Rheumatology Flashcards

1
Q

Gout Characteristics

A
  1. systemic disease of altered purine metabolism

2. more common in men until women until menopause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Gout Clinical Features

A
  1. initial attack of metatarsal phalangeal joint of greater toe
  2. tophi in chronic gout form adjacent to affected joint
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Gout Diagnostic Studies

A
  1. Joint fluid analysis (rod-shaped, negatively birefringent urate cystals)
  2. uric acid above 8mg/dL
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Non-pharm Gout Treatment

A
  1. elevation and rest

2. dietary modifications (etoh, red meats)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Pharm Gout Treatment

A
  1. NSAIDs (indomethacin)
  2. colchicine
  3. corticosteroid injections
  4. between acute attacks: colchicine, probenacid, sulfapyrazine, allopurinol (not during acute attack), febuxostat
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Calcium pyrophosphate dihydrate (CPPD)/pseudogout general characteristics

A

affects peripheral joints, usually lower extremity, results from intra-articular deposition of calcium pyrophosphate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Pseudogout Clinical Features

A

most common joints are knees, wrist and elbows

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Pseudogout Diagnostic Studies

A
  1. Rhomboid-shaped, positively birefringement crystals

2. linear calcifications (chondrocalcinosis)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Pseudogout Treatment

A
  1. NSAIDs

2. colchicine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

SLE General Characteristics

A
  1. autoimmune disorder characterized by inflammation, positive ANA, involvement of multiple organs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Who does SLE most commonly affect?

A
  1. women of child-bearing age

2. prevalance among familial and ethnic groups (most common in African Americans)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Clinical Features of SLE

A
  1. positive ANA
  2. 4/11 criteria (malar rash, discoid rash, photosensitivity, oral ulcers, arthritis, serositis, renal disease, hematologic, immunologic, neurologic)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Drug-Induced Lupus

A
  1. Histone ANA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

SLE diagnostic studies

A
  1. CBC, BUN, creatinine, UA, ESR, C3/C4
  2. Antibodies to smith antigen, dsDNA
  3. postive ANA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

SLE treatment

A
  1. regular exercise
  2. sun protection
  3. NSAIDs for MSK pain
  4. Antimalarials (hydroxyxholoquine)
  5. corticosteroids
  6. methotrexate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Polymyositis Characteristics

A
  1. inflammatory disease of striated muscle affected the proximal limbs, beck, pharynx
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Dermatomyositis

A
  1. skin manifestation of polymyositis

2. related to underlying malignancies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Clinical Features of Dermatomyositis

A
  1. heliotrope
  2. Grottens Papules (rash on knuckls)
  3. Shawl sign
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Clinical Features of Polymyositis

A

painless muscle weakness

20
Q

Polymyositis Diagnostic Studies

A
  1. elevated CPK/ESR
  2. elevated aldolase
  3. muscle biopsy with myopathic inflammatory changes
21
Q

Polymyositis Treatment

A
  1. High-dose steroids

2. methotrexate/azathioprine

22
Q

Polymyalgia Rheumatica Characteristics

A
  1. 50yo+

2. women more than men

23
Q

Polymyalgia Rheumatica Clinical Features

A
  1. pain/stiffness in the neck, shoulder, pelvic girdles (especially morning)
  2. fever, fatigue, weight loss, depression
  3. MSK symptoms symmetrical, bilateral, proximal
24
Q

Giant Cell Arteritis Clinical Features

A
  1. scalp tenderness
  2. jaw claudication
  3. temporal artery tenderness
  4. BLINDNESS
25
Giant Cell Arteritis Diagnostic
1. Temporal Artery Biopsy
26
Polymylagia Rheumatica Diagnostic Study
1. ESR very elevated
27
Polymylagia Rheumatica Treatment
Low dose steroids (may be required for up to 2 years)
28
Polyarteritis Nodosa Characteristics
1. medium arteries 2. male more than females 3. 40-60yo onset 4. associated with Hep B
29
Polyarteritis Nodosa Clinical Features
1. fever, anorexia, weight loss, abd pain, pripheral neuropathy, arthralgias, arthritis 2. palpable purapura 3. livedo reticularis 4. renal involvement (HTN, edema, oliguria, uremia)
30
Polyarteritis Nodosa Diagnostic Studies
1. ANCA 2. vessel biopsy 3. angiography 4. elevated ESR/CRP and protein uria 5. hep B antibody possible
31
Polyarteritis Nodosa Treatment
high dose steroids
32
Scleroderma (Systemic) Characteristics
1. collagen deposition in skin, heart, lungs, stomach 2. females more than males 3. 30-50yo onset
33
Scleroderma Clinical Features
1. Raynauds 2. collagen depositions 3. puffy hand stage 4. nailfold involvement 5. watermelon stomach, GI dismotility 6. pHTN
34
CREST Clinical features
``` C- calcinosis cutitis R- Raynauds E- esophageal dysfunction S- sclerodactyly (thickening of skin on fingers) T- telanigctasia (dilated small vessels) ```
35
Diagnostic Studies of CREST
+ANA with centromere pattern
36
Diagnostic Studies of SS
1. +ANA (speckled pattern) | 2. anti-SCL-70
37
Scleroderma monitoring
PFT's annually!! screening for phtn
38
Scleroderma Treatment
``` 1. No cure Organ-specific: 2. PPI for reflux 3. ACE inhibitors for renal disease 4. Ca-channel blockers for Raynauds 5. immunosuppresives for pHTN ```
39
Sjogren Characteristics
1. autoimmune disorder that destroys salivary and lacrimal glands 2. could be secondary to to RA, SLE, polyomyostitis, scleroderma
40
Sjogren Clinical Features
1. xerostomia (dry mouth) 2. xerophthalmia (dry eyes) 3. swollen parotid gland
41
Sjogren Diagnostic Studies
1. Shirmer test 2. +RF 3. + ANA 4. anti-Ro antibodies 5. anti-La antibodies 6. lower lip biopsy
42
Sjogren Treatment
Symptomatic 1. pilocarpine (increase salia flow) 2. cyclosporine (ocular sxs)
43
Fibromylagia Characteristics
Central pain diorder
44
Fibromylagia Clinical Features
1. nonarticular MSK aches, pains, fatigue, sleep disturbances, multiple tender "trigger" points 2. fatigue, sleep disruption, mood changes, cognitive disturbances, anxiety, depression, HA, IBS
45
Fibromylagia Diagnostic Studies
exclusion of other dxs
46
Fibromylagia Treatment
1. SSRI 2. TCA 3. Pregabalin (Lyrica) 4. aerobic exercise 5. patient education! (stress reduction, sleep assistance)