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Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy
INTRODUCTION: Endobronchial mucormycosis is very rare with only few cases reported in the literature. Here, we report a rare presentation of pulmonary mucormycosis in a diabetic patient who presented with left lung collapse. Bronchoscopy revealed an endobronchial growth, mimicking a tumor, causing c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205427/ https://www.ncbi.nlm.nih.gov/pubmed/37229281 http://dx.doi.org/10.1016/j.idcr.2023.e01781 |
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author | Assal, Hebatallah Hany Hussein, Sabah Ahmed Mostafa, Ahmed El-Kareem, Dalia Abd Alfishawy, Mostafa Salah, Maged Mohammed, Habiballah Galal |
author_facet | Assal, Hebatallah Hany Hussein, Sabah Ahmed Mostafa, Ahmed El-Kareem, Dalia Abd Alfishawy, Mostafa Salah, Maged Mohammed, Habiballah Galal |
author_sort | Assal, Hebatallah Hany |
collection | PubMed |
description | INTRODUCTION: Endobronchial mucormycosis is very rare with only few cases reported in the literature. Here, we report a rare presentation of pulmonary mucormycosis in a diabetic patient who presented with left lung collapse. Bronchoscopy revealed an endobronchial growth, mimicking a tumor, causing complete occlusion of the left main bronchus. Histopathology confirmed the diagnosis of invasive mucormycosis. CASE PRESENTATION: Male patient 35 years old with accidental discovered Diabetes Mellitus, complained of hoarseness of voice and dry irritating cough that didn’t respond to antitussives and nonspecific treatment. CT chest was done and revealed left total lung collapse. Fiberoptic bronchoscopy was done and revealed total occlusion of the left main bronchus with whitish fungating glistening tissue from which biopsies were obtained. Histopathological examination was consistent with mucormycosis. A trial of medical treatment failed after which the patient was referred for surgical resection. CONCLUSION: Successful treatment of mucormycosis requires early diagnosis; prompt administration of antifungal therapy, and surgical intervention when applicable. Aggressive surgical intervention to remove necrotic tissue is generally accepted as the therapeutic mainstay for endobronchial obstructing mucormycosis |
format | Online Article Text |
id | pubmed-10205427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102054272023-05-24 Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy Assal, Hebatallah Hany Hussein, Sabah Ahmed Mostafa, Ahmed El-Kareem, Dalia Abd Alfishawy, Mostafa Salah, Maged Mohammed, Habiballah Galal IDCases Case Report INTRODUCTION: Endobronchial mucormycosis is very rare with only few cases reported in the literature. Here, we report a rare presentation of pulmonary mucormycosis in a diabetic patient who presented with left lung collapse. Bronchoscopy revealed an endobronchial growth, mimicking a tumor, causing complete occlusion of the left main bronchus. Histopathology confirmed the diagnosis of invasive mucormycosis. CASE PRESENTATION: Male patient 35 years old with accidental discovered Diabetes Mellitus, complained of hoarseness of voice and dry irritating cough that didn’t respond to antitussives and nonspecific treatment. CT chest was done and revealed left total lung collapse. Fiberoptic bronchoscopy was done and revealed total occlusion of the left main bronchus with whitish fungating glistening tissue from which biopsies were obtained. Histopathological examination was consistent with mucormycosis. A trial of medical treatment failed after which the patient was referred for surgical resection. CONCLUSION: Successful treatment of mucormycosis requires early diagnosis; prompt administration of antifungal therapy, and surgical intervention when applicable. Aggressive surgical intervention to remove necrotic tissue is generally accepted as the therapeutic mainstay for endobronchial obstructing mucormycosis Elsevier 2023-05-12 /pmc/articles/PMC10205427/ /pubmed/37229281 http://dx.doi.org/10.1016/j.idcr.2023.e01781 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Assal, Hebatallah Hany Hussein, Sabah Ahmed Mostafa, Ahmed El-Kareem, Dalia Abd Alfishawy, Mostafa Salah, Maged Mohammed, Habiballah Galal Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
title | Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
title_full | Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
title_fullStr | Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
title_full_unstemmed | Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
title_short | Endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
title_sort | endobronchial mucormycosis diagnosed by fiberoptic bronchoscopy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205427/ https://www.ncbi.nlm.nih.gov/pubmed/37229281 http://dx.doi.org/10.1016/j.idcr.2023.e01781 |
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