Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis
Mucormycosis is a rare but fatal disease caused by a filamentous fungus involving the nose, paranasal sinuses, and brain. These organisms usually cause severe infections in immunocompromised individuals. Granulomatous polyangiitis (GPA), also known as Wegner’s granulomatosis, is a rare, aseptic necr...
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Language: | English |
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Wiley
2023-01-01
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Series: | Case Reports in Infectious Diseases |
Online Access: | http://dx.doi.org/10.1155/2023/7934700 |
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author | Syeda Aasia Batool Usha Kumari Salim Surani |
author_facet | Syeda Aasia Batool Usha Kumari Salim Surani |
author_sort | Syeda Aasia Batool |
collection | DOAJ |
description | Mucormycosis is a rare but fatal disease caused by a filamentous fungus involving the nose, paranasal sinuses, and brain. These organisms usually cause severe infections in immunocompromised individuals. Granulomatous polyangiitis (GPA), also known as Wegner’s granulomatosis, is a rare, aseptic necrotizing granulomatous vasculitis involving small and medium-sized vessels commonly affecting the nose, ears, lungs, and kidneys. The simultaneous occurrence of mucormycosis and GPA, two rare diseases, in the same patient is exceedingly rare. In this case study, we describe a 40-year-old woman who presented with manifestations of both GPA and mucormycosis. She was started with steroids and antifungal agents and achieved significant improvement. |
format | Article |
id | doaj-art-7a30da41d9e2496aabaf647d5651333a |
institution | Kabale University |
issn | 2090-6633 |
language | English |
publishDate | 2023-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Infectious Diseases |
spelling | doaj-art-7a30da41d9e2496aabaf647d5651333a2025-02-03T05:44:20ZengWileyCase Reports in Infectious Diseases2090-66332023-01-01202310.1155/2023/7934700Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous PolyangiitisSyeda Aasia Batool0Usha Kumari1Salim Surani2Holy Family HospitalDow University of Health SciencesMedicine & PharmacologyMucormycosis is a rare but fatal disease caused by a filamentous fungus involving the nose, paranasal sinuses, and brain. These organisms usually cause severe infections in immunocompromised individuals. Granulomatous polyangiitis (GPA), also known as Wegner’s granulomatosis, is a rare, aseptic necrotizing granulomatous vasculitis involving small and medium-sized vessels commonly affecting the nose, ears, lungs, and kidneys. The simultaneous occurrence of mucormycosis and GPA, two rare diseases, in the same patient is exceedingly rare. In this case study, we describe a 40-year-old woman who presented with manifestations of both GPA and mucormycosis. She was started with steroids and antifungal agents and achieved significant improvement.http://dx.doi.org/10.1155/2023/7934700 |
spellingShingle | Syeda Aasia Batool Usha Kumari Salim Surani Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis Case Reports in Infectious Diseases |
title | Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis |
title_full | Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis |
title_fullStr | Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis |
title_full_unstemmed | Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis |
title_short | Two Rare Diseases, One Patient: A Case Report of Mucormycosis and Granulomatous Polyangiitis |
title_sort | two rare diseases one patient a case report of mucormycosis and granulomatous polyangiitis |
url | http://dx.doi.org/10.1155/2023/7934700 |
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