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Pancreatic T/histiocyte-rich large B-cell lymphoma: A case report and review of literature 被引量:7
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作者 Shu-Mei Zheng De-Jiang Zhou +7 位作者 Yi-Hua Chen Rui Jiang Yun-Xia Wang Yong Zhang Hong-Li Xue Hai-Qiong Wang Dong Mou Wei-Zheng Zeng 《World Journal of Gastroenterology》 SCIE CAS 2017年第24期4467-4472,共6页
Primary pancreatic lymphoma(PPL)is an extremely rare form of extranodal malignant lymphoma.The most common histological subtype of PPL is diffuse large B cell lymphoma(DLBCL).In rare cases,PPL can also present as foll... Primary pancreatic lymphoma(PPL)is an extremely rare form of extranodal malignant lymphoma.The most common histological subtype of PPL is diffuse large B cell lymphoma(DLBCL).In rare cases,PPL can also present as follicular lymphoma,small lymphocytic lymphoma,and T cell lymphoma either of non-Hodgkin’s lymphoma or of Hodgkin’s lymphoma.T-cell/histiocyterich large B-cell lymphoma(T/HRBCL)is an uncommon morphologic variant of DLBCL with aggressive clinical course,it is predominantly a nodal disease,but extranodal sites such as bone marrow,liver,and spleen can be involved.Pancreatic involvement of T/HRBCL was not presented before.Herein,we report a 48-year-old male who was hospitalized with complaints of jaundice,dark brown urine,pale stools,and nausea.The radiological evaluation revealed a pancreatic head mass and,following operative biopsy,the tumor was diagnosed as T/HRBCL.The patient achieved remission after six cycles of CHOP chemotherapy.Therefore,T/HRBCL can be treated similarly to the stage-matched DLBCL and both of them get equivalent outcomes after chemotherapy. 展开更多
关键词 Non-Hodgkins 淋巴 T-cell/histiocyte-rich B 房间淋巴 IMMUNOHISTOCHEMISTRY 主要胰腺的淋巴瘤 诊断
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