic superimpositionsTori and exostosesRetained roots or unerupted toothRadiographic artifactSclerosing osteitisMature periapical cemental dysplasiaHypercementosisForeign body

  • Periapical Radiopacity(uncommon)Superimposed soft tissue calcificationCementoblastomaOsteoblastomaCementifying/ossifying fibromaMature complex odontomaOsteoblastic metastasesPagets disease of bone

  • Single Mixed Lucency/Opacity Not Necessarily Contacting Tooth

  • Single Mixed Lucency/Opacity Not Necessarily Contacting Tooth(common)Dense bone island/osteosclerosisSclerosing/condensing osteitisOsseous excrescenceFibrous dysplasiaPeriapical cemental dysplasiaHealing surgical defectDeveloping odontomasCementifying/ossifying fibroma

  • Single Mixed Lucency/Opacity Not Necessarily Contacting Tooth(uncommon)Chronic osteomyelitisPagets disease of boneAmeloblastic fibro-odontomaComplex odontomaCompound odontomaCalcifying odontogenic cystSuperimposed soft tissue calcification

  • Single Mixed Lucency/Opacity Not Necessarily Contacting Tooth(rare)OsteoblastomaOsteoid osteomaOsteogenic sarcomaChondrosarcomaOsteoblastic metastases

  • Mixed Lucency/Opacity in Region of Mandibular Condyle Head

  • Mixed Lucency/Opacity in Region of Mandibular Condyle Head

    OsteochondromaChondrometaplasiaOsteomyelitis from middle earHealing traumatic injury to TMJFibrous dysplasiaOssifying fibromaOsteoblastomaOsteogenic sarcoma or ChondrosarcomaCharcots joint

  • Simulating Sclerosing Osteitis

  • Simulating Sclerosing Osteitis(common)Normal variation of trabeculation Superimposed normal structure or toriFocal sclerosing osteomyelitis (condensing osteitis)Florid osseous dysplasia or periapical cemental dysplasia (late stage)Fibrous dysplasiaPagets disease of boneIatrogenic (orthodontic treatrment)

  • Simulating Sclerosing Osteitis(uncommon)Superimposed osteomaSecondary hyperparathyroidismIdiopathic hypercalcemiaSuperimposed submandibular gland stone (sialolithiasis)

  • Simulating Sclerosing Osteitis(rare)OsteopetrosisInfantile cortical hyperostosisOsteoradionecrosisOsteogenic sarcomaOsteoblastic metastasesOsteoblastoma and osteoid osteitisMelorrheostosisMyelosclerosisHealing syphilitic gumma

  • Increased Girth of Individual Trabeculae

  • Increased Girth of Individual Trabeculae Condensing osteitis (focal sclerosing osteomyelitis)Central hemangiomaNeurofibromaFluorosisMyelosclerosisOsteoblastic metastases(common) (uncommon)

  • Granular Bone Fibrous dysplasiaOsteomyelitis (bone replacing sequestrum)Post-surgical defectPagets disease of boneThalassemiaCementifying/ossifying fibromaOsteogenic sarcomaChondrosarcomaHodgkins diseaseRenal osteodystrophy recovery phaseGroundou(common) (uncommon)

  • Granular Bone

  • Solitary Opacity Not Necessarily Contacting Tooth

  • Solitary Opacity Not Necessarily Contacting Tooth(common)Anatomic superimpositionRadiodontic pitfall (fixer splash)Osteosclerosis, exostosis or torusUnerupted tooth or retained rootSclerosing osteitis or socket sclerosisBenign cemental massOdontomaForeign body

  • Solitary Opacity Not Necessarily Contacting Tooth(uncommon)Cementifying/ossifying fibromaCompact osteomaOsteogenic sarcomaChondrosarcomaOsteoblastomaOsteoid osteomaSuperimposed soft tissue calcification

  • Simulating Compound Odontoma

  • Simulating Compound Odontoma Compound odontomaSupernumerary teethComplex odontomaAdenomatoid odontogenic tumorAmeloblastic fibro-odontomaAmeloblastic odontomaDistomusTeratomaEpignathion(common) (uncommon)

  • Simulating Complex Odontoma

  • Simulating Complex Odontoma Complex odontomaPeriapical cemental dysplasia (late phase)Florid osseous dysplasiaCompound odontomaCondensing osteitisCompact osteomaCementifying/ossifyingfibromaOsteogenic sarcomaOsteochondromaAmeloblastic odontomaFibrous dysplasia (late)

    (common) (uncommon)

  • Opacity Denser than Normal Bone

  • Opacity Denser than Normal Bone Foreign body (e.g. fragment of metallic restorative material)OdontomasFlorid osseous dysplasia or periapical cemental dysplasia (late phase)Focal sclerosing osteitisOsteopetrosisFibrous dysplasia PyknodysostosisCompact osteomaOsteogenic sarcomaOsteomastosis-intestinal polyposis syndrome (Gardner Sx)Occulodento-osseous dysplasia

    (common) (uncommon)

  • Multiple Separate Radiopacities

  • Multiple Separate Radiopacities Tori and exostosesPeriapical cemental dysplasiaFlorid osseous dysplasiaMultiple retained roots or impacted teethMultiple socket sclerosisOsteosclerosis including condensing osteitis

    Calcinosis cutisOsteomatosis-intestinal polyposis (Gardner) syndromeEnchondromatosis and hemongiomatosis (Maffuci syndrome)Gigantiform cementomaOverlying soft tissue calcification(common) (uncommon)

  • Root-like Density in Bone

  • Root-like Density in Bone Retained rootDense bone island (osteosclerosis)Coronoid superimpositionRoot displaced in soft tissues/fascial planeSocket sclerosis

    AntrolithBony spicule in antrumPterygoid hamulus superimpositionSuperimposed sialolithOther soft tissue calcificationOsteochondroma

    (common) (uncommon)

  • Causes of Root in BoneSecondary to carious destruction of tooth crownTraumatic injury with tooth fractureIatrogenic (incomplete extraction)Displacement of root into adjacent soft tissues or sinus (superimposition)

  • Suspected Metallic Foreign Body

  • Suspected Metallic Foreign Body Amalgam fragmentBody jewelryOther restoratives or dental instrumentsArtifact (scratched cassettes, fixer splash, panoramic ghosts, etc.)NeedlesShot-gun pelletsLeaded glass fragmentsPaper in cassetteMetal fragment in path of primary beam(common) (uncommon)

  • Suspected Non-Metallic Foreign Body

  • Suspected Non-Metallic Foreign Body Calcified acneCarotid atherosclerosisSialolithiasisCalcified lymph nodeTooth fragmentOsteosclerosisSubclinical fibrous dysplasiaCysticercosisPhlebolithMyositis ossificans(common) (uncommon)

  • Sequestra-like density

  • Sequestra-like density Acute osteomyelitisChronic osteomyelitisOsteoradionecrosisOsteogenic sarcoma

    Also see Single Large Opacities listTuberculosisActinomycosisSyphilisMercury poisoningPhosphorus poisoning (phossy jaw)(common) (uncommon)

  • Target Lesion (Radiopacity with Peripheral Shadow

  • Target Lesion (Radiopacity with Peripheral ShadowRetained primary rootInfection around retained tooth rootSequestraPeriapical cemental dysplasiaOdontomaCementoblastomaCementifying/ossifying fibromaFibrous dysplasia(common) (uncommon)(rare)Brodies abscessOsteoblastomaOsteoid osteoma

