Chapter 61- Vasculitis Flashcards

0
Q

What are the diseases that hypersensitivity vasculitis is associated with?

A

Rheumatoid arthritis
SLE
Bacterial endocarditis
Chronic infection with HCV(b/c causes essential mixed cryoglobulinemia)

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1
Q

What are the different vasculitis?

A
Polyarteritis nodosa
Wegener granulomatosis
Takayasu arteritis
Temporal arteritis
Churg-strauss disease
Hypersensitivity vasculitis (henich-Schönlen purpura)
Microscopic polyangitiis
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2
Q

Chronic hepatitis B and C are associated with teo types of vasculitis, what are they?

A

Microscopic polyangitiis and polyarteritis nodosa

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3
Q

What are the hx and PE findings for wegener granulomatosis?

A

HX-> hemoptysis, cough, dyspnea, recurrent sinusitis

PE-> HTN, palpable purpura, septal ulceration, saddle-nose

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4
Q

What are the findings for polyarteritis nodosa in Hx and PE?

A

Hx-> nothing specific, general symptoms of fever, weight loss, malaise and arthralgia
PE-> HTN, palpable purpura

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5
Q

What are the Hx and PE findings of churg-strauss disease?

A

Hx-> general sx of fever, malaise, wieght loss and arthralgias. Also recurrent asthma attacks.
PE-> CHF, purpura most common in churg-strauss disease compared to the other vasculitis

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6
Q

What are the findings in Hx and PE for hypersensitivity vasculitis?

A

Hx-> fever, malaise, weight loss, arthralgias, for henich-schölein purpura : abdominal pain before rash,
Pe-> often skin involvement is the only system involved, rashes are very common, HTN,

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7
Q

What are the Hx and PE findings for temporal arteritis?

A

Hx-> new onset headache, scalp tenderness, jaw claudication

PE-> tender and thickened temporal arteries

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8
Q

What are the hx and pe findings for takayasu arteritis?

A

Hx-> syncope, stroke

PE-> diminished peripheral pulses (pulseless)

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9
Q

What are the hx and pe findings in microscopic polyangitiis?

A

Hx-> general findings of vasculitis

Pe->

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10
Q

Pe findings in vasculitis (general ones)?

A

Mononeuritis multiplex, cranial nerve palsies, palpable purpura, skin rashes,

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11
Q

Bx findings in vasculitis

A

Granuloma-> churg-strauss (with eosinophils), WG and temporal arteritis
Mononuclear cell or PMN + necrotizing-> polyarteritis nodosa, microscopic polyangitiis
Leukocytoclastic vasculitis-> hypersensitivity vasculitis (in henoch-schölein purpura you have IgA)

Takayasu -> usually dont bx

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12
Q

Ddx of palpable purpura for vasculitis?

A

Disseminated meningococcal, gonococcal or rocky mountain spotted fever

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13
Q

What other etiology is important to consider when pt presenting with fever, skin lesions and weight loss?

A

Subacute bacterial endocarditis

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14
Q

Eosinophilia and pulmonary inflitrates are characteristic for churg-strauss disease yet, you need to make sure it is not….(3)

A

Allergic bronchopulmonary aspergilliosis, loeffler syndrome, chronic eosinophilic pneumonia.

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15
Q

Pulmonary + renal disease are strongly aa with WG but make sure it is not…

A

Goodpasterur syndrome

16
Q

Explain the diagnostic evaluation for vasculitis.

A
  1. Blood test: increased ESR (>100mm per hour), normocytic & normochromic anemia, thrombocytosis, leukocytosis (* bacterial), high eosinophil (think churg-strauss although also possible in hypersensitivity vasculitis)
  2. CXR-> WG will have nodules and cavitation, churg-strauss also has findings of pulmonary infiltrates.
  3. Blood culture when suspecting bacterial infection.
  4. Serology testing:
    - C-AMCA: WG
    - P-ANCA: WG, microscopic polyangitiis and churg-strauss disease.
    - rheumatoid factor: rheumatoid vasculitis, mixed cryoglobulinemia
    - hepatitis c antibody: mixed cryoglobulinemia
    - hepatitis b antibody: polyarteritis nodosa
  5. Biopsy
  6. Angiogram
    - Polyarteritis nodosa: mesenteric vessels will show beaded appearance of aneurysm with segmental stenosis
    - takayasu arteritis: irregular wall of aorta and subclavian arteries
  7. MRI to dx and follow takayasu arteritis
17
Q

List the different treatments for every type of vasculitis.

A

Polyarteritis nodosa: prednisone (6 mo) + cyclophosphamide (1yr)
Wegener granulomatosis:prednisone + cyclophosphamide. Plasma exchange in severe cases.
Microscopic polyangitiis: prednisone + cyclophosphamide
Takayasu arteritis: steroids, methotrexate and sx grafting
Temporal arteritis: prednisone
Churg-strauss disease: prednisone
Hypersensitivity arteritis, esp. Henoch-schölein purpura: can resolve but it doesn’t, prednisone.

Cyclophosphamide can be replaced by methotrexate and azathioprine after 3-6 mo of administration in order to avoids complications (hemorrhagic cystitis, bladder cancer, myelodysplasia and infertility)of this one.