中国麻风皮肤病杂志 ›› 2024, Vol. 40 ›› Issue (9): 630-633.doi: 10.12144/zgmfskin202409630

• 临床研究 • 上一篇    下一篇

母细胞性浆细胞样树突细胞肿瘤一例并文献复习

李晗,丁高中,孙澜   

  1. 南京医科大学附属苏州医院,苏州市立医院东区皮肤科，江苏苏州，215000
  • 出版日期:2024-09-15 发布日期:2024-08-14

Blastic plasmacytoid dendritic cell tumor: a case report and literature review

LI Han, DING Gaozhong, SUN Lan   

  1. Department of Dermatology, the Affiliated Suzhou Hospital of Nanjing Medical University, East District of Suzhou Municipal Hospital, Suzhou 215000, China
  • Online:2024-09-15 Published:2024-08-14

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摘要： 母细胞性浆细胞样树突细胞肿瘤恶性程度极高，多以皮肤为首发表现，皮损表现多样，易误诊漏诊，诊断需结合广泛的免疫表型和组织病理学特点，易复发，预后不良。我院诊治1例76岁老年男性患者，以头颈部暗紫色浸润性结节和肿块为首发表现。免疫表型和组织病理学特点符合母细胞性浆细胞样树突细胞肿瘤。

关键词: 母细胞性浆细胞样树突细胞肿瘤, 皮肤肿瘤, 免疫表型, 临床病理表现

Abstract: Blastic plasmacytoid dendritic cell tumor is extremely malignant, the skin is the first manifestation of the disease, and the manifestations of skin lesions are diverse, which is easy to be misdiagnosed and missed diagnosed. The diagnosis of this disease requires a multiple immunophenotypys and histopathological features. It is prone to relapse and has a poor prognosis. A 76-year-old male patient presented with dark-purple invasive nodules and masses on the head and neck as the first manifestation. The immunophenotypic and histopathological features were in accordance with blastic plasmacytoid dendritic cell tumor.

Key words: blastic plasmacytoid dendritic cell neoplasm, skin neoplasms, immunophenotype, clinicopathologic features