摘要
按ＷＦ分类，弥漫型淋巴瘤２８例（８２．４％），滤胞型淋巴瘤６例（１７．６％）。免疫组化染色证明，Ｂ细胞性淋巴瘤３２例（９４．１％），Ｔ细胞性淋巴瘤２例（５．９％），其中１例原发于胃，ＵＣＨＬ、ＭＴＩ、ＣＤ３阳性，为多形细胞性淋巴瘤，另１例原发于小肠，ＵＣＨＬ１、ＣＤ３阳性，为混合细胞性淋巴瘤。组织学观察，滤胞中心细胞来源者最多见，其中弥漫型大细胞性淋巴瘤发病率最高（１８例，５２．９％），无裂细胞性淋巴瘤占４４．１％。
According to WF
classification, 28 cases(82. 4%)were of the diffuse type andthe other 6 cases (17.6%)the
follicular type。 Immunohistochemical studies revealed that 32cas-es(94. 1%)originated from B
cell, and 2 cases(5.9%)T cell, of which one case was of theIBL polymorphous type developed in
the stomach and the other one the diffuse mixed type devel-oped in the small intestine。
Histologically, diffuse large cell lymphoma was the most preponder-anttype,being as high as
18 cases (52·9%), of which diffuse large non-cleaved was the high-esr
出处
《白求恩医科大学学报》
CSCD
1994年第3期224-226,共3页
Journal of Norman Bethune University of Medical Science
关键词
淋巴瘤
病理
肠肿瘤
免疫组织化学
immunohistochemistry
lymphoma/PA
lymphomal/CL
gastrointestinal neo- plams/PA School
of medical sciences, Akita University,Japan
