« Back to Inflammatory Disorders

Vasculitis

»How are vasculitic disorders defined and classified?
»Are there specific serologic markers for any of these vasculitic disorders?
»What is a leukocytoclastic vasculitis?
»What are some important precipitating causes of small vessel leukocytoclastic vasculitis?
»What is Henoch-Schönlein purpura?
»What is the mnemonic that can help remember the clinical features of Henoch-Schönlein purpura?
»What is “acute hemorrhagic edema of infancy” and how does it differ from Henoch-Schönlein purpura?
»What are cryoglobulins?
»Can cryoglobulins produce a vasculitis?
»What is Churg-Strauss syndrome?
»What were those features again?
»What is Wegener’s granulomatosis?
»What are the features needed to establish a diagnosis of Wegener’s granulomatosis.
»Is there an easy way to remember these diagnostic criteria?
»List the cutaneous findings in Wegener’s granulomatosis.
»Wegener’s granulomatosis and Churg-Strauss syndrome seem very similar. How do you distinguish between them?
»What forms of treatment are available for Wegener’s granulomatosis and Churg-Strauss syndrome?
»What are the major organs involved in classic (systemic) polyarteritis nodosa (PAN)?
»How is classic polyarteritis nodosa different from Kawasaki disease?
»What is primary cutaneous polyarteritis nodosa?
»What is the primary difference between microscopic polyangiitis and PAN?
»What is the difference between giant cell (temporal) arteritis and Takayasu arteritis?
»What is erythema elevatum diutinum?
»Are there any other obscure disorders known to dermatologists, but little known to other subspecialties, that could be classified as vasculitis?

 
 
 

What is a leukocytoclastic vasculitis?


Leukoclastic vasculitis secondary to ampicillin. Typical lesions of palpable purpura are seen.
Fig. 15.1 Leukoclastic vasculitis secondary to ampicillin. Typical lesions of palpable purpura are seen.
Patients with leukocytoclastic vasculitis, also referred to as leukocytoclastic angiitis and allergic or necrotizing vasculitis, present with characteristic purpuric papules, most frequently involving the extremities, known as palpable purpura (Fig. 15-1). Biopsies of cutaneous leukocytoclastic vasculitis demonstrate an intense perivascular infiltrate composed of intact and fragmented neutrophils (nuclear dust) that focally infiltrate the vessel wall producing fibrinoid changes and/or necrosis. These damaged vessels frequently demonstrate extravasation of erythrocytes and may also demonstrate thrombosis.

Kluger N, Francès C: Cutaneous vasculitis and their differential diagnoses, Clin Exp Rheumatol 27(1 Suppl 52):S124–S138, 2009.