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Fatal disseminated mucormycosis associated with COVID‐19
Secondary fungal infections are a critical problem that accompany immunosuppressive therapy for severe coronavirus disease 2019 (COVID‐19). We report a fatal case of COVID‐19 with disseminated mucormycosis diagnosed during autopsy. A 58‐year‐old man with diabetes was hospitalized for severe COVID‐19...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841239/ https://www.ncbi.nlm.nih.gov/pubmed/35198214 http://dx.doi.org/10.1002/rcr2.912 |
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author | Horiguchi, Tomoya Tsukamoto, Tetsuya Toyama, Yoko Sasaki, Toshiharu Nakamura, Tomoyuki Sakurai, Aki Kuriyama, Naohide Komatsu, Satoshi Shigeyasu, Yoshiko Ina, Takuma Sakurai, Eiko Nakajima, Noriko Tsuchimori, Arisa Yamada, Seiji Suzuki, Tadaki Imaizumi, Kazuyoshi |
author_facet | Horiguchi, Tomoya Tsukamoto, Tetsuya Toyama, Yoko Sasaki, Toshiharu Nakamura, Tomoyuki Sakurai, Aki Kuriyama, Naohide Komatsu, Satoshi Shigeyasu, Yoshiko Ina, Takuma Sakurai, Eiko Nakajima, Noriko Tsuchimori, Arisa Yamada, Seiji Suzuki, Tadaki Imaizumi, Kazuyoshi |
author_sort | Horiguchi, Tomoya |
collection | PubMed |
description | Secondary fungal infections are a critical problem that accompany immunosuppressive therapy for severe coronavirus disease 2019 (COVID‐19). We report a fatal case of COVID‐19 with disseminated mucormycosis diagnosed during autopsy. A 58‐year‐old man with diabetes was hospitalized for severe COVID‐19 and treated with remdesivir, systemic steroids and tocilizumab. Following treatment, he was provided extracorporeal membrane oxygenation support. However, he died of multiple organ failure accompanied by pulmonary and kidney infarction, as revealed by computed tomography. Autopsy revealed that the infarction was caused by thromboangiitis due to mucormycosis in the brain, lungs, heart, liver and kidneys. Therefore, the diagnosis of disseminated mucormycosis was established. Disseminated mucormycosis is a rare complication of COVID‐19. Although its early diagnosis is difficult, the disease progresses rapidly. Hence, we propose that immunosuppressive treatment for COVID‐19 should be administered with caution considering the risk of developing severe opportunistic infections, such as mucormycosis. |
format | Online Article Text |
id | pubmed-8841239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88412392022-02-22 Fatal disseminated mucormycosis associated with COVID‐19 Horiguchi, Tomoya Tsukamoto, Tetsuya Toyama, Yoko Sasaki, Toshiharu Nakamura, Tomoyuki Sakurai, Aki Kuriyama, Naohide Komatsu, Satoshi Shigeyasu, Yoshiko Ina, Takuma Sakurai, Eiko Nakajima, Noriko Tsuchimori, Arisa Yamada, Seiji Suzuki, Tadaki Imaizumi, Kazuyoshi Respirol Case Rep Case Reports Secondary fungal infections are a critical problem that accompany immunosuppressive therapy for severe coronavirus disease 2019 (COVID‐19). We report a fatal case of COVID‐19 with disseminated mucormycosis diagnosed during autopsy. A 58‐year‐old man with diabetes was hospitalized for severe COVID‐19 and treated with remdesivir, systemic steroids and tocilizumab. Following treatment, he was provided extracorporeal membrane oxygenation support. However, he died of multiple organ failure accompanied by pulmonary and kidney infarction, as revealed by computed tomography. Autopsy revealed that the infarction was caused by thromboangiitis due to mucormycosis in the brain, lungs, heart, liver and kidneys. Therefore, the diagnosis of disseminated mucormycosis was established. Disseminated mucormycosis is a rare complication of COVID‐19. Although its early diagnosis is difficult, the disease progresses rapidly. Hence, we propose that immunosuppressive treatment for COVID‐19 should be administered with caution considering the risk of developing severe opportunistic infections, such as mucormycosis. John Wiley & Sons, Ltd 2022-02-13 /pmc/articles/PMC8841239/ /pubmed/35198214 http://dx.doi.org/10.1002/rcr2.912 Text en © 2022 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Horiguchi, Tomoya Tsukamoto, Tetsuya Toyama, Yoko Sasaki, Toshiharu Nakamura, Tomoyuki Sakurai, Aki Kuriyama, Naohide Komatsu, Satoshi Shigeyasu, Yoshiko Ina, Takuma Sakurai, Eiko Nakajima, Noriko Tsuchimori, Arisa Yamada, Seiji Suzuki, Tadaki Imaizumi, Kazuyoshi Fatal disseminated mucormycosis associated with COVID‐19 |
title | Fatal disseminated mucormycosis associated with COVID‐19 |
title_full | Fatal disseminated mucormycosis associated with COVID‐19 |
title_fullStr | Fatal disseminated mucormycosis associated with COVID‐19 |
title_full_unstemmed | Fatal disseminated mucormycosis associated with COVID‐19 |
title_short | Fatal disseminated mucormycosis associated with COVID‐19 |
title_sort | fatal disseminated mucormycosis associated with covid‐19 |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841239/ https://www.ncbi.nlm.nih.gov/pubmed/35198214 http://dx.doi.org/10.1002/rcr2.912 |
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