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Skin cancers
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Outline Basal cell carcinoma Squamous cell carcinoma
Cutaneous T-cell Lymphoma Paget’s & Extramammary Paget’s Cutaneous metastases Melanoma
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Basal Cell Carcinoma
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Basal Cell Carcinoma Most common skin malignancy Demographics
Metastasis extremely rare – % locally invasive & destructive Demographics older persons increasing in those <40 Often on sun-exposed areas 85% on head/neck, esp nose Can occur on sun-protected areas
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Basal Cell CA Clinical subtypes: Nodular – most common Pigmented
Sclerosing or Morpheaform Superficial
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Nodular BCC Most common
Pearly, white or pink, telangiectases, rolled borders, center can ulcerate
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Pigmented BCC Brown, blue, or black
Dark-complexioned persons – Hispanics, Asians Borders still pearly with telangiectases DDx: Melanoma
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Sclerosing/Morpheaform BCC
Pale yellow/white, waxy, firm, depressed and scar-like, indistinct borders History of prior cryotherapy Need Mohs or wide excision
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Superficial BCC Least aggressive, but can be difficult to diagnose
Mimic eczema or psoriasis Alcohol swab reveal pearly border + telangiectases
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Treatment Modalities Imiquimod (Aldara):
FDA-approved for superficial BCC little or no scarring, spares tissue variable or unpredictable response Electrodessication & Curettage (ED&C): Best for nodular and small superficial forms Leaves a noticeable scar Best for low risk sites – trunk, extremities
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Treatment Modalities Excision: Mohs micrographic surgery
Offers standard margin check Large long scar Mohs micrographic surgery Tissue sparing procedure Gold standard with 100% margin check Expensive, labor intensive Reserved for: High risk sites Head & neck, shins, hands, tight areas High risk subtypes Recurrent disease Aggressive histology Sclerosing, infiltrating, micronodular, basosquamous
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Squamous Cell Carcinoma
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What is the precursor lesion for squamous cell carcinoma?
Actinic keratosis
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Actinic Keratosis Partial thickness epidermal atypia
Sun exposure, immunosuppressed Erythematous scaly papules, not indurated Smaller lesions often easier felt than seen Can be hypertrophic or even tall (cutaneous horn)
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AK Management Sun protection Cryotherapy – best for isolated lesions
Multiple or extensive lesions: 5-fluorouracil (5-FU/Efudex) Imiquimod (Aldara) Solaraze/Diclofenac – milder reaction than Efudex Chemical peels – pain; wound care Photodynamic therapy (PDT) – pain, minimal wound care, expensive
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Why we treat AKs… 1-5% risk of SCC transformation per year
More likely in hypertrophic AK Suspicious for transformation: Induration Oozing, easy bleeding Recurrent after cryosurgery
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Squamous Cell Carcinoma
2nd most common skin cancer High association UV exposure located mostly on sun-exposed sites scalp, forehead, dorsal nose, superior ears, dorsal hands Prior radiation Marjolin’s ulcer SCC arising on sites of burns, chronic wound/inflammation Immunosuppression (SCC >> BCC) Transplant patients
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Squamous Cell Carcinoma
Scaly papules or plaques with induration, erosion, bleeding May be tender Recurrent after cryosurgery
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Squamous Cell Carcinoma
Local spread can be extensive Follows path of least resistance Subcutaneous & fascial planes, perineural, perichondrium/periosteum, perivascular Treatment similar to BCC except: 4-6 mm margins for standard excision Electrodessication & curettage for small, thin SCC’s in low risk areas
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SCC Metastasis rate: up to 5.2% Lymphatics & hematogenous
Higher risk lesions: Size > 2 cm Depth > 4 mm Aggressive histology Lip or ear location Immunosuppressed Prior XRT Burns or chronic inflammation
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Bowen’s Disease Squamous cell carcinoma in-situ
full thickness atypia Well-demarcated, erythematous, scaly, thin papules/plaques Most common on legs of women & scalp/ears of men Mimic psoriasis or eczema
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Bowen’s Disease Grows slowly, can become invasive SCC Treatment
Small lesions – ED&C, 5-FU, Aldara Large lesions – Excision, 5-FU, Aldara
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Erythroplasia of Queyrat
SCC in-situ of penis or vulva Moist glistening, red, thin plaque (under foreskin) Grows slowly, can become invasive Treatment Aldara or 5-fluorouracil (5-FU) Mohs if around or into urethra
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Keratoacanthoma Smooth dome-shaped nodule with keratin-filled crater
Rapid growth/expansion regresses with scarring
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Keratoacanthoma Considered as a well-differentiated form of SCC
Treatment ED&C, blunt dissection, or excision Intralesional injections 5-FU, Bleomycin, MTX
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Verrucous Carcinoma Exophytic, slow-growing, low-grade SCC
Rarely metastasize Often mistaken for warts Treatment: Excision Avoid XRT, risk of aggressive transformation
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Verrucous Carcinoma 3 subtypes: Buschke-Lowenstein
