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Partha Chakraborty PGT

DEFINITION
Melanocytes of skin & other organs : CNS, eye,

G I tract, G B

Melanocytes : neural crest origin that migrate

during fetal development to above sites, mainly the skin along the basement membrane at the dermoepidermal junction

EPIDEMIOLOGY
Incidence is increasing Whites 45-55 yrs Men > women Men : trunk, head & neck

Women : lower extremities Prognosis better in women

ETIOLOGY
Sunlight : UV rays Both UV A &UV B

UV B

: sunburn, increased melanin UVA : deeper penetration dermal connective tissue damage

RISK FACTORS
High risk (>50-fold increase in risk)

Xeroderma Pigmentosum Persistently changing mole Clinically atypical moles in patient with two family members with melanoma Adulthood (vs. childhood) >50 nevi 2 mm in diameter

Intermediate risk (10-fold increase in risk) Family history of melanoma Sporadic clinically atypical moles Congenital nevi White ethnicity (vs. black or East Asian ethnicity) Personal history of prior melanoma

Low risk (2- to 4- fold increase in risk)

Immunosuppression Sun sensitivity or excess exposure to sun

PRECURSOR LESIONS
Congenital Nevi Dysplastic Nevi

Spitz Nevi
Familial Melanoma

CONGENITAL NEVI
Small :- low risk observation unless local

changes appear Giant:- increased risk complete excision recommended by some authors

DYSPLASTIC NEVI
Large pigmented flat skin lesion with indistinct

margin and variable color Occur sporadically or familial pattern Lack of consensus regarding the management Mostly physician examination 3 to 6 monthly interval with monthly self examination

SPITZ NEVI
Consists of juvenile melanoma, spindle cell

melanoma, epitheloid cell melanoma Rapidly growing, pink or brown benign skin lesions Mostly in children & adolescents Complete local excision :- TOC

FAMILIAL MELANOMA
Age of onset :- earlier Incidence of DNs :- higher Incidence of primary melanoma :- more

common Linked to chromosomes 1p & 9p

THANK YOU

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