中华皮肤科杂志 ›› 2016, Vol. 49 ›› Issue (8): 555-557.

• 论著 • 上一篇    下一篇

皮脂腺瘤31例临床病理分析

顾黎雄1,张德志2,吴晓琰1,邵雪宝3,李阿梅4,杨圣菊1,曹双林1,1,1,陈晓栋5,陈浩3   

  1. 1. 南通大学附属医院
    2. 新疆维吾尔自治区人民医院
    3. 南京 中国医学科学院北京协和医学院皮肤病研究所
    4. 南京市 中国医学科学院皮肤病研究所
    5. 南通大学附属医院皮肤科
  • 收稿日期:2015-10-22 修回日期:2016-01-05 发布日期:2016-08-05
  • 通讯作者: 张德志 E-mail:zdz-163@163.com
  • 基金资助:

    江苏省临床医学科技专项

Sebaceoma: a clinicopathological analysis of 31 cases

  • Received:2015-10-22 Revised:2016-01-05 Published:2016-08-05
  • Contact: Zhang DeZhi E-mail:zdz-163@163.com

摘要:

目的 对皮脂腺瘤进行临床病理分析。方法 回顾性分析31例皮脂腺瘤患者的临床病理资料,结合免疫组化,总结其临床病理学特征。结果 31例皮脂腺瘤中男9例,女22例,年龄(53.90 ± 15.40)岁,病程(9.41 ± 13.75)年,皮损位于面部者最常见,形态为丘疹,颜色分别呈红色、黄红色、正常肤色、淡褐色,大多无明显自觉症状。组织病理检查显示,肿瘤位于真皮内,所有肿瘤组织结构对称,其中9例与表皮相连。肿瘤细胞为基底样细胞及少许成熟皮脂腺细胞和部分过渡细胞,26例肿瘤组织中偶见成熟皮脂腺细胞(< 1%),2例成熟皮脂腺细胞 < 20%,3例成熟皮脂腺细胞占20% ~ 40%。5例部分区域偶见核分裂像。1例合并小汗腺汗孔瘤。31例均可见数量不等的导管。免疫组化结果显示,上皮膜抗原在皮脂腺瘤导管及成熟皮脂腺细胞全部呈阳性表达,上皮抗原在所有皮脂腺瘤中均不表达,20例皮脂腺瘤的导管癌胚抗原阳性,24例雄激素受体阳性,28例D2?40阳性。结论 皮脂腺瘤的诊断主要依靠组织病理检查。免疫组化检查抗上皮膜抗原抗体、抗雄激素受体抗体和D2?40的组合有利于与其他肿瘤鉴别。

Abstract:

Gu Lixiong, Zhang Dezhi, Wu Xiaoyan, Shao Xuebao, Li Amei, Yang Shengju, Cao Shuanglin, Chen Xiaodong, Chen Hao Department of Dermatology and Venerology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu, China (Gu LX, Wu XY, Yang SJ, Cao SL, Chen XD); Department of Dermatology, People′s Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830001, China (Zhang DZ); Department of Pathology, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China (Shao XB, Li AM, Chen H) Corresponding authors: Zhang Dezhi, Email: zdz?163@163.com; Chen Hao, Email: ch76ch@163.com 【Abstract】 Objective To analyze clinicopathologic features of sebaceoma. Methods Clinical, pathologic and immunohistochemical findings from 31 cases of sebaceoma were retrospectively analyzed. The clinicopathologic features of sebaceoma were investigated. Results There were 9 males and 22 females. The patients′ age was 53.90 ± 15.40 years, and the clinical course was 9.41 ± 13.75 years. Sebaceoma predominantly affected the face. The common lesion of sebaceoma was red, yellowish?red, skin?colored or slight brown papules, with no subjective symptoms in most cases. Histopathologically, neoplasms had symmetric structures, and were located in the dermis. Epidermal involvements were found in 9 cases. The neoplasm cells were mainly composed of basaloid cells, a few mature sebocytes and some transition cells. The proportion of mature sebocyts was less than 1% in 26 cases, less than 20% in 2 cases, and 20% - 40% in 3 cases. Mitoses were occasionally found in 5 cases. One patient was complicated by eccrine poroma. Varying amounts of ducts were found in all the patients. Immunohistochemical staining showed that epithelial membrane antigen was expressed on ducts and mature sebocytes in all the patients, while epithelial antigen was undetected in any of the patients. Carcinoembryonic antigen, androgen receptor and D2?40 were found in 20, 24 and 28 patients with sebaceoma, respectively. Conclusions The diagnosis of sebaceoma mainly depends on histopathological examination. Combined immunohistochemical detection of epithelial membrane antigen, androgen receptor and D2?40 is beneficial to its differential diagnosis.

引用本文

顾黎雄 张德志 吴晓琰 邵雪宝 李阿梅 杨圣菊 曹双林 陈晓栋 陈浩. 皮脂腺瘤31例临床病理分析[J]. 中华皮肤科杂志, 2016,49(8):555-557. doi: