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Cutaneous Malignancy (Nonmelanoma Skin Cancer) Shashidhar S. Reddy, MD, MPH Advisor: Shawn D. Newlands, MD, PhD The University of Texas Medical Branch, Department of Otolaryngology, Grand Rounds Presentation January 21, 2004

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Page 1: Cutaneous Malignancy (Nonmelanoma Skin Cancer) · Management - Cryosurgery ... Cutaneous Malignancy (Nonmelanoma Skin Cancer) Shashidhar S. Reddy, MD, MPH Advisor: Shawn D. Newlands,

Cutaneous Malignancy (Nonmelanoma Skin Cancer)

Shashidhar S. Reddy, MD, MPH

Advisor: Shawn D. Newlands, MD, PhD

The University of Texas Medical Branch,

Department of Otolaryngology,

Grand Rounds Presentation

January 21, 2004

Page 2: Cutaneous Malignancy (Nonmelanoma Skin Cancer) · Management - Cryosurgery ... Cutaneous Malignancy (Nonmelanoma Skin Cancer) Shashidhar S. Reddy, MD, MPH Advisor: Shawn D. Newlands,

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Overview

Incidence and Epidemiology

Normal Skin Histology

Basal Cell Carcinoma

Squamous Cell Carcinoma

Treatment of Cutaneous Malignancy

Rare Cutaneous Malignancies

Conclusions

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Incidence and Epidemiology

800,000 cases per

year

Incidence is

increasing

Mortality is

decreasing

Most occur in

patients over 60

years

80%

15%

4%1%

Basal Cell

Squamous Cell

Melanoma

Etc.

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Incidence and Epidemiology - Etiology

Ultraviolet light – Sun Exposure

– Ionizing radiation causes mutation of tumor suppressor genes

– UV B light: 280-320nm, UV A light 320-400nm

– Amount of UV B radiation is inversely proportional to ozone

– Amount of UV B exposure during childhood and adolescence is directly proportional to risk for BCCA

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Etiology – Sun Exposure

The following groups have the least melanin

and are at greatest risk for BCCA:

– fair complexion,

– light hair,

– blue/green eyes,

– inability to tan,

– history of multiple or severe sunburns,

– Celtic ancestry

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Etiology – Other Factors

Arsenic

Radiation Therapy

Burns, Scars, Ulcers

Immunosuppression

Albinism

Bazex's syndrome (basal cell carcinomas, follicular atrophoderma, hypotrichosis, and hypohidrosis or hyperhidrosis)

Gorlin's syndrome (multiple basal cell carcinomas, pitting of the palms and the soles of the feet, mandibular cysts, spine and rib anomalies, calcification of the falx cerebri, and cataracts )

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Normal Skin Histology

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Normal Skin Histology

Stratum Corneum

Stratum Lucidum

Stratum

Granulosum

Stratum Spinosum

Stratum Basale

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Basal Cell Carcinoma

Slowly growing

malignancy of the

epidermis

Rarely metastasizes

(.028-.55%)

Cells appear

histologically similar to

basal cells of epidermis

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Basal Cell Carcinoma

Clinical subtypes

– Nodular

– Superficial

– Pigmented

– Morpheaform

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Basal Cell Carcinoma

Nodular

– Discrete, raised, circular

– Central ulceration

– Pink, waxy rolled borders

– Relatively non-

aggressive

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Basal Cell Carcinoma

Superficial

– Threadlike, waxy border

– Red, scaling patches

– Spread by radial

extension

– Uncommon in Head and

Neck

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Basal Cell Carcinoma

Pigmented

– Resemble nevus or

melanoma

– Behave the same as

nodular variant

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Basal Cell Carcinoma

Morpheaform

– Macular, whitish, or

yellowish plaque

– Indistinct clinical margins

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Basal Cell Carcinoma

Histology

– Large oval nuclei with

little cytoplasm

– Nuclei are uniform

– Connective tissue

stroma causes

palisading

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Basal Cell Carcinoma

Histologic Subtypes

– Solid

– Cystic

– Adenoid

– Keratotic (Basosquamous)