  • Excrescence with Density of Bone

  • Excrescence with Density of Bone IdiopathicTori and exostosesOssifying fibrous epulisOsteochondroma

    Soft tissue calcificationsHyperostosisFibrous dysplasiaOsteomatosis-intestinal polyposis syndrome (Gardner/s syndrome)Peripheral chondromaChondrosarcoma(common) (uncommon)

  • Thickened Mandibular Inferior Cortex

  • Thickened Mandibular Inferior CortexSickle cell anemiaSecondary to osteomyelitisFluorosisPhosphorus poisoningMyelosclerosisSclerostosisRarely a variant of normal

  • Laminar Periosteal New Bone

  • Laminar Periosteal New Bone(common)OsteomyelitisPeriostitis ossificans (Garrs osteomyelitis)

  • Laminar Periosteal New Bone(uncommon)Infantile cortical hyperostosisLateral inflammatory odontogenic cyst of the mandible (Stonemans cyst)Superficial surface injuries to faceCervicofacial actinomycosisTuberculosis affecting jaw Syphilitic periostitisEosinophilic granuloma/continued

  • Laminar Periosteal New Bone(uncommon)Hypervitaminosis A or ScurvyLeukemia (single new layer)Osteogenic sarcomaEwings sarcomaNeostosis secondary to hemodialysisIdiopathic periostitis with dysproteinemia (Goldblooms syndrome)Diffuse idiopathic skeletal hyperostoses Sx

  • New Periosteal Bone with InternalDestruction

  • New Periosteal Bone with InternalDestructionChronic osteomyelitisTuberculous osteomyelitisOsteogenic sarcoma

  • New Bone Perpendicular to Original Cortex

  • New Bone Perpendicular to Original Cortex Sickle cell anemiaOsteogenic sarcomaChondrosarcomaOsteoblastic metastasesReticulum cell sarcomaNeuroblastomaThalassemiaSpherocytosisEwings sarcomaBurkitts lymphoaSyphilitic periostitisMeningiomaHemangiomaOssifying fibrous epulisOsteoma

    (common) (uncommon)

  • Lesions with Internal Spindly Trabeculae

  • Lesions with Internal Spindly TrabeculaeOdontogenic myxomaCentral hemangiomaCentral giant cell granuloma (unusual) Ameloblastoma (unusual)

  • Lesions with Septae or Pseudo Septae AmeloblastomaCentral giant cell granulomaOdontogenic myxomaOdontogenic keratocystTraumatic (simple) bone cystCherubismCentral hemangiomaFibrous dysplasiaChondroma(common) (uncommon)

  • Lesions with Honeycombed Internal Structure

  • Lesions with Honeycombed Internal Structure Odontogenic myxomaCentral hemangiomaEwings sarcomaAneurysmal bone cystAmeloblastomaCentral giant cell granulomaNeurofibromaFibrous dysplasiaOsteogenic sarcoma(common) (uncommon)

  • Lesions with Wispy Internal Structure

  • Lesions with Wispy Internal StructureOdontogenic myxomaCentral giant cell granulomaFibrous dysplasiaNeurofibroma

  • Lesions with Internal Residual Bone

  • Lesions with Internal Residual Bone Odontogenic myxomaAmeloblastomaCentral hemangiomaInvasive squamous cell carcinomaFibrous dysplasiaOssifying fibromaOsteochondromaHodgkins diseaseLymphoma(common) (uncommon)

  • Lesions with Tubular Internal Structure

  • Lesions with Tubular Internal Structure Normal vascular channels (nutrient canals)Central hemangiomaArteriovenous malformationSturge-Weber syndrome (tram track calcifications in brain)

    Central giant cell granulomaAmeloblastomaNeurofibroma(common) (uncommon)

  • Lesions with Internal Rounded Dense Radiopacities

  • Lesions with Internal Rounded Dense Radiopacities OdontomasPeriapical cemental dysplasiaFlorid osseous dysplasiaAdenomatoid odontogenic tumorPagets disease of boneFibrous dysplasiaOsteogenic sarcomaChondrosarcomaChondrometaplasia(common) (uncommon)

  • Linear Striations within Jawbone

  • Linear Striations within JawboneNormal variant (infant mandible)Pagets disease of bone (driven snow appearance)Craniometaphyseal dysplasia (Pyles disease)

  • Suspected Osteoblastic MetastasesBreastProstateLiverLungRectum and colonNeuroblastomaOsteogenic sarcomaLeiomyosarcomaHodgkins disease(common) (uncommon)

  • Jaw Structure Gross Changes

  • Gross Structural ChangesPrognathism or retrognathiaMicrognathiaUnilateral small jawEnlargement of part of jawObtuse or aberrant gonial anglePersistent mandibular midline sutureAbsent coronoid(s)Deviation of chinDeformed mandible/continued

  • Gross Structural ChangesIncreased vertical depth of mandibleUnilateral or bilateral absence of condyleCondylar hyperplasiaSuspected jaw fracture(s)Pathologic fractureSuspected hyoid fracturesRadiolucency in condylar neck/headTrue and false TMJ ankylosisIncreased or decreased TMJ space/continued

  • Gross Structural ChangesLimited or increased TMJ movementSmall or enlarged antrumSuspected antral foreign bodyAntral opacification with normal wallsAntral opacification with abnormal wallsAntral opacification with breached corticesAbsent nasal bones Depressed nasal bridgeHypoplasia of maxilla and zygomasClefts

  • Prognathism

  • Prognathism(common)Normal variationRacial variance (Scandinavian and African)Edentulous mandible (apparent)Relative prognathism (e.g. retrognathic midface secondary to cleft)Acromegaly

  • Prognathism(uncommon)Pagets disease of bonePituitary giantismHemifacial hyperplasiaLymphangioma of tongue or cystic hygroma

  • Prognathism(rare)Multiple nevoid multiple basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Craniometaphyseal dysplasia (Pyles disease)Beckwith-Wiedemann syndromeXXXXY syndromeWaardenburg syndrome

  • Retrognathism

  • RetrognathismNormal variantRelative to protrusion of midfaceTMJ ankylosisJuvenile rheumatoid arthritisHemifacial hypoplasiaSubluxation in infancyHypopituitarismProgressive hemiatrophyAgenesis/dysgenesis of mandibleAgnathiaMicrognathia-related (common) (uncommon)

  • Micrognathia

  • MicrognathiaMandibulofacial dysostosis (Treacher-Collins syndrome)Gonadal dysgenesis (Turners syndrome)Juvenile rheumatoid arthritis (Stills Sx)Cleft lip, micrognathia and glossoptosis (Pierre-Robin syndrome)Oculoauricularvertebral dysplasia (Goldenhars Sx) XX and XY Turner phenotype syndrome (Noonans syndrome) Oculomandibulodyscephaly (Hallerman-Streiff Sx)Pyknodysostosis(common) (uncommon)

  • Micrognathia(rare)Bird-headed dwarfismCongenital telangiectatic erythema with growth retardation (Blooms syndrome)5P - (cric du chat) syndromeChondrodysplasia punctata (Conradi-Hnermann syndrome)De Langes syndromeDiastrophic dwarfism/continued

