Division of Medical Oncology/Hematology, Department of Medicine, Kobe University Graduate School of Medicine, Japan.
Department of Transfusion Medicine and Cell Therapy, Kobe University Hospital, Japan.
Intern Med. 2023 Jan 15;62(2):285-292. doi: 10.2169/internalmedicine.9711-22. Epub 2022 Jun 14.
A 68-year-old man was admitted because of a left shoulder mass and swollen right testis. Pathological examinations indicated a diagnosis of diffuse large B-cell lymphoma (DLBCL) with the CD20+BCL6+MUM1+BCL2+CD10-MYC- phenotype in both lesions. G-banding of soft tissue showed 47,XY,+18, whereas testicular cells showed 47,X,+X,-Y,der (4) t (4;18) (p15;?),del (5) (q?),+13. Fluorescence in situ hybridization detected additional MALT1 and BCL2 signals in both lesions. Southern blot demonstrated different IGH rearrangements between the soft tissue and testis. The patient was diagnosed with biclonal DLBCL with different karyotypes but similar immunophenotypes. Partial trisomy 18q involving MALT1 and BCL2 may be commonly involved in the pathogenesis of this biclonal DLBCL.
一位 68 岁男性因左肩部肿块和右侧睾丸肿胀而入院。病理检查提示弥漫性大 B 细胞淋巴瘤(DLBCL)的诊断,两个病变均表现为 CD20+BCL6+MUM1+BCL2+CD10-MYC-表型。软组织 G 带显示 47,XY,+18,而睾丸细胞显示 47,X,+X,-Y,der (4) t (4;18) (p15;?),del (5) (q?),+13。荧光原位杂交检测到两个病变中均存在额外的 MALT1 和 BCL2 信号。Southern 印迹显示软组织和睾丸之间存在不同的 IGH 重排。该患者被诊断为具有不同核型但相似免疫表型的双克隆 DLBCL。部分 18q 三体,涉及 MALT1 和 BCL2,可能共同参与这种双克隆 DLBCL 的发病机制。