Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis

Background. Granulomatosis with polyangiitis (GPA) is a small vessel vasculitis characterized by lung and kidney involvement. It is typically a disease of white females and has a poor prognosis with the average life expectancy of 5 months for a patient without treatment. Oral and skin ulcers are con...

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Main Authors: Mohammed Omar Al Salihi, Bianca Dominguez, Viresh Mohanlal, S. J. Carlan
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2022/2737242
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author Mohammed Omar Al Salihi
Bianca Dominguez
Viresh Mohanlal
S. J. Carlan
author_facet Mohammed Omar Al Salihi
Bianca Dominguez
Viresh Mohanlal
S. J. Carlan
author_sort Mohammed Omar Al Salihi
collection DOAJ
description Background. Granulomatosis with polyangiitis (GPA) is a small vessel vasculitis characterized by lung and kidney involvement. It is typically a disease of white females and has a poor prognosis with the average life expectancy of 5 months for a patient without treatment. Oral and skin ulcers are considered to be rare presentations. Case. A 39-year-old black male presented to the hospital with oral and skin ulcers and was diagnosed with GPA based on the biopsies of both cutaneous lesions and kidney. He was started on rituximab with minimal improvement. Later he was admitted to the ICU and had plasmapheresis, and he gradually improved and was discharged home 8 days after admission. Conclusion. GPA is an aggressive vascular disorder resulting in possible organ system damage and failure. The role of the sickle cell trait in this patient is undefined, but this combination of gender, race, and presenting symptoms in GPA is extremely unusual.
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spelling doaj-art-2d24331b71d8480c96699f1d53290e572025-02-03T06:05:02ZengWileyCase Reports in Medicine1687-96352022-01-01202210.1155/2022/2737242Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with PolyangiitisMohammed Omar Al Salihi0Bianca Dominguez1Viresh Mohanlal2S. J. Carlan3Department of Internal MedicineDepartment of Internal MedicineDivision of NephrologyDivision of Academic Affairs and ResearchBackground. Granulomatosis with polyangiitis (GPA) is a small vessel vasculitis characterized by lung and kidney involvement. It is typically a disease of white females and has a poor prognosis with the average life expectancy of 5 months for a patient without treatment. Oral and skin ulcers are considered to be rare presentations. Case. A 39-year-old black male presented to the hospital with oral and skin ulcers and was diagnosed with GPA based on the biopsies of both cutaneous lesions and kidney. He was started on rituximab with minimal improvement. Later he was admitted to the ICU and had plasmapheresis, and he gradually improved and was discharged home 8 days after admission. Conclusion. GPA is an aggressive vascular disorder resulting in possible organ system damage and failure. The role of the sickle cell trait in this patient is undefined, but this combination of gender, race, and presenting symptoms in GPA is extremely unusual.http://dx.doi.org/10.1155/2022/2737242
spellingShingle Mohammed Omar Al Salihi
Bianca Dominguez
Viresh Mohanlal
S. J. Carlan
Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis
Case Reports in Medicine
title Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis
title_full Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis
title_fullStr Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis
title_full_unstemmed Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis
title_short Oral and Lower Extremity Ulcers as the Initial Presentation of Granulomatosis with Polyangiitis
title_sort oral and lower extremity ulcers as the initial presentation of granulomatosis with polyangiitis
url http://dx.doi.org/10.1155/2022/2737242
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AT vireshmohanlal oralandlowerextremityulcersastheinitialpresentationofgranulomatosiswithpolyangiitis
AT sjcarlan oralandlowerextremityulcersastheinitialpresentationofgranulomatosiswithpolyangiitis