  • Micrognathia(rare)G syndromeCleft palate, flattened facies and multiple congenital dislocations (Larsens Sx)Long arm 21 deletion syndromeMesomelic dwarfismOrofacial digital syndromeOsteodysplasiaProgeria (Hutchinson-Gilford syndrome)/continued

  • Micrognathia(rare)Rubinstein-Taybi syndromeRussell-Silver syndromeShort arm deletion 18 syndromeSmith-Lemli-Opitz syndromeThrombocytopenia-absent radius syndromeTrisomy 13 syndromeTrisomy 18 syndrome

  • Unilateral Small Jaw

  • Unilateral Small JawLateral facial dysplasiaUnilateral TMJ ankylosisForceps delivery traumaRadiation therapy in infancyHemifacial hypoplasiaHemifacial atrophy (Rombergs disease)Partial mandibular agenesisLinear scleroderma(common) (uncommon)(rare)Central hemangiomaNeurofibroma

  • Enlargement of Part of Jaw (anatomically correct)

  • Enlargement of Part of Jaw (anatomically correct)Adjacent hemangiomaAdjacent neurofibromaFibrous dysplasiaHemifacial hyperplasiaPagets disease of bone

  • Obtuse Gonial Angle

  • Obtuse Gonial AngleNormal age changeEdentulous mandibleCondylar hyperplasia - contralateral condyleTrisomy 21Scleroderma (systemic sclerosis)Mucopolysaccharidoses I-H (Hurlers syndrome)Craniometaphyseal dysplasia (Pyles disease)OsteopetrosisHemifacial hypoplasia(common) (uncommon)

  • Aberrant Gonial Angle

  • Aberrant Gonial AngleNormal variantTMJ ankylosisJuvenile rheumatoid arthritisMandibulofacial dysostosis (Treacher-Collins syndrome)SclerodermaNeurofibromaTrisomy 21Marfans syndromeIsolated anomaly(common) (uncommon)

  • Persistent Mandibular Midline Suture

  • Persistent Mandibular Midline SutureNormal
  • Absent or Diminished Coronoids

  • Absent or Diminished CoronoidsPrevious surgeryPanoramic radiograph - outside focal troughLateral facial dysplasiaScleroderma (systemic sclerosis)Radiation therapy in childhood

    Hemifacial atrophy (Rombergs disease)Local or metastatic malignancy related erosionAgnathiaAgenesis(common) (uncommon)

  • Deviation of Chin Towards Affected SideNormal variantMalocclusion (cross-bite)Unilateral TMJ ankylosisCondylar hypoplasiaLateral facial dysplasiaChildhood or forceps fracture of condyleTorticollisHemifacial atrophy (Rombergs disease)Congenital unilateral facial hypoplasiaPartial mandibular agenesis (common) (uncommon)

  • Deviation of Chin Away From Affected SideNormal variantMalocclusion Condylar hyperplasiaSplinting reaction to TMJ painCongenital unilateral hyperplasiaJoint effusion due to traumaHemangioma or neurfibroma induced jaw hyperplasiaTumor in TMJ region (benign or malignant) (common) (uncommon)

  • Deformed Mandibular ShapeCondylar hyperplasiaTrauma with mal-unionCondylar ankylosis (early)Mandibulofacial dysostosis (Treacher-Collins syndrome)Cystic hygromaFlawed panoramic techniqueNeurofibromaHemignathiaCongenital hypo- or hyperplasia of condyleHemifacial atrophy (Rombergs disease)Klippel-Feil anomaladCongenital scapular elevationTorticollisElectrical or thermal burnsRadiation therapy in childhood (common) (uncommon)

  • Increased Vertical Depth of MandibleNormal variantPrognathismAnatomic enlargement of jawPeriostitis ossificansBenign tumor (e.g. ameloblastoma; ossifying fibroma)ThalassemiaOther congenital anemiasSclerosteosisVan Buchems disease (common) (uncommon)

  • Unilateral Failure of Condylar Development

  • Unilateral Failure of Condylar DevelopmentEarly trauma (e.g. forceps delivery)Childhood infections around TMJ (e.g. mastoiditis; otitis media or externa; dental or skin abscess)Lateral facial dysplasiaRadiation therapy in childhoodHemifacial hypoplasiaLinear sclerodermaBenign tumorLocal malignant tumor destruction of growth centerMetastatic malignancy (common) (uncommon)

  • Bilateral Failure of Condylar Development

  • Bilateral Failure of Condylar DevelopmentTraumaMandibulofacial dysostosis (Treacher-Collins Sx)Cleft palate, micrognathia and glossoptosis (Pierre-Robin) syndromeJuvenile rheumatoid arthritis (Stills disease)

    Congenital dwarfismMucopolysacharidosesChildhood radiotherapyProgeria (Hutchinson-Gilford syndrome)Oculomandibulodycephaly (Hallerman-Streiff Sx)Agnathia or micrognathiaCockaynes syndrome

    (common) (uncommon)

  • Condylar Hyperplasia

  • Condylar HyperplasiaHypertrophic arthritisMalignant tumor (e.g. chondrosarcoma)Fibrous dysplasiaPagets disease of bone

    (common) (uncommon)True hyperplasiaBenign tumor (e.g. osteochondroma)Influence of adjacent vascular or neural tumorAcromegaly

    Prognathism

  • Multiple Jaw Fractures

  • Multiple Fractures (common) (uncommon)Severe traumaChild abuseOsteogenesis imperfecta Juvenile idiopathic osteoporosisAchondrogenesisOsteopetrosisPyknodysostosisMucolipidosesMetaphyseal dysplasiaHomocystinuriaIdiopathic

  • Suspected Jaw Fractures (common)True fracturesSuture linesVascular channelsFistulous tractsSymphysis menti (neonate)Osteomyelitis with fragmentationPharyngeal air space shadowVertebral superimpositionsBase of skull superimpositions

  • Suspected Jaw Fractures (uncommon)Previous radiation therapyHyoid bone superimpositionRadiodontic artifactLarge sequestraPathologic fracture

  • Pathologic Fractures

  • Pathologic Fractures (common) (uncommon)Oral squamous cell carcinomaCentral bone malignancy (e.g. multiple myeloma)Metastatic carcinomaOsteoradionecrosis Severe osteomyelitisMarked alveolar atrophyScleroderma (systemic sclerosis)Langerhans cell disease

  • Suspected Hyoid Fracture Normal cartilagenous septaeSuperimposition artifactSevere blunt traumaHanging (often suicide)Homicide (strangulation)

  • Radiolucency in Condylar Head

  • Radiolucency in Condylar HeadElys cyst of degenerative joint diseaseRheumatoid arthritisProjection artifact (e.g. pterygoid pit; air cells extending into zygomatic arch)Bifid condylePrevious traumaVillonodular synovitisCentral giant cell granuloma/continued

  • Radiolucency in Condylar HeadBenign tumor (e.g. myxoma)Primary malignancy (e.g. osteogenic sarcoma; chondrosarcoma; synovial sarcoma; multiple myeloma; adjacent rhabdomyosarcoma; adjacent glandular carcinomas; lymphoma)Metastatic malignancy (e.g. hypernephroma; carcinoma from lower gastrointestinal tract)

