节点文献

乳头状汗管囊腺瘤5例临床病理学分析

Syringocystadenoma papilliferum: a clinicopathological and immunohistochemical study of 5 cases

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 沈宏王一玲施桂芬许爱娥

【Author】 Shen Hong, Wang Yiling, Shi Guifen, Xu Ai’e (Department of Dermatology, the Third Hospital of Hangzhou City, Hangzhou 310009)

【机构】 杭州市第三医院皮肤科杭州市第三医院皮肤科 杭州310009杭州310009杭州310009

【摘要】 目的 探讨乳头状汗管囊腺瘤 (SCAP)的临床病理特征和诊断要点。方法 分析 5例SCAP临床资料 ,观察其组织学形态及免疫表型特征。结果 本组男 4例、女 1例 ;发病年龄 0~ 14岁 ,临床上皮损表现为数个丘疹呈线状排列或孤立性结节、斑块。组织学特征 :大小不一的乳头状突起衬以两层上皮细胞。免疫表型 :SCAP绝大多数内层柱状细胞CK7、CK19阳性 ,外层立方细胞CK5 / 8、CK7阳性。结论 SCAP是一种少见的良性皮肤错构瘤 ,鉴别诊断包括乳头状汗腺囊腺瘤、管状大汗腺腺瘤。

【Abstract】 Purpose To explore the clinicopathological features and diagnosis of syringocystadenoma papilliferum(SCAP). Methods Five cases of CSAP were analyzed by means of clinicopathologic date,histopathologic features,immunohistochemical technique. Results There were four males and one female, with age ranged 0~14 years. Clinically,the lesions of the skin consisted of one to several papules occurring in a liner fasion or as a solitary nodule and plaque. Microscopically, the distinctive feature was the presence of papillary processes of various sizes lined with two epithelial cell layers. Immumohistochemically, the columnar cells of the tumour were mostly positive for CK7 and CK19. The cuboidal cells of the tumor expressed CK5/8 and CK7. Conclusions SCAP is a rare benign hamartomatous tumour of the skin.The differential diagnosis of SCAP includes hidradenoma papilliferum and tubular apocrine adenoma.

  • 【文献出处】 临床与实验病理学杂志 ,Chinese Journal of Clinical and Experimental Pathology , 编辑部邮箱 ,2004年04期
  • 【分类号】R739.5
  • 【被引频次】7
  • 【下载频次】135
节点文献中: 

本文链接的文献网络图示:

本文的引文网络