Pigmented Skin lesions Flashcards

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1
Q

where are melanocytes derived from and where do they migrate to

A

derived from neural crest

migrate to skin, uveal tract and leptomeninges

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2
Q

describe the role of the Melanocortin 1 gene(MCR1)

A

encodes MCR1 protein-sits on cell surface, determines balance of pigment in skin and hair, turns phaeomelanin to eumelanin

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3
Q

describe what freckles(ephilides) are

A

patchy increase in melanin pigmentation, reflects clumpy distribution of melanocytes

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4
Q

what are actinic lentigines also known as and what are they related to

A

aka ‘age’ or ‘liver’ spots

related to UV exposure

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5
Q

where are actinic lentigines usually seen

A

face, forearms, dorsal hands

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6
Q

describe the morphology of actinic lentigines

A

epidermis elongated rete ridges, increased melanin and basal melanocytes

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7
Q

what are some of the different types of melanocytic naevi

A

usual type, dysplastic, Spitz, Blue etc.

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8
Q

how common are congenital naevus

A

1-2% babies have them

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9
Q

what are the different sizes for small, medium and large congenital naevus and what is increased risk for large naevus

A

small = <2cm
medium = >2cm <20cm
large= >20cm
10-15% increased risk melanoma

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10
Q

describe development of usual type melanocytic naevus in childhood

A

Junctional naevus = melanocytes proliferate, then form clusters of cells at DEJ

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11
Q

describe the development of usual type melanocytic naevus in adolescence/early adulthood

A

Compound naevus = junctional(DEJ) clusters and groups of cells in dermis

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12
Q

describe the development of usual type melanocytic naevus in adults

A

Intradermal naevus = all junctional activity ceased, entirely dermal

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13
Q

describe the appearance of dysplastic naevi

A

generally >6mm diameter, variegated pigment, border asymmetry

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14
Q

describe the clinical setting of sporadic dysplastic naevi

A

not inherited, one of several atypical naevi, risk of malignant melanoma slightly increased

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15
Q

describe the clinical setting of familial dysplastic naevi

A

strong FH melanoma, autosomal inheritance, lots atypical naevi, lifetime risk melanoma up to 100%

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16
Q

what is the host reaction to dysplastic naevi

A

inflammation and fibrosis

17
Q

how does dysplastic naevi differ to melanoma

A

epidermis not affected in aevi

18
Q

describe what halo naevi are(rare)

A

have a peripheral halo of depigmentation, they show inflammatory regression and are overrun by lymphocytes

19
Q

describe what bleu naevi are(rare)

A

entirely dermal and consist of pigment rich dendritic spindle cells, may have mitosis and mimic melanoma

20
Q

describe what Spitz naevi are(very rare)

A

consist of large spindle and/or epithelioid cells, may closely mimic melanoma, most entirely benign