  • True TMJ Ankylosis

  • True TMJ Ankylosis (Common)OsteomyelitisTonsillitisOtitis media or externaMastoiditisAdjacent soft tissue infectionDental abscessTuberculosisRheumatoid arthritis (Stills disease)Ankylosing spondylitis(infection) (traumatic)(other)Mandibular fractureForceps delivery

  • True TMJ Ankylosis (Uncommon)Syphilic gummaCancrum oris (noma)TyphoidMasseter cellulitisRheumatic feverMeaslesSecondary to burnCongenital fusion of gums(infection) (traumatic)(other)IatrogenicTemporal muscle fibrosisChronic dislocation of mandible(neoplasia)Invasive malignancyOsteochondroma

  • False TMJ Ankylosis

  • False TMJ Ankylosis (common) (uncommon)Splinting due to TMJ painMalar fracture (fibrous or bony union subsequent to)Coronoid hyperplasiaCoronoid hyperplasia with campylodactylyOsteochondroma

    Scleroderma (systemic sclerosis)Hysterical trismusTemporal muscle fibrosisMyositis ossificans progressivaTorticollisCongenital elevation of scapula

  • Increased TMJ Space

  • Increased TMJ Space (common) (uncommon)Normal variantNon-uniform patient positioningProjection effect (beam angulation)Posturing of jaw by patientDisplaced articular diskEffusion into joint Hemorrhage into jointLoose body in jointAcute suppurative arthritisDisplacement due to fracture of condyle or glenoid fossaMandibular partial agenesisMucopolysaccharidoses

  • Increased Anterior TMJ Space Normal variantBeam angulation or patient position artifactInternal derangement of TMJRetracted position of condyle due to dental occlusionDeep overbiteOverclosure of mandible (especially in edentulous)Rheumatoid arthritisAbsent middle ear

  • Decreased TMJ Space

  • Decreased TMJ Space (common) (uncommon)Excessive vertical angulation of beam during transcranial projectionArthritis (any kind)Gross disk displacement Previous surgical removal of diskBony or other true ankylosis

  • Limited TMJ Movement (common)Normal variantPain reactionInternal derangement of jointTrue or false ankylosis

  • Limited TMJ Movement (uncommon) Scar tissueScleroderma (systemic sclerosis)Fractured zygomatic archCoronoid hyperplasiaMalignancy in joint areaFacial ParalysisTorticollisMyositis osificans progressivaSubmucous fibrosisSecondary to high dose radiation

  • Excessive Translation of TMJ

  • Excessive Translation of TMJ (common) (uncommon)Normal variantLax TMJ capsule Recurrent dislocationsNeurosisEhlers-Danlos syndrome

  • Small Antrum (Normal in Shape)

  • Small Antrum (Normal in Shape) (uncommon)Hemifacial hypoplasia (congenital)Craniometaphyseal dysplasia (Pyles disease)Cleidocranial dysplasiaCraniofacial dysostosis (Crouzons Sx)Other craniostenosesThalassemia and other congenital anemiasHemifacial atrophy (Rombergs disease)Oculomandibulodyscephaly (Hallerman-Streiff syndrome)

  • Suspected Antral Foreign Bodies

  • Suspected Antral Foreign Bodies(common) (uncommon)Tooth root, or restoration fragment (superimposed or real) Panoramic ghost shadowAntrolithBony excrescence/septumOverlying soft tissue calcificationPellets; bullets; shrapnel; auto glass

    Displaced toothBroken dental instrumentDrainage tubesHeavy cosmetics or eyeglass shadowAspergillosis

  • Antral Opacification (Normal Walls)

  • (common) (uncommon)Infectious antritisAllergic antritisMucous retention phenomenonMucositis secondary to dental apical pathosis or periodontitisHemorrhage following trauma

    Antral Opacification (Normal Walls) Antral polypBlocked ostiaAntral polyposisCystic fibrosisMucocele (blocked ostia and antral expansion)Apical dental cyst (rare)Aspergillosis

  • Antral Opacification (Abnormal Walls)

  • (common) (uncommon)Radicular cystOther benign cyst or tumorFibrous dysplasia (thicker)Antral hypoplasia (thicker)Antral malignancy (e.g. carcinoma; lymphoma)

    Antral Opacification (Abnormal Walls) Inverted papillomaOsteomyelitisThalassemiaAgenesis of antrumMucormycosis

  • Antral Opacification (Breached Walls)

  • (common) (uncommon)Oral-antral fistulaDental abscessAntral carcinomaOral squamous cell carcinoma Salivary gland malignancy

    Antral Opacification (Breached Walls) Infectious antritisTrue mucoceleBenign odontogenic tumor (ameloblastoma; myxoma, etc.)Lymphoma or sarcoma

  • Absent Nasal Bones Severe trauma Prior surgeryFacial cleft syndromesArhinencephaly

  • (common) (uncommon)Facial cleft syndromesPrevious surgeryPrevious traumaAchondroplasiaCleidocranial dysplasiaEctodermal dysplasiasCongenital syphilis

    Depressed/Absent Nasal Bones Idiopathic hypercalcemiaCraniometaphyseal dysplasia (Pyles disease)ArhinencephalyAcrodysostosis

  • Hypoplasia of Maxillary and Malar Bones (common) Mandibulofacial dysostosis (Treacher-Collins syndromeAchondroplasiaCraniofacial dysostosis (Crouzons syndrome)Acrocephalysyndactyly (Aperts syndrome)

  • Hypoplasia of Maxillary and Malar Bones (uncommon) Bird-headed dwarfismCongenital telangiectatic erythema with growth retardation (Blooms syndrome)Cochaynes syndromeDe Lange syndromeOculoauriculovertebral dysplasia (Goldenhars syndromeLeprechaunism (Donohues syndrome)Long arm 18 deletion syndromeLong arm 21 deletion syndrome /continued

  • Hypoplasia of Maxillary and Malar Bones (uncommon) Marshall syndromeMietens-Weber syndromeOculodento-osseous dysplasiaOculomandibulodyscephaly (Hallerman-Streiff syndrome)Oral-facial-digital syndromeOropalatal digital syndromeProgeria (Hutchinson-Gilford syndrome) /continued

  • Hypoplasia of Maxillary and Malar Bones (uncommon) PyknodysostosisRubenstein-Taybi syndromeRussel-Silver syndromeTrisomy 13Trisomy 18Weill-Marchesani syndrome

  • Enlarged Maxilla

  • (common) (uncommon)Normal variantRelative to mandible (see retrognathia)Influence of adjacent or contiguous vascular tumorPagets disease of boneFibrous dysplasiaOsteopetrosis

    Enlarged Maxilla Juvenile hypothyroidism (cretinism)ThalassemiaInfluence of adjacent or contiguous neural tumorCraniopharyngioma

  • (common) (uncommon)Cleft lip and palate Isolated cleft palate (unilateral vs bilateral; anterior vs posterior; complete vs incomplete)

    Cleft Palate ArhinencephalyCleft palate, micrognathia and glossoptosis (Pierre-Robin syndrome)Miscellaneous other craniofacial syndromes

  • Soft Tissue SignsCopyright of Allan G. Farman

  • Radiologic Signs Concerning Facial Soft TissuesCalcifications of facial soft tissuesCalcifications in muscle and subcutaneous tissuesWidespread soft tissue calcificationSolitary large calcified mass adjacent boneLymph node calcificationsCalcifications in submandibular gland region/continued

