Literature DB >> 31229976

Corneal melt secondary to eosinophilic granulomatosis with polyangiitis.

Evelyn Fennelly1, Emily Greenan2,3, Conor C Murphy2,3.   

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare antineutrophil cytoplasmic antibody-associated vasculitis that can affect any organ system. It is most often characterised by chronic airway inflammation along with prominent peripheral blood eosinophilia, although the disease can affect the cardiovascular, gastrointestinal, renal or central nervous systems. Ocular manifestations are uncommon and when they do occur, are varied in their clinical presentations. To the best of our knowledge, this is the first case of corneal melt secondary to EGPA to have been reported. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  eye; ophthalmology; respiratory medicine

Mesh:

Substances:

Year:  2019        PMID: 31229976      PMCID: PMC6605890          DOI: 10.1136/bcr-2019-229859

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  33 in total

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