Challenges in the Diagnosis of a Case of Granulomatosis with Polyangeitis
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.
© 2021 Daniela Anghel, Elena-Mădălina Hoinoiu, Victoria Iachim, Florentina Vasilescu, Raluca-Anca Bursuc, Elena Busuioc, Valerius Smedescu, Ciprian Viorel Jurcuţ, Cristina-Florentina Pleșa, published by Romanian Society of Internal Medicine
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