  • Radiologic Signs Concerning Facial Soft TissuesCalcification in parotid duct regionSialolithiasisAir in soft tissueNasopharyngeal massMacroglossiaSalivary gland enlargementDuctal stricture on sialography/continued

  • Radiologic Signs Concerning Facial Soft TissuesIncreased retropharyngeal space (child)Increased retropharyngeal space (adult)Soft tissue mass with underlying bone involvementSuspected soft tissue tumor shadow

  • Calcification in Facial Soft Tissues

  • (common) (uncommon)

    Calcified acneCalcified lymph node (often post tuberculosis)PhlebolithsCalcified hematomaCalcified adipose tisssueNon-calcification (e.g. tooth displaced into soft tissues)

    Calcification in Facial Soft Tissues Myositis ossificans (traumatic)Myositis ossificans progressivaEhlers-Danlos syndromeScleroderma (systemic sclerosis)Calcinosis universalisCysticercosisHypervitaminosid D

  • Calcifications in Muscles and Subcutaneous Tissues

  • Calcifications in Muscles and Subcutaneous Tissues (common)Dermatolysis and calcinosisGoutScleroderma (systemic sclerosis)Vascular calcificationsRheumatoid arthritisHealing abscess

  • Calcifications in Muscles and Subcutaneous Tissues (uncommon) HyperparathyroidismHypoparathyroidismMultiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Ehlers-Danlos syndromeIdiopathic hypercalcuriaMyositis ossificans (traumatic and progressiva) /continued

  • Calcifications in Muscles and Subcutaneous Tissues (uncommon) ParaplegiaCalcified parasites (e.g. cysticercosis)Carbon monoxide poisoningFracture segmentTumoral calcinosisSecondary to thermal burn or frostbiteBenign or malignant soft tissue tumorLupus erythrematosus

  • Widespread Calcification in Soft Tissues

  • (uncommon)Calcinosis universalisHypoparathyroidismScleroderma (systemic sclerosis)Multiple vascular calcifications

    Widespread Calcification in Soft TissuesGoutHyperparathyroidismImmobilizationLupus erythematosusCysticercosisTumoral calcinosisIdiopathic hypercalcemiaGross metabolic bone breakdown/metastatic calcification (common)

  • Vascular Calcification

  • (uncommon)Carotid atherosclerosisHemangiomaRanine varicesPhlebolithsFamilial arteriosclerosis Vascular Calcification Monkbergs sclerosisEnchondromatosis-hemangiomata Sx (Maffucis syndrome)AneurysmProgeria (Hutchinson-Gilford syndrome)LipodystrophyRenal transplantationWerners syndromeGeneralized calcification of infancy (common)Secondary arteriosclerosis (e.g. diabetes; Cushings Sx; nephrotic Sx)(rare)

  • Solitary Large Calcified Mass Adjacent to Bone

  • (uncommon)Sialolithiasis in Whartons duct (superimposition) Calcified fatCalcified hematoma Solitary Large Calcified Mass Adjacent to BoneScleroderma (systemic sclerosis)OsteochondromaGoutHyperparathyroidismSoft tissue osteo- or chondrosarcomaTumoral calcinosisMyositis ossificansForeign body (common)

  • Calcification in Lymph Nodes of Face

  • (uncommon)Tuberculosis (active or scar)SarcoidosisIdiopathic Calcification in Lymph Nodes of Face HistoplasmosisBCG vaccinationCoccidiomycosisFiliarisLymphomaOsteoblastic metastases (common)

  • Calcification in Submandibular Area

  • (uncommon)Sialolithiasis (in duct or gland)Root or tooth displaced in soft tissuesCalcified lymph nodeForeign bodyCalcification in Submandibular Area Chondrodystrophica calcificans congenitaMyossitis ossificans (common)PhlebolithCalcinosis universalisSclerodermaRadiographic artifact(rare)

  • Calcification in Parotid Area

  • (uncommon)Sialolithiasis (in duct or gland)ArtifactPhlebolithForeign bodyCalcification in Parotid Area (common)Calcinosis universalisMyossitis ossificansOther soft tissue calcifications including metastatic calcification related to metabolic disease

  • Sialolith Appearance

  • (uncommon)True sialolithFilm artifactSuperimposition of tooth in soft tissue or in boneSuperimposed tori, exostoses or osteosclerosisCalcified lymph nodeForeign body

    Sialolith AppearanceGoutHyperparathyroidismImmobilizationLupus erythematosusCysticercosisTumoral calcinosisIdiopathic hypercalcemiaGross metabolic bone breakdown/metastatic calcification (common)

  • (uncommon)Gas producing odontogenic infectionSurgical emphysema from air rotor or during endodonticsProjection of air in sulci in occlusal view Air/Gas in Soft TissueCraters of ulcerative malignancyCrushing injury to thoraxPersistent severe coughingLipomatous accumulation projected over muscle(common)

  • Nasopharyngeal Mass (common)Adenoids/tonsillar tissue (especially in adolescence)InfectionsProjection of posterior aspect of inferior turbinates

  • Nasopharyngeal Mass (uncommon) HematomaMalignant nasopharyngeal neoplasm (carcinoma; lymphoma; lymphoepithelioma; multiple myeloma; chordoma)Benign nasopharyngeal neoplasm (juvenile angiofibroma; neurilemmoma, angioma)Dermoid cyst /continued

  • Nasopharyngeal Mass (uncommon) Extension of neoplasm from sphenoid sinusExtension of neoplasm from nasal passageAntral-choanal polyp (rare)Sarcoidosis or tuberculosisMeningioma extending from base of skullEncephalocoele

  • Macroglossia (common)Normal variant or spread following loss of teethTrisomy 21 (Downs syndrome)AcromegalyHamartoma (lymphangioma or hemangioma)NeurofibromaEdema following trauma or allergic reactionPrimary or secondary amyloidosisLingual thyroid

  • Macroglossia (uncommon)Juvenile hypothyroidism (cretinism)Glycogen storage diseaseAngioneurotic edemaInfant of diabetic motherMucopolysaccharoidosesMuscular dystrophyHappy-puppet syndromeBeckwith-Wiedemann syndrome

  • Salivary Gland Enlargement (common)Paramyxovirus parotitis (mumps)SialolithiasisIdiopathicSjgrens syndromeSuppurative sialadenitisPleomorphic adenoma

  • Salivary Gland Enlargement (uncommon)Chronic alcoholismHormonal imbalanceMalnutrition (e.g. protein deficiency)Mikuliczs syndromeHashimotos diseaseTuberculosis or sarcoidosisBenign or malignant tumorsOncocytosisMucoviscoidoses

  • (uncommon)InflammationSialolithiasis Stricture of Salivary DuctNormal variantCarcinomaTrauma including factitial injury and surgeryRadiation therapy(common)

  • (uncommon)Enlarged adenoids and tonsilsArtifactRetropharyngeal extension of upper respiratory tract disease or odontogenic infection Increased Retropharyngeal Space (childhood)Juvenile nasopharyngeal angiofibromaSevere chest traumaCretinismCystic hygroma or hemangiomaForeign body impactionRetropharyngeal goiterSpinal lesion(common)

