| Literature DB >> 32900717 |
Kwee Yen Goh1, Ross Bannon2, Helin Nie Darat2, Bhaskar Ram3, Raghav C Dwivedi2.
Abstract
Granulomatosis with polyangiitis (GPA) is a rare systemic disease of unknown aetiology, characterised by necrotising granuloma formation and diffuse vasculitis. It typically affects the upper and lower respiratory tract in addition to the kidneys. Without treatment, the 2-year mortality rate exceeds 90%. We describe a presentation of intractable serous otitis media, rhinosinusitis, fever and unilateral facial palsy in an 18-year-old man with learning difficulties, which highlights the need for a high index of suspicion in diagnosing and treating this enigmatic disease. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: ear; nose and throat/otolaryngology; respiratory medicine; vasculitis
Mesh:
Year: 2020 PMID: 32900717 PMCID: PMC7477998 DOI: 10.1136/bcr-2019-233685
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X