Literature DB >> 9270504

Cutaneous manifestations of Churg-Strauss syndrome: a clinicopathologic correlation.

M D Davis1, M S Daoud, M T McEvoy, W P Su.   

Abstract

BACKGROUND: Allergic granulomatosis of Churg-Strauss (Churg-Strauss syndrome) is a distinct clinical disease of multisystem vasculitis.
OBJECTIVE: We characterize the clinical and histologic features of cutaneous findings in Churg-Strauss syndrome.
METHODS: All patients with Churg-Strauss syndrome seen between 1976 and 1995 were retrospectively reviewed.
RESULTS: Ninety patients with the diagnosis of Churg-Strauss syndrome were identified; 36 (40%) had cutaneous findings. Five patients (6%) had skin lesions as the initial manifestation. The most frequent cutaneous findings were purpura and petechiae on the lower extremities and cutaneous nodules and papules on the elbows. In 37 biopsy specimens from 29 patients, the most common findings were extravascular necrotizing granuloma (15 specimens) and leukocytoclastic vasculitis (16 specimens).
CONCLUSION: Cutaneous lesions in Churg-Strauss syndrome are common. Their characteristic clinical and histologic pattern may help establish the diagnosis.

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Year:  1997        PMID: 9270504     DOI: 10.1016/s0190-9622(97)80125-9

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  12 in total

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Review 7.  [Hypereosinophilic syndrome and Churg-Strauss syndrome: is it clinically relevant to differentiate these syndromes?].

Authors:  B Hellmich; K Holl-Ulrich; H Merz; W L Gross
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8.  Childhood-onset eosinophilic granulomatosis with polyangiitis: a rare childhood vasculitis mimicking anthrax and eosinophilic leukaemia.

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9.  [Eosinophilic granulomatosis with polyangiitis presenting as livedo racemosa].

Authors:  N Klossowski; S Vordenbäumen; P Sewerin; S A Braun; J Reifenberger; B Homey; S Meller
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Review 10.  Cutaneous vasculitis: a rheumatologist perspective.

Authors:  Trinitario Pina; Ricardo Blanco; Miguel A González-Gay
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