  • (uncommon)Infections extending from upper respiratory tractInfections extending from odontogenic causes Increased Retropharyngeal Space (adulthood)ChordomaCarcinomaRetropharyngeal goiterZenkers diverticulumRheumatoid arthritis of spine(common)

  • Soft Tissue Mass with Underlying Bone Erosion

  • Soft Tissue Mass with Underlying Bone Erosion Oral squamous cell carcinomaKaposis sarcoma (often in AIDS)Nasolabial cystPyogenic granuloma including pregnancy epulisOther gingival epulides and denture-induced gingival hyperplasiaNeurofibromatosis (blister region)Salivary gland malignancyMetastatic malignancy (in extraction site)(common)

  • Soft Tissue Mass with Underlying Bone Erosion Lymphoma in soft tissuesMalignant lymph nodeAmyloidosisAngiomaFungal diseasesHemophiliaSarcoma in soft tissues(uncommon)

  • Suspected Soft Tissue Tumor Shadow in Facial Region Primary soft tissue tumors casting their own radiographic shadows are all uncommon in the oral cavity

    Key to relative frequency in next 5 charts: * = relatively common; ** = uncommon; *** = rare

  • Suspected Soft Tissue Tumor Shadow in Facial Region (Muscle) Rhabdomyosarcoma**Leiomyoma***Leiomyosarcoma***(Fat)Lipoma*Liposarcoma***

  • Suspected Soft Tissue Tumor Shadow in Facial Region

    Fibromatosis*Fibrosarcoma**Fibrous histiocytoma **Other aggressive fibrous lesions**(Connective tissue)

  • Suspected Soft Tissue Tumor Shadow in Facial Region

    Neurofibroma *Neurilemmoma**Neurosarcoma***Neuroblastoma**(Neural tissue)(Vascular)

    Hemangioma* Hemangiopericytoma**Angiosarcoma***Kaposis sarcoma*

  • Suspected Soft Tissue Tumor Shadow in Facial Region Oral squamous cell carcinoma*Salivary gland tumors*Metastatic malignancy** (male = lung; prostate; kidney; colon; rectum; liver/female = breast; lung; thyroid; kidney; colon; rectum) (Epithelial)

  • Suspected Soft Tissue Tumor Shadow in Facial Region

    Acute (e.g. cellulitis)*Chronic (e.g. fibro-epithelial polyp)*Condylomata/warts*Other epulides*(Inflammatory)Hematoma*Aneurysms***Mesenchymoma***Soft tissue sarcoma***Accessory muscle mass*** Dermatologic lesions*

    (Miscellaneous)

  • Part 6: Skull SignsCopyright of Allan G. Farman

  • Radiologic Signs Concerning the SkullCraniostenosesMicrocephaly and macrocephalyFrontal bossingBasilar invaginationHypoplasia of skull baseLocalized increase in calvarial densityGeneralized increase in calvarial density/continued

  • Radiologic Signs Concerning the SkullLocalized increased density of skull baseGeneralized increased density of skull baseLocalized thinning of calvariaGeneralized thinning of calvariaGranular bone in skullErosion of inner diploeButton sequestra/continued

  • Radiologic Signs Concerning the SkullSolitary calvarial radiolucencyRadiolucent skull defect in childhoodMultiple calvarial radiolucenciesEnlargement or destruction of sellaSmall sella and J-shaped sellaMultiple wormian bonesPresence of fontanelle shadows/continued

  • Radiologic Signs Concerning the SkullDefective cranial ossificationHair-on-end calvarial densitySolitary intracranial opacityMultiple intracranial opacitiesBasal ganglia calcificationHypertelorismHypotelorism/continued

  • Radiologic Signs Concerning the SkullBrachycephalyDolichocephalyTrigonocephalyTurricephaly and acrocephalyCopper-beaten appearance

  • CraniostenosisCraniofacial dysostosis (Crouzons disease)Acrocephalosyndactyly (Aperts syndrome)Acrocephalopolysyndactyly (Carpenters Sx)Chotzens syndromePfeiffers syndromeCraniometaphyseal dysplasia (Pyles disease) /continued

  • CraniostenosisDiaphyseal dysplasia (Engelmanns Sx)Idiopathic microcephalyIdiopathic hypercalcemiaHypophosphatasiaHyperthyroidismHypervitaminosis D /continued

  • CraniostenosisMandibulofacial dysostosis (Treacher-Collins syndrome)MucopolysaccharidosesRubenstein-Taybi syndromeVan Buchems diseaseTrisomy 21 (Downs syndrome)Head binding/papoose board

  • Microcephaly (Small Skull)

  • Microcephaly (Small Skull)Craniosynostosis syndromesArhinencephalyCockaynes syndromeCri du chat syndromeDe Lange syndromeDysautonomia (Riley-Day syndrome)Focal dermal hypoplasia (Goltz syndrome) /continued

  • Microcephaly (Small Skull)Hypospadias-dysphagia (G syndrome)HomocystinuriaIdiopathic small brain and anencephalyIncontinentia pigmentii (Bloch-Sulzberger syndrome)Myotonic dystrophy (Steinerts syndrome)Nanocephalic dwarfism (Seckels syndrome) /continued

  • Microcephaly (Small Skull)Pancytopenia-dysmelia (Fanconis Sx)PhenylketonuriaPrenatal and neonatal irradiation or infection (e.g. toxoplasmosis)Smith-Lemli-Opitz syndromeTrisomy 13, trisomy 18 or trisomy 21Tuberous sclerosis (Bourneville-Pringle Sx)Normal variant

  • Macrocephaly (Large Skull)

  • Macrocephaly (Large Skull)Hydrocephalus (including Dandy-Walker Sx)Achondroplasia or achondrogenesisCleidocranial dysplasiaCongenital anemiasCraniometaphyseal dysplasia (Pyles disease)Diaphyseal dysplasia (Engelmanns disease)Cerebral giantism (Sotos syndrome) /continued

  • Macrocephaly (Large Skull)Familial macroencephalyIntracranial tumor or subdural hematoma in childhoodBeckwith-Wiedmann syndromeMucopolysaccharidosesPituitary dwarfismRussel-Silver syndrome Apparent with certain craniostenoses

  • Frontal Bossing

  • Frontal BossingEctodermal dysplasiasMultiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)AchondroplasiaCleidocranial dysplasiaOculomandibulodyscephaly (Hallerman-Streiff syndrome) /continued

  • Frontal BossingOsteopetrosisRubenstein-Taybi syndromeOtopalatodigital syndromeOral-facial-digital syndromeHemolytic anemiasHealed ricketsMucopolysaccharidosesCongenital syphilis

  • Basilar invagination

  • Basilar invaginationAchondroplasiaAnkylosing spondylitisCleidocranial dysplasiaKlippel-Feil anomaladOsteogenesis imperfectaOsteomalaciaPagets disease of bone

    /continued

  • Basilar invaginationLangerhans cell diseaseMucopolysaccharidosesOsteopetrosisOsteoporosisPyknodysostosisRheumatoid arthritisSyphilis or tuberculosisTrauma-induced

  • Hypoplasia of Skull Base

  • Hypoplasia of Skull BaseAchodroplasiaChondroectodermal dysplasia

  • Localized Increase in Calvarial Density

  • Localized Increase in Calvarial DensityFibrous dysplasiaHyperostosis frontalis internaCalcifying epithelioma of MalherbeDense bone island as normal variantOsteoblastic metastasisSuperimposed soft tissue calcification (scalp or brain)Late sequel after electrical burn

