淋巴瘤
长春新碱
美罗华
弥漫性大B细胞淋巴瘤
CD20
病理
人口
医学
BCL6公司
环磷酰胺
外周T细胞淋巴瘤
未另行规定
切碎
B细胞
化疗
T细胞
抗体
免疫学
生发中心
内科学
免疫系统
环境卫生
作者
Sho Yamazaki,Yosei Fujioka,Fumihiko Nakamura,Satoshi Ota,Aya Shinozaki‐Ushiku,Go Yamamoto,Yasuhiko Kamikubo,Yasuhito Nannya,Motoshi Ichikawa,Masashi Fukayama,Mineo Kurokawa
标识
DOI:10.1111/j.1440-1827.2011.02713.x
摘要
Composite lymphoma is defined as two or more distinct types of lymphoma in a single anatomical site. Among various combinations, composite B‐cell and T‐cell non‐Hodgkin's lymphomas (CBTL) are very infrequent. Herein we describe a 66‐year‐old female with CBTL presenting with lymphadenopathy, multiple bone lesions and an epidural tumor. Light microscopic examination of a biopsied cervical node revealed a dual population of lymphoid cells: sheets of large cells admixed with medium‐sized cells. The large cells expressed B‐cell markers and showed immunoglobulin light chain restriction, consistent with diffuse large B‐cell lymphoma (DLBCL). The medium‐sized cells were positive for CD20 as well as T‐cell markers. Because polymerase chain reaction amplification showed monoclonal rearrangement of the T‐cell receptor β chain gene, this population was compatible with peripheral T‐cell lymphoma not otherwise specified (PTCL‐NOS). We therefore made a diagnosis of composite DLBCL and CD20‐positive PTCL‐NOS. Complete remission was achieved after six cycles of R‐CHOP regimen (rituximab, doxorubicin, vincristine, cyclophosphamide and prednisolone). This is the first report of CD20‐positive PTCL‐NOS associated with composite lymphoma. Moreover, a literature review of composite DLBCL and PTCL‐NOS indicates that this rare clinical entity may be featured by efficacy of systemic chemotherapy in spite of prevalent extranodal lesions.
科研通智能强力驱动
Strongly Powered by AbleSci AI