benign diseases of ovary
TRANSCRIPT
BENIGN LESIONS OF OVARY
BY
DR.JASMINA BEGUM.
CONTENT- Non neoplastic cyst & benign neoplastic
tumours- Clinical features- Diagnosis- Differential diagnosis- Management- Complications
OVARYTHE HUMAN OVARY HAS A STRICKING PROPENSITY TO DEVELOP A WIDE VARITY OF TUMORS MOST OF WHICH ARE BENIGN.
80% OF ALL OVARIAN TUMORS ARE BENIGN,ALTHOUGH THIS VARIES WITH AGE.
BENIGN LESIONS OF OVARY
NON NEOPLASTIC NEOPLASTIC(BENIGN)
FUNCTIONAL PATHOLOGY
1.Follicular cyst 1.PCOS A. SURFACE EPITHELIUM 2.Corpus luteal cyst 2.endometrioma 1. Serous 3.Theca lutein & 3. T O mass 2. Mucinous granulosa lutein cyst 3. Endometroid 4. Brenner
B.GERM CELL TUMOUR (BENIGN) C. SEX CORD / STROMAL 1. thecoma/fibroma 2. androblastoma
FOLLICULAR CYST (commonest)
CORPUS LUTEUM CYST
THECA LUTEIN CYST
AGE GROUP Adolescent, reproductive age groups ,can occur in perimenopause
Reproductive age Reproductive age
CAUSE Hyperestronism Over activity of corpus luteum
Excess chorionic gonadotropin secreted in GTD, following to ovulation induction drugs
Size
Laterality
Grow ≥3 & ≤8 cm
B/L or U/L
3 – 10 cm
U/L
Large upto 30 cm
B/L
FOLLICULAR CYST CORPUS LUTEUM CYST
THECA LUTEIN CYST
GROSS Thin walled , unilocular , filled with straw coloured fluid
Pink or haemorrhagic cyst, cut section yellowish orange, filled with blood clots
Multicystic, greyish blue colour, filled with straw colour fluid or blood
Histology Lining epithelium Granulosa cells
Luteinised granulosa cell
Theca lutein cells,granulosa lutein cells
C/F Usually asymptomatic , diagnosis incidental
Dull with U/L pelvic pain Rupture with hemoperitoneum more common
Small are asymptomatic, large -discomfort , painRupture/torsion (more common)
Hemorrhagic cyst with unusual appearance simulating a neoplasm
Shows enlarged uterus in the centre and bilateral Theca lutein cysts. The cyst on the left shows a breach in the capsule and the
right cyst with thin hemorrhagic area suggestive of impending rupture
PCOS:-0.5-4%, infertile women, young reproductive age-excess androgen , chronic anovulation-Pathology: ovaries enlarged, stroma increased, capsule thickened, pearly white-c/s: multiple follicles in cortex -Histo: thickened tunica albuginea, stromal hyperthecosis-insulin resistance (acanthosis nigricans)-CF: amenorrhoea, hirsutism, obesity, enlarged PCO.-Investigations Management – Wt. reduction COCP Tt. Of hirsutism Tt. Of infertility
BENIGN OVARIAN TUMORS
Ovarian neoplasm may be divided generally by cell type of origin into three types:
1.epithelial2.stromal3.germ cell
BENIGN OVARIAN NEOPLASMSEPIDEMOLOGY:-Incidence: 1-3% among outpatient , 75% -benign-Racial factors: higher in white population, lowest in japan-Economic status: higher in industrialised countries-Environmental factors:
PATHOLOGY:-Origin: mesoepithelial cells on ovarian surface-Incidence: epithelial tumours—80% of all ovarian tumours serous cystadenoma– 50% of all epithelial tumoursmucinous cysts—12-15%endometroid—10%unspecified—25-27%
Benign ovarian tumors
MUCINOUSCYST ADENOMA
SEROUSCYST ADENOMA
BRENNER BENIGN CYSTIC TERATOMA
INCIDENCE 12-15 % of Epithelial tumors
20-25% of all OV.tumors
50 % of all Epithelial tumors
40% of all ovarian tumors
2 – 3 % of all Epithelial tumors
1 -2% of all ovarian tumors
95 % of Germ cell tumors
15 – 20% of all ovarian tumors
Bilateral
Malignant chance
10%
5 –10%
40%
40%
8 -10%
rare
15 -20%
1 -2%
20- 40 % of all ov. Tumors in pregnancy
TUMOR MUCINOUS SEROUS DERMOID
ORIGINTotipotent surface epithelium of ovary
Totipotent surface epithelium of ovary
germ cells arrested after 1st meoitic division
PATHOLOGYnaked eye : huge size & wt 5-10 kg pedunculated, largest. smooth, lobulated with whitish or bluish white , translucent tumor.
