中国麻风皮肤病杂志 ›› 2018, Vol. 34 ›› Issue (6): 345-346.

• 短篇论著 • 上一篇    下一篇

血管免疫母细胞性T细胞淋巴瘤1例

张 莹1，刘焕强1,2   

  1. 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
  • 出版日期:2018-06-15 发布日期:2018-12-11
  • 通讯作者: 刘焕强，E-mail：liuhuanqiang@sina.com

Angioimmunoblastic T-cell lymphoma: a case report

ZHANG Ying1 , LIU Huanqiang1,2   

  1. 1.Graduate School of the Hebei Medical University, Shijiazhuang 050017, Hebei ; 2.Hebei Provincial Hospital of traditional Chinese medicine, Shijiazhuang 050011 , Hebei
  • Online:2018-06-15 Published:2018-12-11
  • Contact: E-mail: liuhuanqiang@sina.com

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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

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.

Key words: atypical rash, severe itching, angioimmunoblastic T-cell lymphoma