Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report

Granulomatosis with polyangiitis, a type of small-medium vessel vasculitis, can pose diagnostic challenges due to its diverse clinical manifestations. We present a case that mimicked multisystem pyoderma gangrenosum with cutaneous ulceration, renal sparing, and antineutrophil cytoplasmic antibody ne...

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Main Authors: Amanda Gormley, Peter Green
Format: Article
Language:English
Published: SAGE Publishing 2024-12-01
Series:SAGE Open Medical Case Reports
Online Access:https://doi.org/10.1177/2050313X241304229
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author Amanda Gormley
Peter Green
author_facet Amanda Gormley
Peter Green
author_sort Amanda Gormley
collection DOAJ
description Granulomatosis with polyangiitis, a type of small-medium vessel vasculitis, can pose diagnostic challenges due to its diverse clinical manifestations. We present a case that mimicked multisystem pyoderma gangrenosum with cutaneous ulceration, renal sparing, and antineutrophil cytoplasmic antibody negativity. Although antineutrophil cytoplasmic antibody is positive in approximately 90% of cases of granulomatosis with polyangiitis, its negativity should not exclude the diagnosis. Additionally, pyoderma gangrenosum-like cutaneous ulcers should prompt consideration of granulomatosis with polyangiitis, especially in the context of multisystem disease presentation. This case underscores the importance of maintaining a high suspicion for granulomatosis with polyangiitis in patients presenting with cutaneous ulceration and respiratory tract disease.
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spelling doaj-art-ddebdf416be446cbb9ed7075f65348632024-12-11T11:03:26ZengSAGE PublishingSAGE Open Medical Case Reports2050-313X2024-12-011210.1177/2050313X241304229Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case reportAmanda Gormley0Peter Green1Faculty of Medicine, Dalhousie University, Halifax, NS, CanadaDivision of Clinical Dermatology and Cutaneous Science, Department of Medicine, Dalhousie University, Halifax, NS, CanadaGranulomatosis with polyangiitis, a type of small-medium vessel vasculitis, can pose diagnostic challenges due to its diverse clinical manifestations. We present a case that mimicked multisystem pyoderma gangrenosum with cutaneous ulceration, renal sparing, and antineutrophil cytoplasmic antibody negativity. Although antineutrophil cytoplasmic antibody is positive in approximately 90% of cases of granulomatosis with polyangiitis, its negativity should not exclude the diagnosis. Additionally, pyoderma gangrenosum-like cutaneous ulcers should prompt consideration of granulomatosis with polyangiitis, especially in the context of multisystem disease presentation. This case underscores the importance of maintaining a high suspicion for granulomatosis with polyangiitis in patients presenting with cutaneous ulceration and respiratory tract disease.https://doi.org/10.1177/2050313X241304229
spellingShingle Amanda Gormley
Peter Green
Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
SAGE Open Medical Case Reports
title Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
title_full Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
title_fullStr Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
title_full_unstemmed Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
title_short Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
title_sort granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum a case report
url https://doi.org/10.1177/2050313X241304229
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