| Literature DB >> 16969315 |
Maté Streho1, Régis Sable-Fourtassou, Marie Charlotte Brion, Isabelle Bourotte, Dominique Valeyre, Michel Brauner, Robin Dhote, Sébastien Abad.
Abstract
INTRODUCTION: Churg-Strauss syndrome (CSS) is characterized by asthma, hypereosinophilia, and vasculitis involving at least two extrapulmonary organs. CASE: We report a case of a patient with antineutrophilic cytoplasmic antibody-negative CSS who developed pulmonary interstitial fibrosis (PIF). DISCUSSION: The possible relations between CSS and PIF are discussed. Because this case report is the first to describe features of pulmonary fibrosis in a patient with CSS, we cannot know whether this association is causal or fortuitous.Entities:
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Year: 2006 PMID: 16969315 DOI: 10.1016/s0755-4982(06)74799-6
Source DB: PubMed Journal: Presse Med ISSN: 0755-4982 Impact factor: 1.228