Benign epidermal tumors Flashcards

1
Q

When do SK’s start?

A

4th decade of life usually

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2
Q

Genetic mutations associated with seborrheic keratoses?

A

Activating mutations in FGFR3 and PIK3CA

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3
Q

Where don’t SK’s form?

A

Mucous membranes, palms and soles

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4
Q

Are HPV viruses located in SK?

A

SK’s in the genital region are likely condyloma acuminatum. Recommend bx. -HPV has been detected frequently in SK of the groin

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5
Q

What conditions are associated w/ an abrupt appearance/increase in # of SK”s followed by regression when condition resolves

A

Pregnancy, co-existing inflammatory dermatoses (in particular erythroderma), and malignancy.

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6
Q

What cancers are associated with leser-trelat

A

Adenocarcinoma of the breast, colon, gastric and lymphoma

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7
Q

Where is leser-trelat usually seen?

A

On the back, can have itching, can have malignant acanthosis nigracans

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8
Q

What is a lichenoid keratosis?

A

Inflammation/regression of benign lentigo, sk, or ak

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9
Q

What do lichenoid keratoses look like clinically?

A

Pink papule, scaly, most common on the forearm and upper chest (mimics BCC or SCCIS)

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10
Q

What is a path difference between deratosis papulosa nigra and SK?

A

DPN is like an SK w/o the pseudohorn cysts

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11
Q

What virus is stucco keratosis associated with?

A

HPV-23b

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12
Q

How can you get rid of stucco keratosis?

A

Suggest keratolytics

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13
Q

Varients of porokeratosis?

A
  • Porokeratosis of Mibelli
  • Disseminated superficial actinic porokeratosis
  • Linear porokeratosis
  • Punctate porokeratosis
  • Porokeratosis palmaris, plantaris, et disseminata
  • Porokeratotic eccrine ostial and dermal duct nevus
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14
Q

What are the risk factors for porokeratosis that increase the risk of complications, such as malignant transformation?

A

Length of time w/ lesion, older pts, linear variants

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15
Q

Which type of porokeratosis has the lowest risk of malignant change

A

DSAP

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16
Q

What is Flegel’s dz?

A

Hyperkeratosis lenticularis perstans

  • Rare AD, mid to late adulthood -asymptomatic disc-shaped keratotic papules on distal extremities
  • Electron microscopy: absent or altered Odland bodies (lamellar granules) which leads to hyperkeratosis
17
Q

Should you bx cutaneous horns?

A

Yes, in situ or invasive SCC present in up to 20% of lesions.

18
Q

Most common location of clear cell acanthoma?

A

Solitary papule or plaque on leg.

  • Lesions are blanchabe, erythematous, and discrete; they may have attached wafer-like scale at the periphery
  • String of pears of vessels in clear cell acanthoma
19
Q

What is the cause of the clear cells in clear cell acanthoma?

A

Increased glycogen in the cell accounts for their clear appearance and is due to a defect in phosphorylase

20
Q

What is a key feature of IFK compared to SK?

A

Squamous eddies. These are signs that skin has been irritated.

21
Q

What lesion looks like a single spot of darier?

A

Warty dyskeratoma

22
Q

Histology of warty dyskeratoma?

A

Invaginated cup with dyskeratosis and acantholysis

23
Q

What genes are associated with epidermal nevus?

A

FGFR3, PIK3CA, HRAS>NRAS>KRAS

24
Q

DDX for comedones on face?

A

Favre racouchot (old sun-damaged skin, lateral cheeks) , chloracne, nevus comedonicus

25
Q

What do you treat confluent and reticulated papillomatosis with?

A

Oral minocycline (50% success) then could do retinoids

26
Q

Distribution of SK’s usually?

A

Sun-exposed areas, not as apparent on double-clothed areas (areas underwear covers)

27
Q

Clinical presentation of porokeratosis of Mibelli?

A

In kids infancy or childhood usually on distal extremity often several cm in diameter

28
Q

Clinical presentation of disseminated superficial actinic porokeratosis?

A

Onset in middle age, F>M; numerous brownish-red macules w/ keratotic borders on sun-exposed areas (m/c is the legs, rare on the face)

Immunosuppression is a risk factor

29
Q

Clinical presentation of linear porokeratosis?

A

Streaks along the lines of Blaschko: arise during infancy or childhood

Highest risk of progressing to SCC

30
Q

Clinical presentation of punctate porokeratosis?

A

Onset in adolescence; 1-2mm “seed-like” papules on palms and soles

31
Q

When do epidermal nevi typically occur?

A

In the first year of life

32
Q

What is the presentation of porokeratosis palmaris, plantaris, et disseminata?

A

Onset is in childhood/adolescence

  • AD genodermatosis
  • Occurs on the palms/soles initially as uniform hyperkeratotic lesions that look like poro and then involve other areas that are non-sun exposed
33
Q

Clinical presentation of porokeratosis ptychotropica?

A

Red to brown papules and verrucous plaques in the intergluteal cleft on the buttocks

34
Q

What is the clinical description of epidermal nevi?

A

Papillomatous, pigmented, linear plaques along Blaschko’s lines

35
Q

What are the 4 variants of epidermal nevus?

A

Nevus unius lateris: extensive b/l lesions on trunk

Inflammatory linear verrucous epidermal nevus (ILVEN): Along lines of Blaschkow without neurologic defects

Epidermal nevus syndrome: Schimmelpenning syndrome: a/w developmental abnormalitiees (neuro and MSK)

36
Q

What is the clinical presentation of nevus comedonicus?

A

A linear array of comedones on the face>trunk (happens in childhood but worsens during puberty)

37
Q

What genetic abnormalities are involved in nevus comedonicus?

A

FGFR2 mutations: Alagille syndrome, apert syndrome, cardiocranila syndrome, and Crouzon syndrome