  • Generalized Increase in CalvarialDensity

  • Generalized Increase in CalvarialDensityAcromegalyAnemias (sickle cell anemia; thalassemia; congenital spherocytosis; elliptocytosis)Childhood cerebral atrophyCongenital cyanotic heart diseaseChronic increased intracranial pressureCranial hemiatrophy /continued

  • Generalized Increase in CalvarialDensityCraniometaphyseal dysplasia (Pyles disease)Craniostenoses (all causes)Diaphyseal dysplasia (Engelmanns disease)Dilantin medicationMyotonic dystrophy (Steinerts syndrome)Fibrous dysplasiaHyperostosis frontalis interna /continued

  • Generalized Increase in CalvarialDensityHyperparathyroidismHyperphosphatasiaHypervitaminosis DHypo/ pseudohypoparathyroidism IdiopathicIdiopathic hypercalcemiaMelorrheostosis /continued

  • Generalized Increase in CalvarialDensityMeningiomaMicrocephalyMucopolysaccharoidosesMyelosclerosisOsteoblastic metastasesOsteogenesis imperfectaOsteopetrosis /continued

  • Generalized Increase in CalvarialDensityOtopalataldigital syndromePagets disease of boneSclerosteosisSecondary polycythemiaSyphilitic osteitisTreated hydrocephalusTreated rickets /continued

  • Generalized Increase in CalvarialDensityTuberous sclerosis (Bourneville-Pringle syndrome)Van Buchems disease

  • Generalized Increase Opacification of Skull Base

  • Generalized Increase Opacification of Skull BaseCraniometaphyseal dysplasia (Pyles disease)Diaphyseal dysplasia (Engelmanns disease)Fibrous dysplasiaFluorosisHealed vitamin D resistant ricketsHyperparathyroidism (following treatment)Hypervitaminosis D /continued

  • Generalized Increase Opacification of Skull BaseIdiopathic hypercalcemiaJuvenile hypothyroidism (cretinism)MelorrheostosisMeningiomaNeurofibromatosisOsteodysplasiaPagets disease of boneSevere anemia

  • Localized Increase Opacification of Skull Base

  • Localized Increase Opacification of Skull BaseAcromegalyChondrosarcomaChordoma with calcificationChronic periostitisFibrous dysplasiaLymphomaMastoiditis

    MeningiomaNasopharyngeal carcinomaOsteoblastic metastasesOsteochondromaOsteogenic sarcomaSclerosteitisSphenoid sinusitis

  • Generalized Thinning of Calvarium

  • Generalized Thinning of CalvariumNormal variant (parietal thinning)Chronic subdural hematomaCongenital arachnoid cystLeptomeningeal cystLocalized temporal lobe hydrocephalusNeurofibromatosisPorencephalic cystSlow-growing intracranial tumor

  • Localized Thinning of Calvarium

  • Localized Thinning of CalvariumCleidocranial dysplasiaCraniolacunaHydrocephalusHypophosphatasiaOsteogenesis imperfectaProgeria (Hutchinson-Gilford Sx)Vitamin D deficiency syndromes

  • Granular Bone in Skull

  • Granular Bone in SkullElectrical burnHereditary anemiaHyperparathyroidism (primary or secondary)IdiopathicLeukemiaLong term steroidsMetastatic carcinoma or neuroblastoma Multiple myelomaOsteomalaciaOsteomyelitisOsteoporosisPagets diseaseMeningiomaOsteoradionecrosisSyphilis

  • Erosion of Inner Diploe

  • Erosion of Inner DiploeArteriovenous malformationChronic subdural hematomaCisterna magna anomalyEosinophilic granulomaEpidermoid cystGliomaHemangioma of skullMeningioma MetastasisNeoplasm of duraPacchionian granulationPorencephalySinus pericranii

  • So-called Button Sequestra

  • So-called Button SequestraEosinophilic granulomaHemangiomaMetastatic carcinomaOsteomyelitisSurgical defectRadiation necrosisSyphilisTuberculosis

  • Solitary Radiolucency in Calvarium

  • Solitary Radiolucency in CalvariumArachnoid cystArteriovenous malformationBenign tumor of scalpCarcinoma of scalpCholesteatomaDermal sinusFibrous dysplasia

    /continued

  • Solitary Radiolucency in CalvariumFractureHemangiomaHyperparathyroidismIdiopathicLymphomaLangerhans cell diseaseMeningoceleMetastasis

    Multiple myeloma NeurofibromatosisNormal variant (venous lake)Osteogenic sarcomaOsteomyelitisPost-surgical defectSarcoidosis, syphilis or tuberculosis

  • Radiolucent Defect in Skull of Child

  • Radiolucent Defect in Skull of ChildArteriovenous malformationCentral or peripheral hemangiomaEpidermoid cystFibrous dysplasiaHemophilic pseudotumorLangerhans cell diseaseNeurofibromatosis (blister lesion) /continued

  • Radiolucent Defect in Skull of ChildNormal fontanelleNormal variant (venous lake)OsteomyelitisMetastatic neuroblastomaOsteogenic sarcomaSurgical defect

  • Multiple Calvarial Radiolucent Defects

  • Multiple Calvarial Radiolucent DefectsCerebroside lipoidosis (Gauchers disease)CraniolacunaHyperparathyroidismLangerhans cell diseaseLeukemia or lymphomaLipid reticuloendothelioses (Niemann-Pick disease) /continued

  • Multiple Calvarial Radiolucent DefectsMetastatic malignancyMultiple myelomaOsteoradionecrosisOsteomyelitisPacchionian granulationsNormal variant (parietal foramina)Sarcoidosis, syphilis or tuberculosisSurgical defects

  • Enlarged or Eroded Sellae

  • Enlarged or Eroded SellaeBenign tumor of base of skullChordomaCraniopharyngiomaEmpty sella syndromeEnlargement of internal carotid arteryHyperparathyroidismHypogonadismIncreased intracranial pressure /continued

  • Enlarged or Eroded SellaeJuvenile hypothyroidism (cretinism)Juxtasellar or suprasellar tumorsMucopolysaccharoidoses I-H (Hurlers syndrome)Metastatic malignancyNasopharyngeal or sphenoid sinus neoplasmOptic sheath tumorOsteomyelitis /continued

  • Enlarged or Eroded SellaePituitary tumorRathkes cleft cystTumor of frontal lobe of brain

  • Small Sella

  • Small SellaCushings syndromeMyotonic dystrophy (Steinerts syndrome)Genetic dwarfismHypopituitarismJuvenile hypothyroidism (cretinism)Normal variant /continued

  • Small SellaPost-partum pituitary necrosis (Sheehans syndrome)Prader-Willi syndromeRadiation therapy in childhoodTrisomy 21

  • J-Shaped Sella

  • J-Shaped SellaHydrocephalusJuvenile hypothyroidism (cretinism)Mucopolysaccharoidosis I-H (Hurlers syndrome)NeurofibromaNormal variantPituitary tumorSuprasellar tumor

