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A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report

Cytomegalovirus (CMV) infection is one of the most common infectious complications following hematopoietic stem cell transplantation (HSCT); however, cases involving multiple organs at the same time are rare. The present study describes a case of CMV pneumonia combined with CMV DNAemia and CMV cysti...

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Autores principales: Li, Qiqi, Liang, Quan, Meng, Rongmei, Xie, Qingqiao, Zhang, Yingzhen, Wei, Changjin, Wei, Yunjie, He, Kaiye, Li, Meihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443026/
https://www.ncbi.nlm.nih.gov/pubmed/37614422
http://dx.doi.org/10.3892/etm.2023.12153
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author Li, Qiqi
Liang, Quan
Meng, Rongmei
Xie, Qingqiao
Zhang, Yingzhen
Wei, Changjin
Wei, Yunjie
He, Kaiye
Li, Meihua
author_facet Li, Qiqi
Liang, Quan
Meng, Rongmei
Xie, Qingqiao
Zhang, Yingzhen
Wei, Changjin
Wei, Yunjie
He, Kaiye
Li, Meihua
author_sort Li, Qiqi
collection PubMed
description Cytomegalovirus (CMV) infection is one of the most common infectious complications following hematopoietic stem cell transplantation (HSCT); however, cases involving multiple organs at the same time are rare. The present study describes a case of CMV pneumonia combined with CMV DNAemia and CMV cystitis after HSCT. A 33-year-old male patient with acute myeloid leukemia was treated with HSCT. The first month after HSCT, the patient developed a cough and shortness of breath. At 2 months post-HSCT, the patient developed hematuria. The CMV DNA levels in the blood and urine were elevated; bronchoalveolar lavage fluid (BALF) was also positive for CMV DNA. Heterotypic cells exhibiting a large nuclear morphology were observed in the BALF and bronchial brushes. Recurrent and progressive ground-glass opacities were evident on chest computed tomography. The patient was diagnosed with CMV pneumonia complicated by CMV DNAemia and CMV cystitis, and was treated with a combination of ganciclovir and foscarnet, along with immunoglobulin therapy. The patient was cured and discharged. It was determined that the CMV DNA in the blood was inconsistent with that in the BALF, which delayed the early diagnosis of CMV pneumonia. The association between T-cell immune function and the therapeutic efficacy for CMV multi-organ infection following HSCT is known to be significant. Moreover, the timely administration of ganciclovir and foscarnet in combination with immunoglobulin therapy demonstrated favorable clinical outcomes.
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spelling pubmed-104430262023-08-23 A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report Li, Qiqi Liang, Quan Meng, Rongmei Xie, Qingqiao Zhang, Yingzhen Wei, Changjin Wei, Yunjie He, Kaiye Li, Meihua Exp Ther Med Case Report Cytomegalovirus (CMV) infection is one of the most common infectious complications following hematopoietic stem cell transplantation (HSCT); however, cases involving multiple organs at the same time are rare. The present study describes a case of CMV pneumonia combined with CMV DNAemia and CMV cystitis after HSCT. A 33-year-old male patient with acute myeloid leukemia was treated with HSCT. The first month after HSCT, the patient developed a cough and shortness of breath. At 2 months post-HSCT, the patient developed hematuria. The CMV DNA levels in the blood and urine were elevated; bronchoalveolar lavage fluid (BALF) was also positive for CMV DNA. Heterotypic cells exhibiting a large nuclear morphology were observed in the BALF and bronchial brushes. Recurrent and progressive ground-glass opacities were evident on chest computed tomography. The patient was diagnosed with CMV pneumonia complicated by CMV DNAemia and CMV cystitis, and was treated with a combination of ganciclovir and foscarnet, along with immunoglobulin therapy. The patient was cured and discharged. It was determined that the CMV DNA in the blood was inconsistent with that in the BALF, which delayed the early diagnosis of CMV pneumonia. The association between T-cell immune function and the therapeutic efficacy for CMV multi-organ infection following HSCT is known to be significant. Moreover, the timely administration of ganciclovir and foscarnet in combination with immunoglobulin therapy demonstrated favorable clinical outcomes. D.A. Spandidos 2023-08-04 /pmc/articles/PMC10443026/ /pubmed/37614422 http://dx.doi.org/10.3892/etm.2023.12153 Text en Copyright: © Li et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Report
Li, Qiqi
Liang, Quan
Meng, Rongmei
Xie, Qingqiao
Zhang, Yingzhen
Wei, Changjin
Wei, Yunjie
He, Kaiye
Li, Meihua
A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report
title A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report
title_full A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report
title_fullStr A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report
title_full_unstemmed A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report
title_short A successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: A case report
title_sort successfully cured case of cytomegalovirus multiple organ infection after hematopoietic stem cell transplantation: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443026/
https://www.ncbi.nlm.nih.gov/pubmed/37614422
http://dx.doi.org/10.3892/etm.2023.12153
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