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ID 67615
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Author
Yamashita, Masahiro Department of Allergy and Respiratory Medicine, Okayama University Hospital
Higo, Hisao Department of Allergy and Respiratory Medicine, Okayama University Hospital
Fujii, Nobuharu Department of Hematology and Oncology, Okayama University Hospital Kaken ID publons researchmap
Matsumoto, Chiaki Department of Allergy and Respiratory Medicine, Okayama University Hospital
Makimoto, Go Department of Allergy and Respiratory Medicine, Okayama University Hospital
Ninomiya, Kiichiro Center for Comprehensive Genomic Medicine, Okayama University Hospital Kaken ID
Fujii, Masanori Department of Allergy and Respiratory Medicine, Okayama University Hospital
Rai, Kammei Center for Innovative Clinical Medicine, Okayama University Hospital
Ichihara, Eiki Center for Clinical Oncology, Okayama University Hospital Kaken ID publons
Ohashi, Kadoaki Department of Allergy and Respiratory Medicine, Okayama University Hospital ORCID Kaken ID researchmap
Hotta, Katsuyuki Center for Innovative Clinical Medicine, Okayama University Hospital Kaken ID publons researchmap
Tabata, Masahiro Center for Clinical Oncology, Okayama University Hospital Kaken ID researchmap
Maeda, Yoshinobu Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID researchmap
Miyahara, Nobuaki Department of Allergy and Respiratory Medicine, Okayama University Hospital Kaken ID publons researchmap
Abstract
A 56-year-old woman who received CD19 chimeric antigen receptor-T cell therapy for refractory diffuse large B-cell lymphoma developed severe coronavirus disease 2019 (COVID-19) and was treated with nirmatrelvir/ritonavir in April 2022. However, she experienced persistent fatigue and cough and fever in June. Computed tomography revealed bilateral ground-glass opacities (GGO), and the patient was treated with corticosteroids for organizing pneumonia after COVID19. Partial improvement was observed, but new GGO appeared despite corticosteroid therapy. Genome analysis of severe acute respiratory syndrome coronavirus 2 detected Omicron variant BA.1.1.2, which was prevalent at the time of initial infection. The patient was diagnosed with protracted COVID-19 and was treated with remdesivir, molnupiravir, nirmatrelvir/ritonavir, and tixagevimab/cilgavimab. These treatments appeared to contribute to the improvement of protracted COVID-19.
Keywords
Chimeric antigen receptor-T cell therapy
Coronavirus disease 2019
Multidrug therapy
Organizing pneumonia
Published Date
2024
Publication Title
Respiratory Medicine Case Reports
Volume
volume51
Publisher
Elsevier
Start Page
102104
ISSN
2213-0071
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2024 The Authors.
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publisher
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1016/j.rmcr.2024.102104
License
http://creativecommons.org/licenses/by-nc-nd/4.0/