  • Multiple Calvarial Wormian Bones

  • Multiple Calvarial Wormian BonesCleidocranial dysplasiaHypophosphatasiaJuvenile hypothyroidism (cretinism)Normal variantOsteogenesis imperfectaOculomandibuldyscephaly (Hallermann-Streiff syndrome) /continued

  • Multiple Calvarial Wormian BonesOtopalatodigital syndromePachydermoperiostitisPrader-Willi syndromeProgeria (Hutchinson-Gilford syndrome)PyknodysostosisTrisomy 21Vitamin D deficiency syndromes

  • Presence of Fontanelle Shadows

  • Presence of Fontanelle ShadowsNormal in early infancyCerebrohepatorenal syndromeCleidocranial dysplasiaCutis laxaDysplasia epiphysealis punctata (Conradis disease)Frontonasal dysplasiasHypophosphatasia

    /continues

  • Presence of Fontanelle ShadowsIntracranial tumorsJuvenile hypothyroidism (cretinism)Oculomandibulodyscephaly (Hallermann-Streiff syndrome)OsteodysplasiaOsteogenesis imperfectaOtopalatodigital syndromePachydermoperiostitis

    /continues

  • Presence of Fontanelle ShadowsPediatric rubella infectionProgeria (Hutchinson-Gilford syndrome)PyknodysostosisRubenstein-Taybi syndromeRussel-Silver syndromeTrigonocephaly causesTrisomy 13, trisomy 18 or trisomy 21

  • Defective Cranial Ossification

  • Defective Cranial OssificationCleidocranial dysplasiaHydrocephalusJuvenile hypothyroidism (cretinism)Langerhans cell disease (Letterer-Siewe variety)NeurofibromatosisOsteogenesis imperfectaPachydermoperiostitis

    /continued

  • Defective Cranial OssificationPrematurityProgeria (Hutchinson-Gilford Sx)PyknodysostosisRenal osteodystrophyVitamin D deficiency syndromes

  • Hair on End Calvarium

  • Hair on End CalvariumHereditary anemias (thalassemia; sickle cell anemia; spherocytosis; elliptocytosis)Congenital heart diseaseEwings sarcomaHemangiomaIron deficiency anemiaMeningioma

    /continued

  • Hair on End CalvariumMetastatic neuroblastomaMetastatic thyroid carcinomaMultiple myelomaOsteogenic sarcoma ChondrosarcomaPolycythemia vera

  • Solitary Intracranial Opacity

  • Solitary Intracranial OpacityArachnoid granulationArteiovenous malformationAtherosclerosisCalcified choroid plexusCalcified cerebral infarctCalcified diaphragma sellaCalcified dura (falx; tentorium; sagittal sinus)

    /continued

  • Solitary Intracranial OpacityCalcified hematomaCalcified petroclonoid or interclinoid ligamentChondrosarcoma of skull baseCraniopharyngiomaCysticercosisEncephalofacial angiomatosis (Strurge-Weber syndrome) /continues

  • Solitary Intracranial OpacityEpendyomaEpidermoid or dermoid cystForeign body (e.g. artery clip)Healed granuloma or abscessHemangioma (sclerosing)IdiopathicMeningiomaMetastatic neoplasm /continued

  • Solitary Intracranial OpacityOsteochondromaOsteoradionecrosisPineal gland Pituitary adenomaRubellaSyphilitic gummaTuberous sclerosis (Bourneville-Pringle Sx)

  • Multiple Intracranial Opacities

  • Multiple Intracranial OpacitiesAneurysmAtherosclerosisBasal ganglia calcificationsIdiopathicEncephalofacial angiomatosis (Sturge-Weber syndrome)Healed brain abscessesCarbon monoxide intoxication

    /continued

  • Multiple Intracranial OpacitiesCockaynes syndromeCytomegalo virus inclusion diseaseEncephalitisHematomasHepatolenticular degeneration (Wilsons disease)HyperparathyroidismHypervitaminosis D

    /continued

  • Multiple Intracranial OpacitiesLipoid proteinosisMetastatic malignancyMultiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Multiple tumors (e.g. meningiomas)NeurofibromatosisParasitic diseaseToxoplasmosisTuberous sclerois

  • Basal Ganglia Calcifications

  • Basal Ganglia CalcificationsBirth anoxiaCarbon monoxide poisoningCockaynes syndromeEncephalitisHemorrhageHypoparathyroidismIdiopathicLead intoxicationParkinsonism /continued

  • Basal Ganglia CalcificationsPrevious radiation therapyPseudohyperparathyroidismToxoplasmosisTuberous sclerosis

  • Hypertelorism(increasedinterorbitalwidth)

  • HypertelorismAcrocephalysyndactyly (Aperts Sx)Anterior meningocoeleCentral facial hypoplasiaCerebral giantism (Sotos syndrome)Cleidocranial dysplasiaCraniostenosis causesCri du chat syndromeDe Langes syndromeDysplasia epiphysealis punctata (Conradis syndrome)

    /continued

  • HypertelorismFacial duplicationFibrous dysplasiaHypertelorism-hypospadias syndromeIdiopathicLarsens syndromeMetaphyseal chondrodysplasiaMetaphyseal dysplasiaMidline dermoid or teratomaMulopolysaccharidoses I-H (Hurlers Sx)

    /continued

  • HypertelorismMultiple nevoid basal cell carcinoma syndrome (Gorlin and Goltz syndrome)Noonans syndromeOrofacial digital syndromeOsteogenesis imperfectaOtopalatodigital syndromeThalassemiaMandibulofacial dysplasia (Treacher-Collins syndrome)Turners syndrome

  • Hypotelorism(decreasedinterorbitalwidth)

  • HypotelorismArhinencephalyGlycogen storage diseaseOculodento-osseous dysplasiaPhenylketinuriaTrigonocephaly Trisomy 13Trisomy 21

  • Unilateral Exophthalmos

  • Unilateral ExophthalmosCraniostenosis causesDermoid cystEpidermoidFibrous dysplasiaFracture with retro-orbital blood or airHemangiomaHyperthyroidismLacrimal gland tumorMeningioma

    /continued

  • Unilateral ExophthalmosMetastatic diseaseMucoceleMucormycosisNeurofibromatosisOrbital meningocoeleBenign tumor (e.g. ossifying fibroma)Osteoma of paranasal sinusOsteomyelitisPagets disease of bone

    /continued

  • Unilateral ExophthalmosPrimary orbital soft tissue diseasePseudotumor of orbitRetro-orbital abscess or cellulitisSinusitis

  • Destructive Lesions with Exophthalmos

  • Destructive Lesions with ExophthalmosChloromaLangerhanss cell diseaseLymphomaMetastatic neuroblastomaMetastatic carcinomaPrimary carcinomaBurkitts lymphoma

  • Enlargement of Superior Orbital Fissure

  • Enlargement of Superior Orbital FissureAneurysm of internal carotid arteryChordomaCraniopharyngiomaExtension of orbital malignancyLangerhans cell diseaseMeningiomaMetastatic carcinoma to sphenoid boneMiddle cranial fossa mass /continued

  • Enlargement of Superior Orbital FissureNeurofibromaNeurofibromatosisNormal variantPituitary tumorPosterior orbital encephalocele

  • Prominent Muscle Attachment

  • Prominent Muscle AttachmentAcromegalyNormal variantAnkylosisPseudo-ankylosisMasseteric hypertrophy

    **