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10.1016/j.rmcr.2017.03.006

http://scihub22266oqcxt.onion/10.1016/j.rmcr.2017.03.006
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C5352719!5352719!28337408
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suck abstract from ncbi


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pmid28337408      Respir+Med+Case+Rep 2017 ; 21 (ä): 1-6
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  • Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome) as a differential diagnosis of hypereosinophilic syndromes #MMPMID28337408
  • Santos YAP; Silva BRA; Lira PNZBA; Vaz LCA; Mafort TT; Bruno LP; Lopes AJ
  • Respir Med Case Rep 2017[]; 21 (ä): 1-6 PMID28337408show ga
  • Eosinophilic granulomatosis with polyangiitis (EGPA), formerly known as Churg-Strauss syndrome, is a rare systemic disease situated between primary small vessel vasculitides associated with antineutrophil cytoplasmic antibodies (ANCAs) and hypereosinophilic syndromes (HES). Here, we present a case of EGPA in a 38-year-old male, with a previous diagnosis of asthma, who presented with fever, migratory lung infiltrates and systemic eosinophilia that was refractory to previous courses of antibiotics. This case highlights the importance of the primary care physician understanding the differential diagnosis of pulmonary eosinophilic syndromes.
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