中国麻风皮肤病杂志 ›› 2020, Vol. 36 ›› Issue (9): 546-547.doi: 10.12144/zgmfskin202009546

• 病例报告 • 上一篇    下一篇

局限型淋巴瘤样丘疹病一例

董玲玲1,张玮琨1,孔祥君2,聂振华2   

  1. 1天津中医药大学，天津，300193；2天津中医药研究院附属医院皮肤科，天津，300120
  • 出版日期:2020-09-15 发布日期:2020-08-21
  • 通讯作者: 聂振华，E-mail: niezhenhua@163.com

Localized lymphomatoid papulosis: a case report

DONG Lingling1, ZHANG Weikun1, KONG Xiangjun2, NIE Zhenhua2   

  1. 1 Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China; 2 Department of Dermatology, Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin 300120, China
  • Online:2020-09-15 Published:2020-08-21
  • Contact: NIE Zhenhua, E-mail: niezhenhua@163.com

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摘要： 患者，女，48岁。右下肢散在红色结节、破溃反复发作3年。组织病理示：异型单一核细胞散在或簇状分布，淋巴细胞、炎性细胞大致呈楔形生长。免疫组化染色结果示CD30(+)、CD4(+)。诊断：局限型淋巴瘤样丘疹病A型。

关键词: 淋巴瘤样丘疹病, 局限型

Abstract: A 48-year-old female presented with red nodules and recurrent ulceration on the right lower limb for 3 years. Biopsy showed scattered or cluster distribution of heterocyst, lymphocytes and inflammatory cells with a wedge-shaped growth. Immunohistochemistry demonstrated that the staining of CD30 and CD4 were positive. The diagnosis of localized lymphomatoid papulosis type-A was made.

Key words: lymphomatoid papulosis, localized type