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Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature
BACKGROUND: Pulmonary mucormycosis caused by Mucorales is a highly lethal invasive fungal infection usually found in immunocompromised patients. Isolated pulmonary mucormycosis in immunocompetent patients is very rare. Here, we present a case of a 32-year-old male who developed pulmonary mucormycosi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077830/ https://www.ncbi.nlm.nih.gov/pubmed/33906622 http://dx.doi.org/10.1186/s12890-021-01504-8 |
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author | He, Jianhan Sheng, Gaohong Yue, Huihui Zhang, Fengqin Zhang, Hui-Lan |
author_facet | He, Jianhan Sheng, Gaohong Yue, Huihui Zhang, Fengqin Zhang, Hui-Lan |
author_sort | He, Jianhan |
collection | PubMed |
description | BACKGROUND: Pulmonary mucormycosis caused by Mucorales is a highly lethal invasive fungal infection usually found in immunocompromised patients. Isolated pulmonary mucormycosis in immunocompetent patients is very rare. Here, we present a case of a 32-year-old male who developed pulmonary mucormycosis without any known immunodeficiency. CASE PRESENTATION: The patient presented to our hospital because of cough and chest pain along with blood in the sputum. He was first treated for community-acquired pneumonia until bronchoalveolar lavage fluid culture confirmed the growth of Absidia. His symptoms were relieved with the use of amphotericin B, and he eventually recovered. We also provide a systematic review of relevant literature to summarize the characteristics of pulmonary mucormycosis in immunocompetent patients. CONCLUSIONS: Pulmonary mucormycosis has variable clinical presentations and is difficult to identify. Due to its high fatality rate, clinicians should make judgements regarding suspected cases correctly and in a timely manner to avoid misdiagnosis and delayed treatment. |
format | Online Article Text |
id | pubmed-8077830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80778302021-04-29 Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature He, Jianhan Sheng, Gaohong Yue, Huihui Zhang, Fengqin Zhang, Hui-Lan BMC Pulm Med Case Report BACKGROUND: Pulmonary mucormycosis caused by Mucorales is a highly lethal invasive fungal infection usually found in immunocompromised patients. Isolated pulmonary mucormycosis in immunocompetent patients is very rare. Here, we present a case of a 32-year-old male who developed pulmonary mucormycosis without any known immunodeficiency. CASE PRESENTATION: The patient presented to our hospital because of cough and chest pain along with blood in the sputum. He was first treated for community-acquired pneumonia until bronchoalveolar lavage fluid culture confirmed the growth of Absidia. His symptoms were relieved with the use of amphotericin B, and he eventually recovered. We also provide a systematic review of relevant literature to summarize the characteristics of pulmonary mucormycosis in immunocompetent patients. CONCLUSIONS: Pulmonary mucormycosis has variable clinical presentations and is difficult to identify. Due to its high fatality rate, clinicians should make judgements regarding suspected cases correctly and in a timely manner to avoid misdiagnosis and delayed treatment. BioMed Central 2021-04-27 /pmc/articles/PMC8077830/ /pubmed/33906622 http://dx.doi.org/10.1186/s12890-021-01504-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report He, Jianhan Sheng, Gaohong Yue, Huihui Zhang, Fengqin Zhang, Hui-Lan Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
title | Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
title_full | Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
title_fullStr | Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
title_full_unstemmed | Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
title_short | Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
title_sort | isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077830/ https://www.ncbi.nlm.nih.gov/pubmed/33906622 http://dx.doi.org/10.1186/s12890-021-01504-8 |
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