Musculoskeletal Flashcards

1
Q

What are the 6p’s of lichen planus?

A
PRURITIC
PURPLE
POLYGONAL
PLANAR
PAPULES
PLAQUES
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2
Q

Lichen planus a blistering skin disorder? Assoc with?

A

No.

Hep C

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3
Q

5 infectious skin disorders?

A
Impetigo
Cellulitis
Necrotizing fasciitis
SSC
Hairy leukoplakia
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4
Q

Define cellulitis

A

Acute, painful, spreading infection of dermis and subcutaneous tissue. Starts from break in skin from trauma or infection

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5
Q

What is impetigo and cellulitis associated with?

A

S. Aureus, s. Pyogenes

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6
Q

3 major skin cancers?

A

SCC
BASAL CELL CARCINOMA
MELANOMA

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7
Q

Cancer assoc with arsenic exposure?

A

SCC

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8
Q

SCC can spread where? Histopath includes what?

A

Spread to lymph nodes.

Keratin “pearls “

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9
Q

What two skin disorders assoc with SCC?

A

Actinic keratosis- scaly plaque and precursor to SCC

Keratoacanthoma- variant that can grow rapidly and regress spontaneously.

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10
Q

Risk of melanoma for metastasis?

What are the ABCDEs?

A

Highly metastatic, Depth of tumor assoc with risk of metastasis.

Asymmetry, border, color, diameter, evolution over time.

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11
Q

What is the tumor marker for melanoma? Associated with what mutation?

A

S-100 tumor marker

Driven by activating mutation in BRAF kinase.

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12
Q

Describe Aspirin mechanism

A

Inhibits cox1 cox2 via covalent acetylation to decrease TXA2 AND prostaglandins. Increase bleeding time for life cycle of platelet (7 days). No effect on pt, PTT. A type of NSAID.

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13
Q

Clinical a dosages for aspirin

A
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14
Q

Toxicities for aspirin?

A

GI ulceration, bleeding. Tinnitus (cn VIII). Reye’s syndrome for kids tx for viral infection. Stimulates respiratory centers can cause hyperventilating and resp alkalosis.

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15
Q

Particular use of indimethacin? What kind of drug is it?

A

Used to close PDA, is an NSAID

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16
Q

Name the 5 blistering skin disorder

A

Pemphigus vulgaris- autoimmune of igG to desmosin
Bulbous pemphigoid- igG to hemidesmosomes
Dermatitis herpetiformis- igA deposits at dermal papillae, associated with celiacs
Erythema multiforme- assoc with mycoplasma pneumonia with, hsv. Look like targets
Steven-Johnson syndrome- associated with adverse drug rxn. 2 membranes involved.

17
Q

Name 2 benign bone tumors

A
  1. Giant cell tumor (soap bubble at epiphysis) 2. Osteochondroma (metaphysis)
18
Q

Name 3 malignant bone tumors

A
  1. Ewing Sarcoma (diaphysis) 2. Chondrosarcoma (diaphysis) 3. Osteosarcoma “Codman triangle (Metahpysis)
19
Q

Compare contrast osteoarthritis and rheumatoid arthritis

A

O is mechanical due to age, obesity, trauma, joint deformity. Pain in weight-bearing joints with improvement after use. Tx NSAIDS, glucocorticoids. RA is autoimmune due to inflammation and destruction of synovial joints. Pannus formation, ulnar deviation of fingers. Tx NSAIDS, gluccocorticoids , TNF-alpha inhibitors.

20
Q

Sjogren syndrome. Autoimmune or mechanical? Symptoms.

A

Autoimmune due to destruction of exocrine glands (lacrimal/salivary). Xeropthalmia (decreased tear production), xerostomia, bilateral parotid enlargement.

21
Q

Describe polymyositis and dermatomyositis

A

Polymyositis- symmetric proximal muscle weakness due to inflammation of CD8 T cells. Dermatomysositis- similar to polymyositis including malar rash (seen in SLE), shawl and face rash. Tx steroids.

22
Q

Define Myositis ossification

A

Metaplasia of skeletal muscle to bone following muscular trauma.

23
Q

Define scleroderma

A

Excessive fibrosis and collagen deposition throughout the body. Leads to puffy and taught skin.

24
Q

Define CREST ( a type of scleroderma)

A

CREST: Calcinosis, Raynaud phenomenon, Esophageal dysmotility, Sclerodactlyly, Telangiesctasia.

25
Q

Describe RA

A

Autosomal disorder with genetic predispositions for HLA-DR4 or switching of arginine to citrulline.

Clinical Presentation: effecting small joints (not DIP), morning stiffness, pannus formation (fibrous granulation tissue in joints), cervical spine involvement
Labs: anti-citrulline antibodies.