Rheumatology Flashcards

1
Q

Differential dx of monoarthritis (list 8)

A

Trauma
Infection
- Acute: septic arthritis, osteomyelitis
- Chronic: remember TB and Lyme!
Inflammatory: transient synovitis (short duration), JIA
Tumor: localized bone tumor
Hemarthrosis: consider bleeding disorder (vWD, hemophilia)
Mechanical/orthopedic: overuse (ex. Osgood-Schlatter), AVN, SCFE, Chondromalacia patellae (patellar femoral syndrome)
Pain syndrome: conversion, CRPS

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2
Q

Which organisms cause septic arthritis?

A
staphylococcus aureus
Streptococcus pneumoniae
Haemophilus influenza
GBS
E.coli
Nisseria Gonorrhea
Kingella Kingae
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3
Q

Describe the synovial fluid seen in septic arthritis

A

Synovial fluid WBC count > 50,000 (mostly neutrophils)

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4
Q

Kocher criteria?

A

fever > 38.5
ESR > 40 mm/hr
WBC > 12,000
refusal to weight bear

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5
Q

Basic labs required for febrile child with joint pain

A

CBC and differential, CRP, ESR, blood culture

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6
Q

Stages of Lyme disease, and their characteristics

A

o Early localized Lyme (< 30 days): erythema migrans + may have systemic symptoms, including arthralgia. Clinical diagnosis
o Early disseminated Lyme (skin – multiple EM, neuro – facial nerve palsy, meningitis, carditis – AV block, joints – migratory arthralgias).
o Late disseminated Lyme (4-6 weeks later): chronic intermittent arthritis, - usually monoarthritis of the knee; peripheral neuropathy, encephalomyelitis

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7
Q

List 6 clinical criteria of SLE

A
  • Acute cutaneous lupus (lupus malar rash; bullous lupus; TEN variant of SLE; photosensitive lupus rash or subacute cutaneous lupus)
  • Chronic cutaneous lupus (discoid lesions local and generalized)
  • Oral or nasal ulcers
  • Non-scarring alopecia
  • Arthritis
  • Serositis (pleurisy or pulmonary effusion or pericardial pain or pericardial effusion or rub or pericarditis)
  • Renal (urine protein to Cr 500mg/24 hours or red blood cell casts)
  • Neurologic (seizures, psychosis, peripheral or cranial neuropathy, acute confusional state)
  • Hemolytic Anemia
  • Leukopenia or lymphopenia
  • Thrombocytopenia
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8
Q

List 4 immunologic criteria of SLE

A
  • ANA
  • Anti-DNA (specific)
  • Anti-Sm
  • Antiphospholipid antibody (lupus anticoagulant, false positive RPR, antiocardiolipid)
  • Low complement (C3, C4)
  • Direct Coombs test
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9
Q

Xray findings seen in JIA

A

soft tissue swelling and periarticular osteopenia; later narrowing of joint spaces, bone cysts, erosions, subluxations, ankylosis

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10
Q

Side effects of NSAIDS (list 5)

A

gastritis, headaches, dizziness, fatigue, hepatitis, nephrotoxicity (proteinuria or renal papillary necrosis), friability of skin, Reye syndrome

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11
Q

Cardiac complications of JIA

A

pericarditis, myocarditis (in systemic onset JIA)

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12
Q

Anterior uveitis most commonly occurs in which subtype of JIA?

A

oligoarticular JIA, ANA+

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13
Q

Diagnostic criteria of HLH/MAS

A

Initial diagnostic criteria:

  • Fever
  • Splenomegaly
  • Cytopenias
  • Hypertriglyceridemia and/or hypofibrinogenemia
  • Hemophagocytosis in bone marrow or spleen or lymph nodes (no evidence malignancy)

New diagnostic criteria:

  • Low or absent NK cell activity
  • Increased Ferritin greater/equal 500 mg/L (>10,000 is sensitive and specific)
  • Elevated soluble CD25
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14
Q

Diagnostic criteria for Kawasaki disease

A
Fever > 5 days
and at least 4/5 of:
- conjunctivitis
- rash
- adenopathy
- extremity changes
- oromucosal changes
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15
Q

List 5 items in the DDx of Kawasaki disease

A
  • Viral infections: measles, echovirus, adenovirus
  • Toxin mediated illnesses: Toxic shock syndrome (strep, staph), scarlet fever (group A strep)
  • Drug reactions: Steven Johnson syndrome, serum sickness
  • Systemic-onset JIA
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16
Q

Supplemental lab criteria for incomplete KD

A

If fever> 5 days, and 2-3 clinical criteria, ESR > 40, CRP > 3:

  • Albumin < 3 g/dl
  • Anemia for age
  • Elevated ALT
  • Platelets > 450,000 per mm3
  • WBC > 15, 000
  • Urine > 10 WBC/hpf
17
Q

Cardiac complications of Kawasaki

A
  • Coronary artery aneurysms (independent RF = male gender, delay of treatment > 10 days and IVIG retreatment)
  • KD shock syndrome
  • Myocarditis (prolonged PR, nonspecific ST and T wave changes)
  • Reduced LV function and contractility
  • CHF, valvulitis
  • pericardial effusion or tamponade
  • MI, coronary artery thrombosis, sudden death
  • Vascular obstruction (thrombolysis then heparin)
18
Q

Clinical features of JDM (Juvenile dermatomyositis)

A

• Phase 1: Prodromal phase: nonspecific aches and pains, low grade fever, edema hands/feet/eyelids, diffuse non-specific rash
• Phase 2: progression muscle weakness and rash (violaceous heliotrope rash, Gottron papules over extensor tendons, periungual erythema)
o Proximal muscle weakness
• Phase 3: persistent active disease and cumulative tissue damage
• Phase 4: indolent phase with contracture, muscle wasting, lipodystrophy, pigmentary changes and calcinosis

19
Q

List systemic complications of polyarteritis nodosa

A

Cardiac: pericarditis, cardiomegaly
CNS: seizures, hemiparesis
GI: gut vasculitis
Pulmonary: diffuse infiltrates, pulmonary hemorrhage, hemothorax
Renal: proteinuria, urine sediment, HTN
Arthritis, livedo reticularis, urticarial, petechial rashes

20
Q

List 5 complications of JDM (juvenile dermatomyositis)

A
  • skin calcinosis
  • proximal muscle weakness
  • resp insufficiency (diaphragm weakness)
  • contractures
  • heliotrope rash
  • Gottron papules
  • GI bleed, perforation