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血管免疫母细胞性T细胞淋巴瘤1例
引用本文:张莹,刘焕强.血管免疫母细胞性T细胞淋巴瘤1例[J].中国麻风皮肤病杂志,2018,34(6):345-346.
作者姓名:张莹  刘焕强
作者单位:1河北医科大学研究生学院 河北 石家庄 050017 2河北省中医院 河北 石家庄 050011
摘    要:患者,男,64岁,躯干部丘疹1个月,皮疹逐渐增多,瘙痒明显,淋巴结肿大伴高热。淋巴结病理检查可见病理性核分裂象。免疫组化示:Ki-67标记指数约90%、CD21及CD23(示FDC网结构紊乱)、CD3及CD5(+)、CD34(血管+)、CD30(免疫母细胞+)、BCL-2(+)。 诊断:血管免疫母细胞性T细胞淋巴瘤。

关 键 词:剧烈瘙痒  血管免疫母细胞性T细胞淋巴瘤  

Angioimmunoblastic T-cell lymphoma: a case report
ZHANG Ying,LIU Huanqiang.Angioimmunoblastic T-cell lymphoma: a case report[J].China Journal of Leprosy and Skin Diseases,2018,34(6):345-346.
Authors:ZHANG Ying  LIU Huanqiang
Institution:1.Graduate School of the Hebei Medical University, Shijiazhuang 050017, Hebei ; 2.Hebei Provincial Hospital of traditional Chinese medicine, Shijiazhuang 050011 , Hebei
Abstract:A 64-years-old male presented with papule, no severe itching for 1 month. The disease gradually aggravated including papule?increasing, lymphadenectasis and fever. Biopsy?of?lymph node showed irregular mitosisis. Immunohistochemistry showed positive for CD21, CD23, CD3, CD5, CD34, CD30, BCL-2. Ki-67 Ki67 was positive in about 90% of the cells. The diagnosis of angioimmunoblastic T-cell lymphoma was made.
Keywords:atypical rash  severe itching  angioimmunoblastic T-cell lymphoma  
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