Terao Toshiki, Sato Yumiko, Kuroda Yoshiaki, Haratake Tomoka, Nishimura Midori Filiz, Sato Yasuharu, Kuyama Shoichi
Department of Hematology, NHO Iwakuni Clinical Center, Iwakuni, Japan.
Department of Hematology, Oncology, and Respiratory Medicine, Okayama University Medical School, Okayama, Japan.
J Clin Exp Hematop. 2024 Dec 25;64(4):318-322. doi: 10.3960/jslrt.24050. Epub 2024 Nov 28.
A 79-year-old Japanese woman presented with exertional dyspnea. She had cardiac tamponade and urgent pericardial drainage was performed. Pathological findings from the pericardial fluid revealed non-germinal center B-cell (non-GCB) pericardial large B-cell lymphoma (CD10, BCL6, and MUM1). Although a diagnosis of fluid overload-associated large B-cell lymphoma was considered, GCB nodal diffuse large B-cell lymphoma (CD10, BCL6, and MUM1) was discovered through needle biopsy of the enlarged left axillary lymph node. Despite the two lymphomas exhibiting different expression levels of CD10, polymerase chain reaction assessing IgH gene rearrangement suggested a clonal relationship between them. Additionally, MYD88 L265P mutation was confirmed using Sanger sequencing in both samples, suggesting the MCD type. Our case highlights a discrepancy between the Hans' criteria and the gene expression profile-based cell of origin.
一名79岁的日本女性因劳力性呼吸困难就诊。她患有心脏压塞,遂进行了紧急心包引流。心包积液的病理检查结果显示为非生发中心B细胞(non-GCB)心包大B细胞淋巴瘤(CD10、BCL6和MUM1)。尽管考虑诊断为液体超负荷相关的大B细胞淋巴瘤,但通过对肿大的左腋窝淋巴结进行针吸活检发现是生发中心B细胞(GCB)结内弥漫性大B细胞淋巴瘤(CD10、BCL6和MUM1)。尽管这两种淋巴瘤的CD10表达水平不同,但评估IgH基因重排的聚合酶链反应表明它们之间存在克隆关系。此外,在两个样本中使用桑格测序均证实了MYD88 L265P突变,提示为MCD型。我们的病例突出了汉斯标准与基于基因表达谱的细胞起源之间的差异。