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Basal Cell Carcinoma

Solid – no cellular

differentiation

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Basal Cell Carcinoma

Cystic

– Differentiation towards

sebaceous glands

– Cystic spaces within

tumor lobules

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Basal Cell Carcinoma

Adenoid

– Glandular pattern

– Lacelike pattern

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Basal Cell Carcinoma

Keratotic (Basosquamous)

– Basal cell CA with

differentiation towards hair

structures

– Shows feature of both basal

cell and squamous cell

carcinomas

– More aggressive clinically

– Undifferentiated cells in

combination with

parakeratotic cells and horn

cysts

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Squamous Cell Carcinoma

More aggressive in terms of local invasion

and rate of metastasis than BCCA (2-5%)

Often a progression from sun-damaged

areas

– Actinic Keratoses

– Bowen’s disease

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Squamous Cell Carcinoma

Actinic Keratosis

– Indicator of severe sun-

damage

– <1cm diameter, scaly

– Face, scalp, hands,

forearms

– Progression to SCCA in

20%

– Cryotherapy, Shave

Excision, 5-FU, TCA

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Squamous Cell Carcinoma

Bowen’s disease

– Carcinoma in situ

– Well-circumscribed,

erythematous scaly patch

with irregular border

– Common in people with

chronic arsenic ingestion

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Squamous Cell Carcinoma

Clinically, SCCA

presents as a crusting,

erythematous,

ulcerated lesion with a

granular friable base.

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Squamous Cell Carcinoma

Histology

– Irregular masses of epidermal cells proliferating

into dermis

– Keratinization in well-differentiated tumors

– Range in degree of anaplasia

– Subtypes of Verrucous, Adenoid squamous, and

Spindle Pleomorphic

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Squamous Cell Carcinoma

Histopathology

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Squamous Cell Carcinoma

Verrucous

– Minimal atypia

– Individual cell

keratinization

– White, cauliflower

lesions

– Uncommon in Head and

Neck

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Squamous Cell Carcinoma

Spindle-Pleomorphic

– Anaplastic

– Little keratinization

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Squamous Cell Carcinoma

Adenoid Squamous

– Anaplasia

– Acantholysis

– Tubular and adenoid

appearance

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Squamous Cell Carcinoma

Histologic Grading of Cutaneous Squamous Cell Carcinoma Googe, Paul B., DermPath Update Volume 1 Number 4 - December 31, 1995

Broders UTMCK Microscopic Appearance

Grade 1 Well differentiated, moderately well

differentiated

abundant keratinization, little nuclear

anaplasia < 25% undifferentiated

cells

Grade 2 Moderately differentiated 50% keratinizing, nuclear anaplasia

present < 50% undifferentiated

cells

Grade 3 Moderately to poorly differentiated less than 25% keratinizing, nuclear

anaplasia extensive < 75%

undifferentiated cells

Grade 4 Poorly differentiated extensive nuclear anaplasia, little or

no keratinization

includes spindle cell and

undifferentiated carcinomas >

75% undifferentiated cells

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Squamous Cell Carcinoma

Table 2: Indicators of Metastatic Potential

Size > 2cm Poorly differentiated (Broders 3 or

4)

Thickness > 2mm Perineural invasion

Invasion of reticular dermis or

subcutaneous tissue

Immunosuppression

Invasion of muscle, bone, or

cartilage

Marjolin’s Ulcer

Anatomic site:

Ear, lip

Locally recurrent

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Management

Initial evaluation involves

– Assessment of location

– Punch or excisional biopsy

– Staging

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Management - Staging

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Management - Curettage

Curettes used to remove tumor by feel with

small margin of normal tissue

After several cycles, wound is treated

topically

Reserved for histologically and clinically

favorable basal cell carcinomas.

Not used for squamous cell lesions

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Management - Cryosurgery

Cryogen such as liquid Nitrogen to kill tumor

cells

Typical temperature of -50°C .

