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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Main Authors: Syeda Aasia Batool, Usha Kumari, Salim Surani
Format: Article
Language:English
Published: Wiley 2023-01-01
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.
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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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