中国麻风皮肤病杂志 ›› 2019, Vol. 35 ›› Issue (4): 219-221.doi: 10.12144/zgmfskin201904219

• 论著 • 上一篇    下一篇

多核细胞血管组织细胞瘤一例并文献复习

王文娟  巴伟  孟宪芙  李承新   

  1. 解放军总医院皮肤科，北京,100853

  • 出版日期:2019-04-15 发布日期:2019-05-17
  • 通讯作者: 李承新，E-mail：chengxinderm@163.com

One case of Multinucleate cell angiohistiocytoma and review of the literature

WANG Wenjuan, BA Wei, MENG Xianfu, LI Chengxin   

  1. Department of Dermatology, PLA General Hospital, Beijing 100853, China
  • Online:2019-04-15 Published:2019-05-17
  • Contact: LI Chengxin, E-mail：chengxinderm@163.com

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摘要： 患者，男, 62 岁。因右手背丘疹、结节就诊。皮损组织病理检查示：真皮浅中部有较多增生的薄壁小血管，真皮内胶原增生性改变，真皮胶原纤维束间散在组织细胞和有棘突的多核细胞，CD68阳性，结合临床、组织病理改变和免疫组化染色可明确诊断为多核细胞血管组织细胞瘤。我们报道国内第3例典型病例，以提高对该病的认识，并通过文献回顾阐明这一疾病的临床和组织病理学特征。

关键词: 多核巨细胞, 血管组织细胞瘤

Abstract: One 62-year-old male presented with papules and nodules on the back of right hand. The histological features characterized by dermal vascular proliferation, collagen proliferative changes in dermis, lymphohistiocytic infiltrate and bizarre multinucleate cells， positivity of CD68. Combined with the clinical, histopathological changes and immunohistochemical staining, the diagnosis of MCAH was made. We report the third typical case in China, to raise awareness of the disease. The literatures of clinical and histopathological features of this disease were  reviewed.

Key words: multinucleate, angiohistiocytoma