Genital form HPV 6, 11 Oral florid papillomatosis tobacco chewing poor oral hygiene Epithelioma cuniculatum Plantar feet Older men
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Arsenical Keratoses Discrete round keratoses
Appear 20 yrs after chronic arsenic exposure Most common on palms and soles Not fatal, but may persist indefinitely Pain, bleeding, fissuring, and ulceration Rare in US More common in 3rd world Risk of SCC degeneration
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Cutaneous T-cell Lymphoma
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Cutaneous T-Cell Lymphoma
Malignant T-cells with cutaneous lymphoid antigen (CLA) localize to skin Most common form of CTCL is mycosis fungoides 4 stages Pre-MF Patch Plaque Tumor Prognosis good for first 2 stages then worsens
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Cutaneous T-Cell Lymphoma
Erythroderma can occur in any stage Lesions like persistent eczema/tinea, often sun-protected areas Difficult to diagnose in early stages Average of 6 biopsies before diagnosis made Clinical & histology difficult to distinguish from other inflammatory disorders Monoclonality on T-cell gene rearrangement study is helpful
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Mycosis Fungoides Pre-MF: diagnosis suspected but not proven
Nonspecific pruritis and/or eruption Persists or recurs over months to years Can mimic eczema
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Mycosis Fungoides “Patch” stage: diagnosis possible with histo
Similar morphology pre-MF Poikiloderma vasculare atrophicans: variant of MF
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Mycosis Fungoides Plaque stage: thickening of epidermis
Dusky red-brown plaques with variety of shapes Pruritis can be intense Can remain stable, regress, or progress
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Mycosis Fungoides Tumor stage
may progress from patch or plaque stage lesions or arise de novo Necrosis/ulceration possible
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Mycosis Fungoides Sezary syndrome leukemic form MF Triad: Erythroderma
Lymphadenopathy Sezary cells lymphocytes with cerebriform nuclei
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MF Treatment Patch stage: Generalized lesions
Group I topical steroids, topical nitrogen mustard, Bexarotene (RXR retinoid) Generalized lesions PUVA/UVB Electron beam radiation patch/plaque/tumor most reliable for generalized; high relapse, side-effects Extracorporeal photophoresis Sezary syndrome & erythrodermic MF PUVA of extracted lymphocytes then reinfused into patient
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Paget’s Disease
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Paget’s Disease of the Breast
Invasion of skin from underlying breast cancer Unilateral nipple erythema with serous drainage Appears eczematous, but fixed & indurated with sharp margins
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Paget’s Disease of the Breast
Often confused with eczema of the breast Good diagnostic test: Trial of potent steroid (Lidex or Clobetasol) x 2 weeks If improved or resolved most likely eczema If not need to biopsy to exclude malignancy Treatment: Excision
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Extramammary Paget’s Disease
Usually genital or perianal area Associated with underlying malignancy Location related to internal CA Perianal – GI malignancy Genital – GU malignancy
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Extramammary Paget’s Disease
White-to-red scaling or macerated plaque Often persistent itching or burning Treatment Excision, XRT
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Cutaneous Metastases
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Cutaneous Metastases Usually present as asymptomatic, firm, deep nodules Metastases to skin in 2-10% Most common primaries: Women: Breast (69%) Colon (9%) Melanoma (5%) Ovarian (4%) Men: Lung (24%) Colon (19%) Melanoma (13%) SCC oral cavity (12%)
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Cutaneous Metastases Primary tumors that metastasize to scalp
Thyroid carcinoma (especially papillary carcinoma) Renal cell carcinoma Nodules with alopecia
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Cutaneous Metastases Metastasis to the umbilicus
Sister Mary Joseph’s nodule solitary, firm, fissured nodules represents advanced disease and carries a very poor prognosis Adenocarcinoma of the stomach Adenocarcinoma of the large bowel Ovary Pancreas Endometrium Breast
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Cutaneous Metastases Breast metastasis to skin has variable appearance
Resemble cellulitis Carcinoma en cuirasse hard infiltrated plaque with leathery appearance
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Melanoma
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Melanoma Malignancy of melanocytes May metastasize to any organ
skin >>> eyes, GI tract, and oral/genital mucosa May metastasize to any organ Incidence of melanoma has tripled for Caucasians in the last 40 years Highest incidence in Australia and New Zealand
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Melanoma Accounts for 75% of skin cancer deaths in US
Median age at = 53 years Most common cancer in women aged 25 to 29 Risk factors Family history/genetics People who do not tan or sunburn easily Increased UV exposures and sunburns intermittent UV exposures may be at highest risk
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ABCDE of Melanoma Evolution over time Asymmetry Border irregularity
Goal of this effort is to recognize more melanomas at an early stage Asymmetry Border irregularity Color variation Diameter enlargement Evolution over time
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ABCDE of Melanoma Other factors that should provoke a biopsy:
Erosion or ulceration Scaling Bleeding Loss of normal skin lines Sudden development of pruritus, tenderness, or pain Patient report that “it just feels different”
