Challenges in the Diagnosis of a Case of Granulomatosis with Polyangeitis

Author:

Anghel Daniela1,Hoinoiu Elena-Mădălina1,Iachim Victoria1,Vasilescu Florentina1,Bursuc Raluca-Anca1,Busuioc Elena1,Smedescu Valerius1,Jurcuţ Ciprian Viorel1,Pleșa Cristina-Florentina1

Affiliation:

1. Central Military Emergency University Hospital Carol Davila , Bucharest

Abstract

Abstract Granulomatosis with polyangiitis is a multisystem disease characterized by a necrotizing granulomatous vasculitis, typically associated with the presence of anti-neutrophil cytoplasmic antibodies. The lung is the most common organ involved in comparison to other vasculitis, but in the case presented by us the onset is otorhinolaryngology field, with a multitude of symptoms and immunological tests are initially negative. Over time, immunological tests become positive, but all this leading to a delay in diagnosis by 4 years and of course to a delay in treatment. In this paper we emphasize the usefulness of biopsy for diagnosis and use of anti-neutrophil cytoplasmic antibodies to classify the disease.

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

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