29- SubQ, Sweat G,Hair, Epith Tumors Flashcards

1
Q

Sharply circumscribed yellow orange hamartoma

Solitary, congenital, linear
Scalp-most common location
Lesions persist through life

A

Nevus sebaceous

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2
Q

Neoplasms that have been described as arising from nevus sebaceous

A

Trichoblastoma

Syringocystadenoma papilliferum

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3
Q

Treatment for nevus sebaceous

A

Surgical removal

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4
Q

Small cream colored/yellowish umbilicated papules

Occurs after age 40
Favors forehead, infraorbital and temples

A

Sebaceous hyperplasia

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5
Q

Prominent sebaceous hyperplasia occurs in 15% of patients taking this drug

A

Cyclosporine

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6
Q

Treatment for sebaceous hyperplasia

A

Purely for cosmetic reasons
Electrosurgery
Laser
PDT

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7
Q

Sebaceous carcinoma is a rare tumor that usually occur on

A

Eyelid or around the eye

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8
Q

This syndrome is now recognized as a subset of the Lynch syndrome/ hereditary nonpolyposis colorectal CA syndrome (HNCCS)

Sebaceous tumor + internal malignancy

A

Muir-Torre Syndrome (MTS)

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9
Q

Most common malignancy associated with MTS and Lynch syndrome

A

Colonic adenocarcinoma

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10
Q

Small papules, yellow, brown or pink
Demonstrates sweat duct differentiation

Frequently occurs on eyelids and upper cheeks

A

Syringoma

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11
Q

Treatment for syringoma

A

Very light electrodessication
Shave removal
CO2 laser

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12
Q

Translucent cystic papules that may have a bluish tint

Eccrine or apocrine differentiation

Solitary, more common in women
Most often periocularly (face or scalp area)

A

Hidrocystoma

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13
Q

Benign slow growing slightly protruding soft sessile reddish tumor that usually occurs on the sole or side of the foot

Bleed on slight trauma
Cup shaped shallow depression from which the tumor grows

A

Poroma

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14
Q

Most common form of sweat duct carcinoma

A

Malignant acrospiroma

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15
Q

Solitary deep seated nodule covered with normal appearing skin

Usually occurs in ventral surface of the body (esp upper half)
15-35 years old
May mets to regional lymph nodes or hema

A

Spiradenoma

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16
Q

This condition may occur with spiradenoma together in the same patient

A

Cylindroma

17
Q

Firm, rubberlike pink-blue tumor that usually occurs on the face and scalp as a solitary lesion

A

Cylindroma

18
Q

Very slow growing plaque or nodule

Head and neck- favor midface and periorbital area, predilection for left side
Upper lip more often than lower

Long term sun exposure msy play a role
Perineural invasion common

A

Microcystic adnexal carcinoma

Sclerosing sweat duct carcinoma

19
Q

Derived from hair matrix cells, bimodal age distribution (1st and 6th decades)

Single lesion on face neck or proximal upper extremity
Asymptomatic, deeply seated firm nodule covered by normal or pink skin
Overlying epidermal atrophy common

A

Pilomatricoma

20
Q

Small dome shaped nodule with a small wisp of fine vellus hairs that protrude through a central pore

Highly structured tumor of the pilosebaceous unit

A

Trichofolliculoma

21
Q

Autosomal dominant
Familial cylindroma or multiple familial trichoepithelioma

Multiple cystic and solid papules on the face
Often symmetrical
Small round smooth shiny slightly translucent firm papules or nodules

A

Brooke-Spiegler syndrome

22
Q

Firm slightly indented (central dell sign) with a raised annular border
skin colored dermal tumor

Affects young women

Focal calcifications, horn cysts and central dell favor this dx

A

Desmoplastic trichoepithelioma

23
Q

Benign neoplasm of follicular germinative cells

Asymptomatic nodules in the deep dermis or subcutaneous tissue, may be pigmented
Scalp most common site, occur in adult

Arise in organoid nevi and represent majority of basaloid neoplasms described as BCC in nevus sebaceus

A

Trichoblastoma

24
Q

Benign neoplasm that differentiates towards cells of outer root sheath

Small solitary papule on the face (nose and cheeks)

A

Trichilemmoma

25
Q

Multiple trichilemmoma may be a marker for this autosomal dominant condition

A

Cowden syndrome

26
Q

Mucocutaneous diagnostic criteria for Cowden syndrome include

TAP the Cow

A

Trichilemmoma
Acral keratoses
Papillomatous papules
Mucosal lesions

27
Q

Mucosal lesions in Cowden Syndrome occur in 80% of patients and usually involve

A

Buccal

Gingival

28
Q

Malignancies associated with Cowden Syndrome

A

Breast
Endometrial
Thyroid

29
Q

Cowden Syndrome is caused by a mutation in this tumor suppressor gene

A

PTEN

30
Q

Smooth compressible cystic mass
Shiny, freely movable
Usually from plugging of follicular orifice, pasty contents cheesy consistency and with pungent odor, may rupture

Usually on face neck and trunk

A

Epidermal inclusion cyst

31
Q

Treatment for epidermal inclusion cyst

A

Surgical excision
β€œDaughter cysts” must be removed- enucleation and scraping with curette

Remove cyst lining- 20%TCA

32
Q

Similar to an epidermoid cyst clinically except that about 90% occur on the scalp

Women over age 60 are predominantly affected and it’s more mobile and firmer than epidermoid cysts

A

Pilar cyst (trichilemmal cyst)

33
Q

This is a large and exophytic neoplasm confined almost exclusively to the scalp and back of the neck.

Up to 25cm in size, more common in women age 65

A

proliferating pilar cyst

34
Q

This occurs in the midline sacral region at the upper end of the cleft of the buttocks

becomes symptomatic during adolescence due to inflammation

Often occurs with nodulocystic acne, dissecting cellulitis and hidradenitis suppurativa

A

Pilonidal cyst

35
Q

Keratinous cysts 1-4mm
White, can occur congenitally (resolve in weeks)

Can also occur due to trauma (chemical peels, dermabrasion, laser), long term use of occlusive moisturizer or topical steroids

A

Milia

36
Q

Treatment for milia

A

Incision and expression of contents :
Blade 11
Cutting tip hypodermic needle
Comedo extractor