NMSC Flashcards

1
Q

Pathophysiology of BCC

A

-inactivation of PTCH tumor suppression gene

-mutations in the patched/hedgehog intercellular signaling pathway

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2
Q

Most common subtype of BCC

A

nodular

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3
Q

First line treatment for BCC

A

standard excision or mohs with 4mm margins

mohs for all high risk BCC

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4
Q

FDA approved use of ED&C for BCC

A

superficial BCCs at non-hair bearing areas and areas that are not high risk

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5
Q

Pathophysiology of SCC

A

mutation of p53 tumor suppression gene

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6
Q

“High Risk” factors of SCC

A
  1. tumor diameter >2cm
  2. poorly differentiated
  3. perineural invasion >0.1mm
  4. tumor invasion beyond fat
  5. bone invasion
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7
Q

transplant organs at high risk for SCC

A

heart and lung

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8
Q

transplant organs at lower risk for SCC

A

kidney and liver

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9
Q

immunosuppressive drug at LOWER risk for skin cancer for transplant patients

A

mTOR inhibitors

-sirolimus (lowest risk)
-everolimus

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10
Q

common risk factor for Merkel Cell Carcinoma

A

polyomavirus infection

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11
Q

Risk factors for Merkel Cell

A

-polyomavirus
-fair skin types
-males 2 fold higher than females
- > 70 yrs old (rare in ppl < 50)
-UV
-Weakened immune system

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12
Q

clinical presentation of merkel cell

A

asymptomatic, firm, nontender solitary rapid growing nodule from 0.5-5cm

pink, violaceous, reddish brown, skin colored

overlying skin intact, may be shiny with telangiectasia or be normal in color

ulceration is uncommon

mostly head and neck region

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13
Q

what should be performed before surgery for all merkel cell patients?

A

CT scan

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14
Q

pathophysiology of b cell lymphoma

A

-nonhodgkin lymphoma
-begins as a reactive inflammatory lymphoproliferative process
-imbalance between apoptosis and cellular proliferation

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15
Q

common predisposing factor of b cell lymphoma

A

chronic stimulation of antigens and infections (viral and bacterial)

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16
Q

risk factors for b cell lymphoma

A

-immunosuppressed (organ transplants, AIDS)
-meds like MTX
-epstein barr virus
-pts receiving chemo/radiation therapy

17
Q

clinical presentation of b cell lymphoma

A

-slow growing
-face, trunk, extremities
-one or multiple smooth red/pink papule/plaque/nodule
-fever, weight loss, night sweats may be present

18
Q

w/u for b cell lymphoma

A

-lymph node exam
-cbc w diff, chemistries, LDH, flow cytometry
-chest x ray and abdominal ultrasound
-CT scan to assess spread (high incidence of spread at time of diagnosis)

19
Q

CTCL poses increased risk for secondary malignancies

which types?

A

-other nonhodgkin lymphomas
-lung
-bladder
-melanoma

20
Q

most common subtypes of CTCL

A

mycosis fungoides

sezary syndrome

21
Q

pathophysiology of CTCL

A

-mutation of T cells in the immune system (malignant T cells) that migrate to the skin

-the malignant T cells in the peripheral blood can cause decrease in healthy CD4+, CD8+, and natural killer cells in the immune system

22
Q

clinical presentation of sezary syndrome

A

-patients advance to atypical lymphocytes (Sezary cells) in their blood and erythroderma of 80-90% BSA
-skin is often erythrodermic and becomes exfoliative
-symptoms are hot, painful, sensitive, and very pruritic skin
-may include hyperkeratosis at the palms and soles, alopecia, onychodystrophy, ptosis, ectropion of the eyelids
-often diffuse lymphadenopathy

23
Q

w/u for CTCL

A

-skin biopsy but hold topical treatments for 2 weeks before biopsy
-labs:
cbc, peripheral smear for atypical serum lymphocytes (sezary cells), LFT’s, BUN, Creatinine, LDH, CD4/CD8
-CXR

24
Q

treatment for limited stage MF CTCL

(patch/plaque stage)

A

-goal is to alleviate symptoms and improve QOL

-topical steroids (clobetasol)

-topical nitrogen mustard (mechlorethamine)

-topical retinoids (bexarotene)

-NB-UVB therapy

-radiation (if localized or solitary tumor)