0071643192.pdf

(Barré) #1

HEMATOLOGY, ONCOLOGY, ALLERGY,


AND IMMUNOLOGY

The ESR is elevated above 50
mm/hr in most patients with
giant cell arteritis. Start
prednisone 1—2 mg/kg/day
immediately to prevent
irreversible blindness.

Drugs That induce
SLE—
HIPPS
Hydralazine
INH
Phenytoin
Procainamide
Sulfonamides

TABLE 9.16. Large Vessel Vasculitis

SYNDROME SIGNS/SYMPTOMS DIAGNOSIS TREATMENT

Giant cell arteritis Involvement of Temporal artery biopsy Prednisone
branches of carotid artery ESR >50 mm/hr
→headache, jaw
claudication, scalp
tenderness, vision changes.

Takayasu’s arteritis Involvement of aorta and Aortic arch arteriogram Prednisone
major branches →finger
ischemia, arm claudication.

TREATMENT
■ NSAIDs for arthritis, arthralgias, serositis
■ Hydroxychloroquine for rash, malaise, arthralgias
■ Steroids for life-threatening manifestations, acute flares, symptoms refrac-
tory to conservative therapy
■ Immunosuppressive therapy

COMPLICATIONS
■ Nephrotic syndrome or renal failure
■ Purulent pericarditis (S. aureus)
■ Pleural effusion/tamponade
■ Interstitial lung disease, pulmonary hypertension
■ Coronary artery vasculitis with acute myocardial infarction
■ Libman-Sacks endocarditis: A noninfectious endocarditis
■ Mesenteric vasculitis

A 70-year-old woman presents with new-onset severe, throbbing, unilat-
eral headache. She has also noted proximal muscle weakness and blurry
vision. Physical exam shows tender, pulseless temporal artery and vision
loss. What’s the suspected diagnosis and next step?
Temporal arteritis (giant cell arteritis). The patient will require immediate high-
dose oral steroids and temporal artery biopsy within 1—2 days.

Vasculitis

Vasculitis is inflammation and necrosis of blood vessels leading to tissue damage.
This may affect different types and sizes of blood vessels. See Tables 9.16, 9.17,
and 9.18.

An infant is status post–cardiac transplant for myocarditis. How might acute
cardiac rejection present?
Feeding intolerance, fever, or fussiness.

The classic case of Henoch-
Schönlein purpura is a boy
between 2 and 11 years old
who presents with palpable
purpura on his legs, edema,
and abdominal pain with a
history of recent URI.
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