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Title: Insulin-like growth factor II mRNA binding protein 3 is highly expressed in primary diffuse large B-cell lymphoma of the CNS
Authors: Odani, Kentaro
Fujimoto, Masakazu  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0575-6507 (unconfirmed)
Fujii, Hirotake
Saka, Manduwa
Mizoguchi, Kai
Hirata, Masahiro
Sakurai, Takaki
Takeuchi, Yasuhide
Minamiguchi, Sachiko
Arakawa, Yoshiki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-4626-4645 (unconfirmed)
Haga, Hironori  kyouindb  KAKEN_id
Author's alias: 藤本, 正数
溝口, 佳惟
平田, 勝啓
竹内, 康英
南口, 早智子
荒川, 芳輝
羽賀, 博典
Keywords: primary diffuse large B-cell lymphoma of the central nervous system
insulin-like growth factor II mRNA binding protein 3
immunohistochemistry
Issue Date: 2024
Publisher: Japanese Society for Lymphoreticular Tissue Research
Journal title: Journal of Clinical and Experimental Hematopathology
Volume: 64
Issue: 3
Start page: 203
End page: 207
Abstract: Primary diffuse large B-cell lymphoma of the central nervous system (CNS-DLBCL) can be difficult to diagnose because of the limited amount of biopsy tissue. Here, we analyzed the utility of insulin-like growth factor II mRNA binding protein 3 (IMP3) immunohistochemistry (IHC) as an adjunctive diagnostic tool for CNS-DLBCL. IHC was performed on 57 biopsy samples (55 brain biopsy samples and two vitreous cell blocks) from 54 patients with CNS-DLBCL, including three biopsy samples initially diagnosed as negative or indeterminate for CNS-DLBCL. Additionally, IMP3 IHC was performed on 68 DLBCLs other than CNS-DLBCL and 12 inflammatory brain diseases. Cytoplasmic IMP3 expression was noted in ≥ 50% of tumor cells in 100% (57/57) of CNS-DLBCLs and 88.2% (60/68) of non-CNS-DLBCLs. In contrast, no IMP3-positive CD20-positive B cells were observed in the inflammatory brain disease (P < 0.0001). In conclusion, IMP3 is highly expressed in CNS-DLBCL. However, it is also expressed in other types of DLBCLs, making it less specific. Most CNS-DLBCL cases can be diagnosed without performing IHC for IMP3 expression, but it may be a useful adjunctive tool to differentiate from reactive lesions when tumor cells are few or deformed.
Rights: © 2024 The Japanese Society for Lymphoreticular Tissue Research
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
URI: http://hdl.handle.net/2433/290118
DOI(Published Version): 10.3960/jslrt.24025
PubMed ID: 39343609
Appears in Collections:Journal Articles

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