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Melanoma Types Based upon clinical and histological appearance
Superficial Spreading Lentigo Maligna Nodular Acral Lentiginous
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Superficial Spreading Melanoma
Most common type 4th to 5th decade May develop anywhere on the body Early radial growth Late vertical growth Location: Trunk in men and women Extremities (legs) in women Characterized by variation in color and shape
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Superficial Spreading Melanoma
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Superficial spreading melanoma
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Superficial Spreading Melanoma
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Superficial Spreading Melanoma
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Superficial Spreading Melanoma
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Nodular Melanoma 5th and 6th decade of life 15-20% of melanomas
Males > females May be found anywhere, but more often on the trunk and legs Most commonly dark brown, red-brown, red-black or flesh colored Dome shaped, polypoid or pedunculated Often rapidly growing, friable, ulcerated, and oozing blood
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Nodular Melanoma
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Nodular Melanoma
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Nodular Melanoma
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Lentigo Maligna Melanoma
6th or 7th decade of life 4-15 % of melanomas Most common on the face Extended radial growth phase long period of melanoma-in-situ Vertical growth usually begins in the central portion of the lesion
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Lentigo Maligna Melanoma
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Lentigo Maligna Melanoma
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Lentigo Maligna Melanoma
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Acral Lentiginous Melanoma
Palms, soles, terminal phalanges, mucous membranes 2-8% of melanomas in whites 30-75% of melanomas in more darkly pigmented patients Sudden appearance of a pigmented nail band is suspicious for melanoma
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Acral Lentiginous Melanoma
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Acral Lentiginous Melanoma
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Acral Lentiginous Melanoma
Hutchinson’s sign spread of pigment to the lateral or proximal nail fold in association with nail plate pigmentation
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What do you do with this patient?
Atypical Mole Syndrome and Familial Melanoma
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Atypical Mole Syndrome and Familial Melanoma
Family members with large numbers of atypical moles and tendency to develop thin, superficial spreading melanomas 32,000 patients in the US 5.5% of all melanomas
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Atypical Mole Syndrome and Familial Melanoma
Definition Melanoma in one or more 1st degree relatives More than 50 nevi, with many having atypical appearance Nevi with characteristic histological features 100% lifetime risk of melanoma Remember: Most atypical nevi occur sporadically in people without personal or family history of melanoma
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Atypical Mole Syndrome and Familial Melanoma
Management Refer to dermatology Total body photography Low threshold for biopsy Extensive patient education on: Sun protection Self skin examination Suggest screening of relatives
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Melanoma Evaluation Refer all suspicious lesions to dermatology
Biopsy should include evaluation of deep dermis – we try to avoid shave biopsies Excisional Incisional Punch
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Melanoma Evaluation The most important prognostic factors
Breslow Depth Depth of invasion Measured from granular layer to the deepest invasive component and expressed in millimeter Presence of ulceration upstages the tumor
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Melanoma Evaluation Sentinel lymph node biopsy Other evaluation
indicated for thicker melanoma > 1 mm helpful in staging provides prognostic information identifying those who may benefit from further surgery or adjuvant therapy Other evaluation LFTs Chemistry CBC Imaging studies PET scan and yearly CXR
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Melanoma Management Wide local excision is the primary treatment for melanoma Adjuvant high-dose interferon alpha-2b may be indicated in certain patients Rarely, radiation therapy may be used, especially in LMM Vaccine trials are ongoing
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Melanoma Management Close follow up with history and physical at regular intervals is essential Recurrence may develop up to 10 years after the primary diagnosis Patients with diagnosis of melanoma and non-melanoma skin cancer in the past have increased risk for future melanoma
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Quiz
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Basal cell carcinoma
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Keratoacanthoma
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Lentigo maligna
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Basal cell carcinoma
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Superficial spreading melanoma
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Sister Mary Joseph’s Nodule
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Cutaneous horn
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Nodular melanoma
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Be kind to your skin!
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