Tissue-sparing, but leave open wound

Hypopigmentation and scarring may result

Limited to favorable small lesions with well-

defined borders

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Management – Radiation Therapy

Used extensively in the past, now sparingly

High cure rate (95%)

Does not allow surgical staging

Protracted treatment course, and expensive

Radiodermatitis, delayed carcinogenesis

Currently reserved for poor operative

candidates, adjuvant in high risk malignancy

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Photodynamic Therapy

Photosensitizing drug (porphyrin, 5-ALA) applied topically, orally or parenterally and localizes into tumor cells

Drug is activated by exposure to light (laser)

Efficacy is low (45%)

Side effects include local edema, erythema, blistering, ulceration

Used as palliation

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Management - Excisional Surgery

Most often used by surgeons, esp for larger lesions

Can be with cold steel or laser

Can allow reconstruction in the same sitting

Frozen sections decrease recurrence rate

Can be time consuming and inconvenient

If more than 1/3 of a cosmetic facial unit is excised, better cosmesis with removal of entire unit

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Management – Excisional Surgery

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Mohs Surgery - Indications

Recurrent skin cancer

Skin cancer in “high risk anatomic areas” and cosmetically important areas

Histologically aggressive skin cancer

Large skin cancers

Skin cancer with ill-defined clinical margins

Irradiated skin

Dermatofibrosarcoma Protuberans

Selected mucosal squamous cell cancers

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Lymphatic Dissection

No hard and fast rules governing lymphatic dissection in N0 Necks

Elective Parotidectomy for deeply invasive tumors of the periauricular region

Large SCCA (>2cm), recurrent SCCA, Marjolin’s ulcer, perineural invasion may require regional lymphadenectomy

Sentinel Lymph Node Dissection may be useful

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Lymphatic Dissection

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Merkel’s Cell Carcinoma

Tumor of presumed mechanoreceptor origin

arising in dermis

Poorly differentiated histology

High rate of recurrence and lymph node

metastasis requires excisional surgery with

adjuvant radiation and treatment of lymphatic

drainage in most cases

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Merkel’s Cell Carcinoma

solitary erythematous to

deep purple plaque or

nodule of up to several

centimeters in size

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Merkel’s Cell Carcinoma

Histology - small, round, basophilic cells

arranged in sheets, rests, or trabeculae

Stains for cytokeratins 8, 18, 20

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Other Rare Cutaneous Malignancies

Dermatofibrosarcoma Protuberans – Arises in dermis, spreads deeply

– Large indurated plaque with firm irregular flesh colored nodules

– Mohs is treatment of choice

Pilomatrix Carcinoma – Arises from Pilomatricoma, a benign tumor of hair

matrix origin

– Aggressive wide local excision is treatment

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Conclusions

Incidence and Epidemiology

Normal Skin Histology

Basal Cell Carcinoma

Squamous Cell Carcinoma

Treatment of Cutaneous Malignancy

Rare Cutaneous Malignancies

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Bibliography

25. Lo JS, Snow SN, Reizner GT, Mohs FE, Larson PO, Hruza GJ. Metastatic basal cell carcinoma: report of twelve cases with a review of the literature. J Am Acad Dermatol 1991;24: 715-9.

Sassmannshausen, MD et al “Pilmatrix carcinoma: A report of a case arising from a previously excised pilomatrixoma and a review of the literature,” J Am Acad Dermatol 2001;44:358-61.

Geh JL et al “Unusual multiple pilomatrixomata: case report and review of the literature,” British Journal of Plastic Surgery. 1999; 52(4):320-1

Chih-Shan Jason Chen, “Dermatofibrosarcoma Protuberans,” emedicine.com, October 30, 2003.

Swanson, NA, “Mohs surgery: technique, indications, applications, and the future.” Arch Dermatol 1983; 1, 19:761.

Boone, John L, “Merkel Cell Tumors of the Head and Neck,” emedicine.com, September 8, 2003

Stucker, Fred J. “Cutaneous Malignancy,” Bailey, Byron J. Head & Neck Surgery – Otolaryngology, Lippincott Williams and Wilkins, Philadelphia, 2001.

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Cutaneous Malignancy (Nonmelanoma Skin Cancer)

Shashidhar S. Reddy, MD, MPH

Advisor: Shawn D. Newlands, MD, PhD

The University of Texas Medical Branch,

Department of Otolaryngology,

Grand Rounds Presentation

January 21, 2004