Journal of Clinical and Experimental Hematopathology
Online ISSN : 1880-9952
Print ISSN : 1346-4280
ISSN-L : 1346-4280
Case report
MYD88 mutation-positive indolent B-cell lymphoma with CNS involvement: Bing–Neel syndrome mimickers
Kenichiro TakedaShoichiro OkazakiRintaro MinamiAkihumi IchikiYusuke YamagaKosei NakajimaKunio KitamuraKennosuke KarubeTakahiro Nishiyama
著者情報
ジャーナル オープンアクセス

2024 年 64 巻 3 号 p. 252-260

詳細
抄録

MYD88 p.L265P mutation occurs in over 90% of Waldenström’s macroglobulinemia (WM), which is characterized by lymphoplasmacytic lymphoma (LPL) with monoclonal IgM. WM requires careful diagnosis due to overlapping features with other B-cell malignancies. Bing–Neel syndrome (BNS), a rare complication of WM, involves central nervous system (CNS) invasion. This report describes two cases of morphologically low-grade B-cell lymphoma in the bone marrow accompanied by the presence of a large B-cell lymphoma in the brain and a common MYD88 p.L265P mutation, which were eventually established as BNS mimickers. Although the two components in these cases showed the same identical light-chain restriction, different immunoglobulin heavy-chain rearrangement peaks indicated distinct lymphoma stem cells for CNS and bone marrow lesions. These clinical cases emphasize the challenges in diagnosing BNS. Based on the findings, biopsy is recommended for accurate identification of the clonal relationship and MYD88 mutation status.

著者関連情報
© 2024 by The Japanese Society for Lymphoreticular Tissue Research

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
https://creativecommons.org/licenses/by-nc-sa/4.0/deed.ja
前の記事 次の記事
feedback
Top