Rheumatology/MSK Flashcards

(51 cards)

1
Q

What is Primary Biliary Cirrhosis?

A

Seen in females, pruritus, xanthomas, anti-mitochondrial antibody

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2
Q

What is Primary Sclerosing Cholangitis?

A

p-ANCA antibody, bile duct inflammation, onion skinning, IBD

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3
Q

What is Type I Autoimmune Hepatitis?

A

Seen in young women, anti-smooth muscle Ab

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4
Q

What is Type II Autoimmune Hepatitis?

A

Seen in kids, Anti-LKM Ab

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5
Q

What is Bullous Pemphigold?

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, Associated with Dermatitis Herpetiformis

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7
Q

What antibody is associated with CREST Syndrome?

A

Anti-Centromere Ab

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8
Q

What is Dermatitis Herpetiformis?

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, Associated with occult malignancy

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10
Q

What is DM Type 1?

A

Polyuria, Polydipsia, weight loss, Anti-Islet cell Ab, Anti-GAD Ab, post infection, DKA

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11
Q

What is Drug Induced Lupus?

A

Anti-Histone Ab “HIPPPE” drugs cause this. H – Hydralazine, I – INH, P – Phenytoin, P – Procainamide, P – Penicillamine, E - Ethosuximide

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12
Q

What is Gastritis Type A?

A

Anti-Parietal cell, an Atrophic Gastritis Adenocarcinoma

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13
Q

What is Goodpasture’s?

A

Anti- GBM Ab, attacks the lung and kidney, can progress to RPGN and death

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14
Q

What is Grave’s Disease?

A

Anti-TSHr Ab, Hyperthyroid, Exophthalmos, Pretibial Myxedema

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15
Q

What is Hashimoto’s?

A

Anti-Microsomal Ab / anti-TPO Hypothyroid

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16
Q

What is ITP (Immune Thrombocytopenic Purpura)?

A

Anti-Platelet Ab Anti - GP2b3a Ab Thrombocytopenia

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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 with 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

Donath Landsteiner Ab, (they bleed when they are cold)

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21
Q

What is Pemphigus Vulgaris?

A

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

22
Q

What is Pernicious Anemia?

A

Anti-IF Ab, vitamin B12 deficiency = Megaloblastic Anemia

23
Q

What is Polyarteritis Nodosa?

A

p-ANCA Ab, attacks the gut kidneys and nervous system, associated with Hep B infection, there is no pulmonary environment

24
Q

What is Post-Strep GN?

A

ASO Ab, Nephritic with complement deposition, after 3 weeks post infection

25
What is Rheumatoid Arthritis?
Rheumatoid factor present pain and swelling is worse in the morning, anti-citrullinated peptide protein antibodies
26
What is Scleroderma?
Anti-Scl70 Ab, (Anti-TopoI) fibrosis tight skin, masked faces
27
What is Sjogrens?
Anti-SSA Ab, dry eyes, dry mouth, arthritis
28
What is SLE?
Anti-ds DNA / Sm / Cardiolipin Ab, Malar Rash, photosensitivity, oral ulcers, rheumatoid factor positive, VDRL test 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-BB found?
Brain
39
Why should you wait 30 minutes after a meal before swimming?
All blood is shunted to the GI for digestion, digestion depletes ATP, stores No ATP = No muscle movement
40
How does a Neurogenic Muscle Disease present?
Distal weakness and fasciculation’s
41
How does a Myopathic 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 the Sarcomere does not change length?
The A Band
45
Where are the T-Tubules located?
Cardiac Muscle: At the Z line, Skeletal Muscle: At the A-I Junction
46
What is Duchenne's Muscular Dystrophy?
Caused by a Dystrophin Frameshift Defective Dystrophin, patients will have a Gower sign and calf Pseudohypertrophy
47
What is Becker's Muscular Dystrophy?
Dystrophin Missense, milder form of DMD, symptoms present after 5 years of age.
48
What is seen with Myotonic Dystrophy?
Bird's Beak Face, can't let go when they shake hands
49
What is Myasthenic Syndrome?
Patients will tell you they get stronger as the day goes by, stronger with EMG, Is associated with small cell CA - Lambert-Eaton Syndrome
50
What is Myasthenia Gravis?
Anti-ACH postsynaptic Ab, patients between approximately 20-30 years old get weaker as the day goes by (dysarthria, Ptosis and dysphagia), periotic exacerbations get stronger with Edrophonium, weaker on EMG, must rule out Thyoma
51
What is Multiple Sclerosis?
Due to production of Anti-Myelin antibody, Seen more common in 20-40 year old women, complain of vision disturbances, spasticity (UMN), decreased sensation, symptoms wax and wane - each MS attack gets worse