c/s: thick, visid mucin (glycoprotein) colourless multiloculated with papillary. honey combed appearance
naked eye:smooth, shiny, greyish white exuberant papillary projections .
c/s:multilobulated clear fluid (serum) proteins (albumin & globulin)
naked eye: moderate size, capsule tense & smooth
c/s: trabeculated appearance , sebaceous material with hair , clear rokitansky’s protruberance
-microscopy: lined by 1 layer of tall coloumnar epithelium with dark staining basal nuclei without any cilia. Epithelium resemble to those of endocervix.
-complication: rupture pseudomyxoma peritonei & shows adhesions with visera .
microscopy:- lined by cubical epithelium - papillary structures – dense fibrous stroma covered by single or multiple layers of columnar epithelium. ciliated secretory & peg cells. Epithelium resemble to those of endosalpingeal epithelium
micro: stratified squamous epithelium,granulation tissue, may be transitional/ columnar
.
MUCINOUS CYSTADENOMA
SEROUS CYSTADENOMA
SEROUS /MUCINOUS CYSTADENOMA
Gross appearance of a mucinous (A) and serous (B) cystadenoma of the ovary. The mucinous type is generally multiloculated and can be quite large.
BRENNER TUMOUR-U/l , small to moderate, seen after 50 years-Gross: resembles fibroma, smooth solid tumour-C/s: gritty, yellowish grey-Histology: fibrous tissue with transitional epithelium ( walthard cell nests)-Cf: pmb, pseudo meig
ENDOMETROID TUMOUR:-2% of all ovarian tumours-Lined by glandular epithelium-Moderate size, solid, with cystic areas with haemorrhagic fluid.
Gross appearance of a cut-open Brenner tumor.
2. SEX CORD STROMAL OVARIAN NEOPLASMS
Hormone secreting tumors of the ovary.
These tumors include fibromas, Sertoli-Leydig cell tumors (Arrheno–blastomas or androblastomas).
FIBROMA:-origin: stromal cells of ovarian cortex-small sessile nodule, long pedicle ,solid,smooth surfaced tumour-c/s: white -microscopy: interlacing bundles of spindle shaped cells-complication: torsion ,meig syndrome
ANDROBLASTOMA/SERTOLI-LEYDIG CELL TUMOR-testicular adenoma-androgen secreting tumour-seen in women less than 30 year-gynandroblastoma (granulosa + androblastoma cells)-cf: amennorhoea, atrophy of breasts, enlargement of clitoris, body hair growth, deepening of voice.
Gross appearance of an ovarian fibroma.
