Rheumatology/MSK Flashcards

(61 cards)

1
Q

What is primary biliary cirrhosis?

A

Pruritis, xanthomas, anti-mitochondrial Ab; seen in females

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2
Q

What is primary sclerosing cholangitis?

A

P-ANCA Ab, bike duct inflammation, onion skinning, IBD

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3
Q

What is type I autoimmune hepatitis?

A

Anti-smooth mm. Ab; seen in young women

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4
Q

What is type II autoimmune hepatitis?

A

Anti-LKM Ab

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5
Q

What is bullous pemphigoid?

A

Anti-hemidesmosome Ab, subepithelial skin bullae

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6
Q

What is celiac sprue?

A

Anti-gliaden Ab (can’t eat wheat/ bread products = steatorrhea) assoc. w/ dermatitis herpetifomis

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7
Q

What Ab is assoc. w/ CREST Syndrome?

A

Anti-centromere Ab

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8
Q

What is dermatitis herpeteformis?

A

Vesicles on anterior thigh, Anti-BMZ Ab, Anti-endomysial Ab

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9
Q

What is dermatomyositis?

A

Anti-jo-1 Ab; Myositis with a rash; Assoc. w/ occult malignancy

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10
Q

What are symptoms of T1DM?

A

Polyuria, polydipsia, wt. loss, Anti-islet cell Ab, anti-GAD Ab, post-infection, DKA

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11
Q

What is drug Induced lupus(and causative drugs)?

A

Anti-histone-Ab;

Drugs:
Hydralazine 
Isoniazid 
Phenytoin
Penicillamine
Procainamide
Ethosuximide
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12
Q

What is gastritis type A?

A

Anti-parties cell, an strophic gastritis adenocarcinoma

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13
Q

What is goodpasture’s?

A

Anti-GBM Ag, attacks the lungs and kidneys, can progress to RPGN and death

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14
Q

What is Graves’ disease?

A

Anti-TSHr Ab, hyperthyroid exopthalmos, pretibial myxedema

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15
Q

What is Hashimotos?

A

Anti-microsomal Ab/anti-TPO, hypothyroid

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16
Q

What is ITP (immune thrombocytopenic purpura)?

A

Anti-platelet Ab, anti-GP IIB/IIIA Ab

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17
Q

What is MCTD (mixed connective tissue disease)?

A

Anti-RNP Ab

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18
Q

What is mononucleosis?

A

Heterophile Ab positive; teenager w/ sore throat, lymphadenopathy, splenomegaly, “kissing disease”

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19
Q

What is MPGN type II?

A

Anti-C3 convertase Ab= C3 nephritic factor

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20
Q

What is paroxysmal hemolysis?

A

Donate landsteiner Ab; bleed when cold

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21
Q

What is pemphigus vulgaris?

A

Anti-desmosome Ab (skin sloughs off when touched) starts in oral mucosa

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22
Q

What is pernicious anemia?

A

Anti-IF Ab, via. B12 deficiency = megaloblastic anemia

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23
Q

What is polyarteritis nodosa?

A

P-ANCA Ab; attacks gut, kidneys and nervous system; assoc. w/ Hep. B infection. There is no pulmonary environment

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24
Q

What is post-strep. GN?

A

ASO Ab, Nephritic w/ complement deposition; after 3 weeks post-infection

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25
What is RA?
Rheumatoid factor present pain and swelling, worse in the morning, anti-citrullinated peptide protein Ab's
26
What is scleroderma?
Anti-Scl70 Ab (anti-Topol), fibrosis, tight skin, masked faces
27
What is Sjogrens?
Anti-SSA Ab, dry eyes, dry mouth, arthritis
28
What is SLE?
Anti-dsDNA; Anti-Smith, Anti-cardiolipin Ab. | Malar rash, photosensitivity, oral ulcers, RF positive, VDRL positive but not infected, FTA-ABS to confirm
29
What is SLE Cerebritis?
Anti-neuronal Ab; Anti-ribosomal Ab
30
What is Vitiligo?
Anti-melanocyte Ab; white patches on skin
31
What is warm hemolysis?
Anti-Rh Ab; bleeds at body temperature
32
What is Wegner's?
c-ANCA Ab; attacks ENT, Lungs, and kidney
33
What is HSP?
IgA Disease - 2 or 3 days post-common cold or GI infection. Leads to Berger's
34
What is Berger's?
IgA disease, 2 weeks post vaccination; serum sickness
35
What is Alport's?
IgA disease; 2 weeks after diarrhea, HSP and polio
36
Where is CK-MB found?
Heart
37
Where is CK-MM found?
Muscle
38
Where is CK-MB found?
Brain
39
Why should you wait 30 mins after a meal before swimming?
All blood is shunted to GI for digestion, digestion depletes ATP stores; No ATP = no muscle movement
40
How does neurogenic muscle disease present?
Distal weakness and fasciculations
41
How does myopathy muscle disease present?
Proximal weakness and pain
42
What is a light chain composed of?
Actin
43
What is a heavy chain composed of?
Myosin
44
What band of sarcomere does not change length?
The A band
45
Where are T-tubules located?
Cardiac mm: at the z-line | Skeletal mm: at the A-I junction
46
What is duchenne's muscular dystrophy?
Caused by a dystrophin frame shift; defective Dystrophin patient will have a Gower sign and calf pseudohypertrophy
47
What is Becker Muscular Dystrophy?
Dystrophin Missense; milder form of DMD | Symptoms present after 5yo
48
What is seen with Myotonic Dystrophy?
Bird's beak Face; can't let go when shaking hands
49
What is Myasthenic Syndrome/Lambert-Eaton?
Patients will tell you that they get stronger as the day goes by; stronger with EMG (electromyography) Assoc. w/ small cell CA
50
What is Myasthenia Gravis?
Anti-ACh post-synaptic Ab; PT ~20-30yo, weaker as day goes on (dysarthria, ptosis, dysphagia) Periotic exacerbations get stronger w/ Edrophonium Weaker with EMG (electromyography); must rule out thymoma
51
What is MS?
Production of Anti-myelin Ab MC in 20-40yo women, vision disturbances, spasticity (UMNs), decreased sensation, symptoms wax and wane - each MS attack gets worse
52
What is Metachromatic Leukodystrophy?
Arylsulfatase A deficiency; a child who presents similar to MS
53
What is ataxia telangiectasia?
IgA deficiency; PT has spider veins
54
What do you see in Friedrick's Ataxia?
Retinitis pigmentosa, scoliosis
55
What is adrenal leukodystrophy?
Carnitine acyltransferase (CAT-1), defective adrenal failure (XR); long-chain FA stuck in cytoplasm
56
What is Guillain-Barre?
Ab's damage multiple peripheral nerves (acute inflammatory polyneuropathy); patients present with ascending paralysis 2 weeks post-UTI
57
What is ALS?
Descending paralysis seen in middle aged men with fasciculations; no sensory problems
58
What is Werdnig-Hoffman?
Fasciculations in newborn due to failure of anterior horns to develop
59
What is polio?
Asymmetric fasciculations in kids; presents 2 weeks post- gastroenteritis
60
What is choreoathetosis?
Dance-like movements; wringing of hands, quivering/unsteady voice
61
What is Atonic Cerebral Palsy?
No mm. Tone - floppy