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An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report

BACKGROUND: Recently, deaths due to mucormycosis in immunocompromised hosts have increased; however, the clinical and pathological features of mucormycosis are not fully understood, especially in view of the associated high mortality and rare incidence in immunocompetent patients. CASE PRESENTATION:...

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Autores principales: Harada, Masanori, Yasuda, Kazuyo, Uruchida, Kazumi, Yamashita, Ryoma, Morikawa, Keisuke, Ito, Yutaro, Mochizuki, Eisuke, Matsuura, Shun, Tsukui, Masaru, Koshimizu, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022292/
https://www.ncbi.nlm.nih.gov/pubmed/36932380
http://dx.doi.org/10.1186/s12890-023-02382-y
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author Harada, Masanori
Yasuda, Kazuyo
Uruchida, Kazumi
Yamashita, Ryoma
Morikawa, Keisuke
Ito, Yutaro
Mochizuki, Eisuke
Matsuura, Shun
Tsukui, Masaru
Koshimizu, Naoki
author_facet Harada, Masanori
Yasuda, Kazuyo
Uruchida, Kazumi
Yamashita, Ryoma
Morikawa, Keisuke
Ito, Yutaro
Mochizuki, Eisuke
Matsuura, Shun
Tsukui, Masaru
Koshimizu, Naoki
author_sort Harada, Masanori
collection PubMed
description BACKGROUND: Recently, deaths due to mucormycosis in immunocompromised hosts have increased; however, the clinical and pathological features of mucormycosis are not fully understood, especially in view of the associated high mortality and rare incidence in immunocompetent patients. CASE PRESENTATION: We have described a rare autopsy case of a 67-year-old Japanese man with chronic obstructive pulmonary disease who contracted mucormycosis. He had not been on any immunosuppressants, and his immune functions were intact. Since 3 days prior to admission to our hospital, he had experienced progressive dyspnea, productive cough, and fever. Chest computed tomography revealed pleural effusion in the left lower hemithorax and consolidation in the right lung field. Although he was administered with tazobactam-piperacillin hydrate (13.5 g/day), renal dysfunction occurred on the ninth disease day. Therefore, it was switched to cefepime (2 g/day). However, his general condition and lung-field abnormality worsened gradually. Cytological analysis of the sputum sample at admission mainly revealed sporangiophores and unicellular sporangioles, while repeated sputum culture yielded Cunninghamella species. Therefore, he was diagnosed with pulmonary mucormycosis. Liposomal amphotericin B (5 mg/kg/day) was initiated on the 28(th) disease day. However, chest radiography and electrocardiography detected cardiomegaly and atrial fibrillation, respectively, and he died on the 37(th) disease day. A postmortem examination revealed clusters of fungal hyphae within the arteries of the right pulmonary cavity wall, the subpericardial artery, intramyocardial capillary blood vessels, and the esophageal subserosa vein. Direct sequencing revealed that all fungal culture samples were positive for Cunninghamella bertholletiae. CONCLUSIONS: Cunninghamella bertholletiae could rapidly progress from colonizing the bronchi to infecting the surrounding organs via vascular invasion even in immunocompetent patients.
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spelling pubmed-100222922023-03-18 An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report Harada, Masanori Yasuda, Kazuyo Uruchida, Kazumi Yamashita, Ryoma Morikawa, Keisuke Ito, Yutaro Mochizuki, Eisuke Matsuura, Shun Tsukui, Masaru Koshimizu, Naoki BMC Pulm Med Case Report BACKGROUND: Recently, deaths due to mucormycosis in immunocompromised hosts have increased; however, the clinical and pathological features of mucormycosis are not fully understood, especially in view of the associated high mortality and rare incidence in immunocompetent patients. CASE PRESENTATION: We have described a rare autopsy case of a 67-year-old Japanese man with chronic obstructive pulmonary disease who contracted mucormycosis. He had not been on any immunosuppressants, and his immune functions were intact. Since 3 days prior to admission to our hospital, he had experienced progressive dyspnea, productive cough, and fever. Chest computed tomography revealed pleural effusion in the left lower hemithorax and consolidation in the right lung field. Although he was administered with tazobactam-piperacillin hydrate (13.5 g/day), renal dysfunction occurred on the ninth disease day. Therefore, it was switched to cefepime (2 g/day). However, his general condition and lung-field abnormality worsened gradually. Cytological analysis of the sputum sample at admission mainly revealed sporangiophores and unicellular sporangioles, while repeated sputum culture yielded Cunninghamella species. Therefore, he was diagnosed with pulmonary mucormycosis. Liposomal amphotericin B (5 mg/kg/day) was initiated on the 28(th) disease day. However, chest radiography and electrocardiography detected cardiomegaly and atrial fibrillation, respectively, and he died on the 37(th) disease day. A postmortem examination revealed clusters of fungal hyphae within the arteries of the right pulmonary cavity wall, the subpericardial artery, intramyocardial capillary blood vessels, and the esophageal subserosa vein. Direct sequencing revealed that all fungal culture samples were positive for Cunninghamella bertholletiae. CONCLUSIONS: Cunninghamella bertholletiae could rapidly progress from colonizing the bronchi to infecting the surrounding organs via vascular invasion even in immunocompetent patients. BioMed Central 2023-03-17 /pmc/articles/PMC10022292/ /pubmed/36932380 http://dx.doi.org/10.1186/s12890-023-02382-y Text en © The Author(s) 2023 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
Harada, Masanori
Yasuda, Kazuyo
Uruchida, Kazumi
Yamashita, Ryoma
Morikawa, Keisuke
Ito, Yutaro
Mochizuki, Eisuke
Matsuura, Shun
Tsukui, Masaru
Koshimizu, Naoki
An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report
title An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report
title_full An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report
title_fullStr An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report
title_full_unstemmed An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report
title_short An autopsy case of disseminated Cunninghamella bertholletiae infection in an immunocompetent patient: a case report
title_sort autopsy case of disseminated cunninghamella bertholletiae infection in an immunocompetent patient: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022292/
https://www.ncbi.nlm.nih.gov/pubmed/36932380
http://dx.doi.org/10.1186/s12890-023-02382-y
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