3. GERM CELL TUMORSTUMORS OF GERM CELL ORIGIN MAY REPLICATE STAGES RESEMBLING THE
EARLY EMBRYO
CAN OCCUR AT ANY AGE
12-15% OF OVARIAN NEOPLASM
60% OF GCTS OCCURS IN CHILDREN
MOST COMMON BENIGN TYPE IS ‘BENIGN CYSTIC TERATOMA’
DERMOID CYST
On clinical examination
Character 1. Age 2. Laterality3. Mobility4. Feel5. Surface6. Ascites7. Growth8. nodules
Malignant• older• Bilateral• Fixed• Solid• Irregular• Present• Rapid• Present
Benign younger unilateral Mobile Cystic Smooth Absent Slow Absent
Criteria on USG
BENIGN• U/L ,uni/multi locular
Cystic areas with regular thin wall thin septa and nonechogenic cavity
• TVS(doppler) shows regular vascular branching
MALIGNANT• B/L, thick wall, thick
septa, echogenic areas in cavity Irregular heterogenous parts
• TVS neovascularisation• Low RI & PI
USG:
• Benign • Malignant
CLINICAL FEATURESAGE:- late child bearing age -dermoid, mucinous adenoma common in reproductive -dermoid common in pregnancysymptoms: -asymptomatic - detected accidently -heaviness in lower abdomen, mass - dull aching pain, - cardiorespiratory & gastrointestinal upset
(nausea, indigestion) -menstrual pattern unaffected except in hormone
producing tumours signs: cachetic , pitting edema legs
ABD EXAMINATION
Inspection -- bulging of lower abdomen mass – central/ one side/ whole abdomen visible veins , flanks – flat Palpation -- cystic / tense cystic freely mobile from side to side with restricted in above down, smooth surface , nontender Percussion -- dull in center resonant in flanks fluid thrill + Auscultation -- friction rub +
Bimanual pelvic examination -- uterus separated from mass groove + between uterus & mass movement of mass p/a fails to move cx lower pole of cyst felt through fornix absence of pulsation of ut vessels thro fornix
D.D
1.Full bladder
2. Pregnancy 3. Pregnancy with fibroid 4. Ascites 5. Fibroid uterus 6. Encysted peritonitis
INVESTIGATION
To confirm diagnosisUSG Tumor markersStraight x-ray abdomenParacentesisLaproscopy
COMPLICATIONS1. Torsion2. Intracystic hge3. Infection4. Rupture5. Malignancy6. Pseudomyxoma peritonei
Torsion: (axial rotation)• 10 – 15%• moderate size & wt• free mobility & long pedicle• common in dermoid or serous cystadenomaCauses:-Trauma, violent physical movement, contraction of preg uterus, intestinal peristalsis.
• Hemodynamic theory• Symptoms- acute pain + lump, vomiting, fever, shock ,
tachycardia. P/A: tense, tender, cystic mass with
restricted mobility P/v: mass abd separate from uterusDD: 1. Disturbed ectopic preg 2. Acute hydramnios 3. Perforating h mole 4. Torsion of subserous pedunculated fibroidRx: Pain– morphine Laparotomy ( cystectomy/ salpingoophorectomy)
INTRACYSTIC HGE: -serous cystadenoma, malignancy.-venous congestion.
INFECTION:-following torsion-organisms – from intestine, uterine tubes.
RUPTURE:-big & tense cyst-trauma, malignancy, papillary type.
PSEUDOMYXOMA PERTONEI:-mucinous ascites-asso with mucinous cyst adenoma ovary, mucocele appendix & gall bladder, intestinal malignancy.-spontaneous perforation -recurrence high, prognosis poor ( infection, intestinal obstr)-Rx: hystrectomy, BSO with removal of mucin, peritoneal implants with appendix.
OVARIAN CYST premenopause women
Cystic teratoma Simple cyst size 5-8 cm
Benign morphologyCA-125 ≤35IU/L
All other cyst
Laproscopic surgery Follow up 3-6 month or COCP
Laproscopy / laparotomy
Increase in sizesymptomatic
Yes No
Laproscopic cystectomy Follow up
Ovarian cyst postmenapause
Simple cyst size 3-5 cm, Benign morphologyCA-125≤ 35IU/L Doppler RI ≥0.4
Size ≥ 5 cmMorphology suspiciousCA-125 ≥35IU/L
Follow up 6 weeks
Increase in sizeCA-125 Rising
Laparotomy
Yes No
Laparotomy Follow up
SURGERY: young women- ovarian cystectomy Oophorectomy (salpingoophorectomy)parous women- TAH+BSOothers- individualisation.laparoscopic cystectomy / ovariotomylaparoscopy/ USG guided aspiration of cyst.
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