Skin and Soft Tissue Flashcards

1
Q

risk factors for melanoma

A

dysplastic/atypical congenital levi (10% lifetime risk for melanoma), familial BK mole syndrome 100% lifetime risk, xeroderma pigmentosum, 10% are familial; fair complexion, easy sunburn, intermittent sunburns, previous skin Ca, previous XRT

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2
Q

where are melanocytes from?

A

neural crest cells in basal layer of epidermis

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3
Q

most common location for distant melanoma metastasis

A

lung

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4
Q

most common metastasis to small bowel

A

melanoma

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5
Q

most common type of melanoma? most aggressive?

A

most common type is superficial spreading melanoma, most aggressive is nodular

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6
Q

recommended margins for melanoma?

A

in situ 0.5-1cm, <1 mm = 1 cm, 1-2mm = 1-2 cm margins, >2mm = 2 cm margins

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7
Q

what is the difference between an in transit lesion and satellite?

A

intransit lesions are > 2 cm from primary lesion but not beyond the nodal basin, satellite lesions are <2 cm

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8
Q

what are the boundaries of a pelvic lymph node dissection

A

superiorly inguinal ligament, medially the fem vessels and adductor longus, laterally sartorius, inferiorly the adductor hiatus

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9
Q

indication for SLNBx in melanoma?

A

for all melanoma >1mm deep or with overlying ulceration regardless of depth

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10
Q

what is an important step for all anterior head/neck melanomas >1mm deep?

A

superficial parotidectomy

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11
Q

most common malignancy in the US?

A

basal cell ca; 4x more common than squamous cell ca

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12
Q

skin bx shows peripheral palisading nuclei and stromal reaction

A

basal cell ca

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13
Q

most common soft tissue sarcoma

A

malignant fibrous histiosarcoma&raquo_space; liposarcoma

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14
Q

staging of sarcoma is based on…?

A

grade

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15
Q

what chemo agents used in sarcoma?

A

doxorubicin based

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16
Q

most common soft tissue sarcoma in children? most common type? worst prognosis?

A

rhabdomyosarcoma; most common type is embryonal (has good prognosis), worst prognosis is the alveolar type

17
Q

CNS tumors, peripheral sheath tumors, pheochromocytoma

A

neurofibromatosis

18
Q

merkel cell carcinoma: features and tx

A

rare neuroendocrine skin ca, pink nodule that progresses to blue color w/ or w/o ulceration, occurs in elderly light skinned pt w/ sun exposure or immunosuppression: AEIOU - asymptomatic, expanding rapidly, immunosuppression, over 50, UV exposed area – Merkel cell polyomavirus, WLE with 1-2 cm negative margins + SLNBx and adjuvant XRT

19
Q

most common location of a desmoid tumor

A

anterior abdominal wall

20
Q

Bowen’s disease?

A

SCCA in situ of perianal margin, 10% turn to invasive SCCA, associated with HPV 16 and 18, tx w/ Imiquimod, cautery ablation, topical 5FU, avoid WLE

21
Q

lab value used in melanoma staging?

A

LDH

22
Q

most common cutaneous soft tissue sarcomas? #1? #2?

A

Kaposi sarcoma > dermatofibrosarcoma protuberans (DFSP)

23
Q

result of the MSLT-1 trial

A

no survival benefit in patients w/ positive SLNBx who underwent completion lymphadenectomy vs observation

24
Q

slow growing soft tissue mass subscapular/infrascapular region: dx, imaging findings, tx

A

elastofibroma dorsi, MRI shows mass w/ streaks of fibrous and fatty tissue located beneath scapula; symptomatic pt undergo simple excision (otherwise observe, no malig potential)

25
Q

which is more common, primary or secondary lymphedema? what’s the most common form of primary lymphedema? what’s the most common form of secondary lymphedema (world? US?)

A

primary lymphedema can be congenital, praecox, and tarda; praecox most common (praecox is primary) accounts for 80-90%, occurs in women; most common worldwide is filariasis, in US most commonly due to post axillary node dissection

26
Q

can you see hyperpigmentation of the skin in lymphedema?

A

usually not, usually due to hemosiderin deposition from venous insufficiencies, not usually w/ lymphedema