中国麻风皮肤病杂志 ›› 2023, Vol. 39 ›› Issue (6): 429-430.doi: 10.12144/zgmfskin202306429

• 病例报告 • 上一篇    下一篇

头皮血管肉瘤一例

方梦1，2,冉德琳2,周桂芝2,刘永霞2,杨宝琦2,王广进2   

  1. 1山东大学，济南，250014；
    2山东第一医科大学附属皮肤病医院（山东省皮肤病医院），山东省皮肤病性病防治研究所，济南，250022
  • 出版日期:2023-06-15 发布日期:2023-05-18

Scalp angiosarcoma: a case report

FANG Meng1,2, RAN Delin2, ZHOU Guizhi2, LIU Yongxia2, YANG Baoqi2, WANG Guangjin2   

  1. 1 Shandong University, Jinan 250014, China;
    2 Shandong Provincial Hospital for Skin Diseases & Shandong Provincial Institute of Dermatology and Venereology, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250022, China
  • Online:2023-06-15 Published:2023-05-18

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摘要： 患者，男，68岁。头皮部褐色结节8个月，扩散并破溃3个月。组织病理示：真皮内可见不规则血管腔形成，有明显异型性的肥大内皮细胞，提示血管肉瘤。免疫组化示：CD31（+）、CD34（+）、D2-40（+）、HHV8（-）。临床诊断：头皮血管肉瘤。

关键词: 血管肉瘤, 头皮部

Abstract: A 68-year-old male presented with brown nodules on the scalp for 8 months, spread and ruptured for 3 months. Pathology showed that irregular vascular lumen formation in the epidermis and hypertrophic endothelial cells with obvious atypia, suggesting angiosarcoma. Immunohistochemistry showed CD31 (+), CD34 (+), D2-40 (+), HHV8 (-). The diagnosis of scalp angiosarcoma was made.

Key words: angiosarcoma, scal