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Granulomatosis With Polyangiitis Presenting as Complete Hearing Loss.
Busch, Brandon H; Wilhelm, David; Johnson, Paul; Pfeifer, Mark.
  • Busch BH; Internal Medicine, University of Louisville, Louisville, USA.
  • Wilhelm D; Internal Medicine, University of Louisville, Louisville, USA.
  • Johnson P; Internal Medicine, University of Louisville, Louisville, USA.
  • Pfeifer M; Internal Medicine, University of Louisville, Louisville, USA.
Cureus ; 14(5): e24711, 2022 May.
Article in English | MEDLINE | ID: covidwho-1924622
ABSTRACT
Granulomatosis with Polyangiitis is a rare autoimmune vasculitis that is classically characterized by effects on the upper respiratory tract, lungs, and kidneys. Delay in diagnosis is often attributed to variable and sequential presentation of symptoms rather than concurrent symptomatology. It is important to recognize the wide range of initial presenting symptoms as early diagnosis and treatment is critical in preventing potentially irreversible damage resulting from delayed diagnosis. We present a case of a 29-year-old male with history of mixed sensorineural-conductive hearing loss presumed to be secondary to chronic otitis media who presented to the emergency department with complaint of hematemesis with a subsequent diagnosis of granulomatosis with polyangiitis.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report / Prognostic study Language: English Journal: Cureus Year: 2022 Document Type: Article Affiliation country: Cureus.24711

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report / Prognostic study Language: English Journal: Cureus Year: 2022 Document Type: Article Affiliation country: Cureus.24711