| Literature DB >> 28065613 |
Klearchos Psychogios1, Ilias Evmorfiadis2, Spyros Dragomanovits3, Athanasios Stavridis4, Konstantinos Takis4, Loukas Kaklamanis5, Pantelis Stathis4.
Abstract
Eosinophilic granulomatosis with polyangiitis (EGPA, previously named Churg-Strauss syndrome) is a form of necrotizing vasculitis occurring in patients with asthma and eosinophilia. Ischemic stroke is a relatively rare complication of the disease. We report a case of a 63-year-old woman with multiple embolic infarcts, hypereosinophilia (for >7 years), and skin rash. Elevated cardiac enzymes and cardiac magnetic resonance imaging were consistent with endomyocarditis. The simultaneous presence of history of asthma, sinusitis, hypereosinophilia, and vasculitis led to the diagnosis of EGPA. This case contributes to the recent debate of the 2 possible presentations of the disease according to the ANCA (antineutrophil cytoplasmic antibodies) status. We furthermore underscore the need for careful differential diagnosis of the "ANCA negative" cases with persistent hypereosinophilia from the idiopathic hypereosinophilic syndrome.Entities:
Keywords: Churg–Strauss syndrome; Stroke; hypereosinophilia; vasculitis
Mesh:
Year: 2017 PMID: 28065613 DOI: 10.1016/j.jstrokecerebrovasdis.2016.12.009
Source DB: PubMed Journal: J Stroke Cerebrovasc Dis ISSN: 1052-3057 Impact factor: 2.136