Glenn D. Goldman, MD. University of Vermont Medical Center. University of Vermont College of Medicine

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Glenn D. Goldman, MD University of Vermont Medical Center University of Vermont College of Medicine

Recognize and identify the main types of skin cancer and their precursors Identify and understand new technological improvements in the treatment of skin cancer Develop a rational approach to diagnosis and management

Increasing incidence w/ more than 1Mil cases per/yr in US Basal Cell Carcinoma 85%-90% Squamous Cell Carcinoma 10%-15% At least 30% of white men in southern USA get skin cancer at some point in their lives Melanoma 1/45 lifetime, Rapid increase

Photoaging: Wrinkling, mottled pigment and onset of actinic keratoses and skin cancer UVB (290-320 nm) Acute sunburn, mutations UVA (320-400 nm) Photoaging, promotion

Premalignant sun induced gritty erythematous macules and keratotic papules - No invasion of dermis May progress to squamous carcinoma Often require destruction with liquid nitrogen or 5-fluorouracil A marker for the potential development of cutaneous malignancy Commonly harbor mutations in p53

Liquid nitrogen cryosurgery Curettage and electrodesiccation 5-fluorouracil Imiquimod Ingenol mebutate Photodynamic therapy

Majority of Skin Cancer Arises from follicular (basal) germ Well over one million cases annually US Indolent but Destructive Doubling time 1 year Rarely metastasizes Locally highly destructive

HEDGEHOG gene pathway Vismodegib Oral medication Dramatic shrinkage of tumors Multiple side effects

250,00 Cases in USA Annually Arises from squamous epithelium Most cutaneous SCC are indolent Rapid Growth Potential Metastasis High risk sites: Ear, Lower Lip High risk lesions: > 2 cm diam. Main risk factor: Sun exposure

Imiquimod Curettage and Electrodesiccation Tangential excision (shave) Standard excision Excision with frozen sections Mohs microscopically-controlled excision Radiation therapy

En face frozen sections: Tissue prepared to show all margins Surgeon is pathologist Almost uniformly w/local anesthesia

All margins evaluated Highest cure rate Tissue Sparing Surgeon as pathologist Surgeon has precise knowledge of tumor location

Literature: Recurrent BCC or SCC, some MIS Morpheaform or micronodular basal cell carcinoma (Aggressive growth) Lesions in the T zone of the face Lesions greater than 2 cm in diameter Facial lesions requiring tissue sparing In practice: Facial skin cancer

The pink is dermis The clear reticular area is subcutaneous fat A small rim of epidermis lines the dermis

Most accurate first cut/section Easy to follow tumor appearance at depth As you cut into the tissue the tumor (BCC) appears

Avoids false positive and false negative depth Generally faster Elegant Less slides Easy to match to defect

Usually local anesthesia No hospital stay Extensive surgery without hospitalization Moderately expensive Very low complication rate

Basal cell and squamous cell carcinoma should be respected as malignancies Early recognition & definitive treatment provide high cure rate & prevent serious deformity and/or death

Malignant tumor of melanocytes Incidence increasing faster than any other maliglancy Current US lifetime incidence approximately 1 in 90 Approximately 7500 deaths in US per year Curable if treated definitively at an early stage

Asymmetry Border Irregularity Color variegation (Multiple shades of brown, black, often red, grey, even blue and white Diameter (Greater than 6 mm) Elevation (Grave prognostic sign)

Overtaking superficial spreading as most commonly diagnosed form of melanoma Long (many years) preinvasive phase as lentigo maligna (melanoma in situ) Peak incidence is in 6 th to 7 th decade By far most common on face

Excision with at least 5 mm peripheral margin Frequently surgical margins are found to be positive, necessitating further surgery Mohs surgery with specialized immunostaining can assist in definitive tumor removal.