Epidermal Nevi Flashcards

1
Q

Keratinocytic epidermal nevi

A
Involve the SC and stratum malpighii
PI3K, FGFR3
FOXN1 highly expressed
Large lesions of trunk more frequently associated with skeletal
5FU plus 0.1% tretinoin once daily
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2
Q

Nevus comidonicus

A

EEG Abn, IL cataracts and skeletal

FGFR2 (like aperts)

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3
Q

Garcia hafner happle

A

Velvety nonepidermolytic EN
Cerebral defects
fGFR3

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4
Q

Nevus trichilemmocysticus

A

Multiple blaschkoid pilaf cysts

Osteomalacia and fractures

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5
Q

Didymosis aplasticosebacea

A

Nevus sebaceous + ACC in close proximity

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6
Q

SCALP

A

Seb Nevus, CNS malf, ACC, limbal dermoid and pigmented nevus

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7
Q

Gobellos syndrome

A

Systematized velvety orthokeratotic nevus with hypertrichosis and follicular hyperkeratosis

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8
Q

Bafverstedt syndrome

A

Horny excrescences ina linear pattern with MR and sz

Diffuse ichthyosis like hyperkeratosis of the entire body

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9
Q

NEVADA

A

Keratinocytic verrucous epi nevus with angiodysplasia

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10
Q

Hyperkeratosis of the nipple and areola

A

GVHD
AN
Mucocutaneous candidiasis
Sorafenib

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11
Q

High risk of SCC and Bowens from arsenic exposure to what

A

Well water

If from elixirs then higher risk of BCC - latency of 20 years, MC on the scalp

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12
Q

MC site for cutaneous horn

A

Dorsal hands and scalp
May overlie an sk, molluscum, VV, angiokeratoma or trichilemmoma

20% overlie SKs, 20% SCC and 60% benign

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13
Q

KA may be seen

A

With trauma, hypertrophic LP, DLE, tattoos, fraxel, imiquimod, surgical excisions

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14
Q

Subungual KA

A

Don’t regress

Show crescent shaped lytic defect of underlying bone without sclerosis or periosteum rxn

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15
Q

Most definitive histologic finding of KAs

A

Terminal differentiation where the scalloped border of the tumor has lost its infiltrative characteristics and is reduced to a thin rim of keratinizing cells

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16
Q

When to excise KAs

A

When there is not at least 50% involution over 3 weeks

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17
Q

BCC

A

Intermittent sun exposure

18
Q

With 1 BCC what is the risk of another in the next 3 years

19
Q

Pt with BCC have a higher rate malignancy

A

Breast, testicular, and especially NHL

20
Q

BCCs arise from

A

Hair follicle

21
Q

Topical tx of superficial BCC

A

80%, treat for 6 weeks

22
Q

Other mutation in gorlins

A

SUFU with incr susceptibility to meduloblastoma

23
Q

SCC associated with HPV

A

16, 18, 35, 31

24
Q

MC location of EM pagets

25
Risk of underlying malignancy in EMPD
35% (vs 95% in pagets of breast) RCAS1 can be used to monitor invasive dz
26
Hypophasphatemic rickets in epidermal Nevus syndrome
Elevated FGF-23 and MEPE
27
Syringomas
Stain for K5,6,14,16,19,77 on the inner cell layer | K5 and 14 on the outer cell layer
28
Hidrocystomas
Topical atropine or scopolamine cream
29
Syringofibroadenoma (acrosyringeal Nevus of weeden and Lewis)
Hidrotic ectodermal dysplasia | HPV10 has been detected in tumors
30
Mucinous carcinoma
Derived from gland of moll | Express E and progesterone R
31
Curry jones syndrome
Streaky hypopigmentation, hyperpigmented atrophic lines on the soles, multiple trichiblastomas, musculoskeletal, GI, ocular
32
Basaloid follicular hamartoma
Generalized cases associated with alopecia, myasthenia gravis Familial AD dominant form with multiple milia
33
Happle tinschert
Segmental BFH, linear atrophoderma with hypo and hyperpig, IL hypertrichosis, enamel defects
34
EIC of sole
Associated with HPV 60
35
Proliferating pilar cyst
Express K7 | If malignant express CD34
36
Eruptive vellus hair cysts
Ectodermal dysplasia Lowe syndrome Chronic renal failure
37
Drug induced multiple milia
Cyclosporine and 5FU Also naegeli-franceschetti, generalized basilar follicular hamartoma syndrome, gorlins, atrichia with papules, PC type 2, Rombo, BRooke spiegler and basex
38
Milia
Derived from infundibulum
39
Milia en plaque
Mino may tx
40
Auricular pseudocyst
Atopic dermatitis and systemic lymphoma, heavy shoulder carrying, headphones etc
41
MC congenital neck anomaly in children
Thyroglossal duct cyst