| ID | 69580 |
| FullText URL | |
| Author |
Ikeda, Daisuke
Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Nawada, Tomohiro
The Center for Graduate Medical Education, Okayama University Hospital
Kondo, Takumi
Department of Hematology and Oncology, Okayama University Hospital
Shinohara, Takayuki
Department of Fungal Infection, National Institute of Infectious Diseases
Nagano, Tomohiro
Department of Hematology and Oncology, Okayama University Hospital
Kubota, Saya
Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Hiyama, Ryuichiro
Department of Hematology and Oncology, Okayama University Hospital
Ueno, Masaya
Department of Hematology and Oncology, Okayama University Hospital
Kobayashi, Hiroki
Department of Hematology and Oncology, Okayama University Hospital
Seike, Keisuke
Department of Hematology and Oncology, Okayama University Hospital
Fujiwara, Hideaki
Department of Hematology and Oncology, Okayama University Hospital
Asada, Noboru
Department of Hematology and Oncology, Okayama University Hospital
Kaken ID
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Ennishi, Daisuke
Department of Hematology and Oncology, Okayama University Hospital
Fujii, Keiko
Department of Hematology and Oncology, Okayama University Hospital
Kaken ID
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Fujii, Nobuharu
Department of Hematology and Oncology, Okayama University Hospital
Kaken ID
publons
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Makita, Masanori
Department of Hematology, Chugoku Central Hospital
Maeda, Yoshinobu
Department of Hematology and Oncology, Okayama University Hospital
Kaken ID
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| Abstract | Introduction: Invasive fungal infection (IFI) after chimeric antigen receptor (CAR) T-cell therapy is less common than bacterial and viral infections, but can be fatal once it develops. As most cases occur within 30 days after CAR T-cell infusion, late-onset IFI—particularly mould infection—appears to be under-recognised.
Discussion: We report an illustrative case of pituitary aspergillosis developing as late as one year after CD19 CAR T-cell therapy, highlighting a persistent risk in certain patients with delayed immune reconstitution. Conclusion: This case underscores the need for continued vigilance and individualised antifungal strategies to prevent IFI beyond the early post-infusion period. Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission. |
| Keywords | aspergillosis
CD19 CAR T
invasive fungal infection
pituitary
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| Published Date | 2025-09-02
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| Publication Title |
eJHaem
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| Volume | volume6
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| Issue | issue5
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| Publisher | Wiley
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| Start Page | e70138
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| ISSN | 2688-6146
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| Content Type |
Journal Article
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| language |
English
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| OAI-PMH Set |
岡山大学
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| Copyright Holders | © 2025 The Author(s).
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| File Version | publisher
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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| Related Url | isVersionOf https://doi.org/10.1002/jha2.70138
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| License | http://creativecommons.org/licenses/by/4.0/
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| Citation | D. Ikeda, T. Nawada, T. Kondo, et al. “ Late-Onset Invasive Aspergillosis With Pituitary Involvement and Dysfunction Following CD19 Chimeric Antigen Receptor T-Cell Therapy.” eJHaem 6, no. 5 (2025): 6, e70138. https://doi.org/10.1002/jha2.70138
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