摘要
目的:探讨罕见的复合性淋巴瘤的临床病理特征。方法:采用形态学、免疫组织化学及分子遗传学方法对1例颈部复合性的黏膜相关淋巴组织淋巴瘤及外周T细胞淋巴瘤进行临床病理分析并复习文献。结果:本例复合性B与T细胞淋巴瘤在形态上有黏膜相关淋巴组织淋巴瘤和外周T细胞淋巴瘤的特征,且IgH和TCR基因重排。结论:复合性淋巴瘤罕见,诊断需结合形态、免疫表型和分子遗传学特征。
Objective：To report and discuss the clinicopathological features of a rare composite lymphoma on neck.Method：A case of composite MALT lymphoma and peripheral T cell lymphoma was studied by histopathology,immunohistochemistry and molecular genetics with review of literatures.Result：This case of composite B and T cell lymphoma had MALT lymphoma in one lymphoma node and unspecified peripheral T-cell lymphoma in another,which expressed CD20 and CD3 separately.IgH and TCR gene rearrangements were also detected.Conclusion：Composite lymphoma is a rare tumor.The diagnosis of composite lymphoma should be made with combination of morphology,immunophenotype and molecular genetics to avoid misdiagnosis.
出处
《临床血液学杂志》
CAS
2011年第2期148-150,共3页
Journal of Clinical Hematology
作者简介
现在中国人民解放军海军总医院工作
通信作者：侯健，E-mail：houjian167@sohu．com
