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Granulomatosis Polyangiitis Case that Mimics Henoch-Schonlein Purpura

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Date
2019-07-01
Author
KARATOPRAK, CUMALİ
Karaaslan, Tahsin
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Type
Article
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Abstract
Granulomatosis polyangiitis (GPA) is a systemic, necrotizing, granulomatous, antineutrophil cytoplasmic antibody (ANCA) -associated vasculitis that affects small and medium arteries, mainly affecting the upper and lower respiratory tract and the kidneys. It is usually seen over 40 years old. Diagnosis is based on clinical findings, cytoplasmic- C-ANCA positivity and histological findings. Here we report a case of 21-year-old patient who presented with petechial purpuric lesions, abdominal pain, large joint arthritis and hematuria- proteinuria and to whom we started treatment for Henoch-Shonlein Purpura. But a chest imaging showed mass lesion and our final diagnosis was atypical GPA after excluding malignancy, cryoglobulinemia and ANCA related vasculitis in differantial diagnosis.
Subject
Karaaslan T., KARATOPRAK C., -Granulomatosis Polyangiitis Case that Mimics Henoch-Schonlein Purpura-, BEZMIALEM SCIENCE, cilt.7, ss.255-258, 2019
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https://openaccess.bezmialem.edu.tr/handle/20.500.12645/12252
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BEZMIALEM VAKIF UNIVERSITY

About us |Policies | Library | Contact us | Send Feedback | Sitemap | Admin

Bezmialem Vakıf Üniversitesi, Adnan Menderes Bulvarı Vatan Caddesi 34093 Fatih, İstanbul / TURKEY
Copyright © Bezmialem Vakıf Üniversitesi

Creative Commons Lisansı
Bezmialem Institutional Repository, Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır.

OpenAccess@BVU

Support by  UNIREPOS