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先天性单侧痣样毛细血管扩张症1例 被引量:2

A Case of Congenital Unilateral Nevoid Telangiectasia
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摘要 患儿男,8岁,左下肢、左臀和左背部毛细血管扩张4年余。皮肤科情况:上述部位多发毛细血管扩张,皮损呈单侧带状分布。皮损组织病理示:表皮大致正常,真皮浅层见毛细血管扩张伴少量红细胞渗出;免疫组织化学:Giemsa染色(-)。诊断:先天性单侧痣样毛细血管扩张。 An 8-year-old boy presented telangiectasia on the left lower extremity,the left buttock and the left back for more than four years.Physical examination revealed multiple telangiectases distributed in a zoster and unilateral pattern,involving the above-mentioned sites.Histological examination showed that epidermis was normal,and dilatated capillary vessels in the superficial dermis with minimal erythrocyte exosmosis.Immunohistochemistry showed that the Giemsa′s staining was negative.A diagnosis of congenital unilateral nevoid telangiectasia was made.
作者 肖学敏 彭佳美 康洁 林艳艳 林立航 XIAO Xuemin;PENG Jiamei;KANG Jie;LIN Yanyan;LIN Lihang(Department of Dermatology,Union Hospital,Fujian Medical University,Fuzhou 350001,China;Department of Dermatology,the First Affiliated Hospital,Fujian Medical University,Fuzhou 350005,China)
出处 《中国皮肤性病学杂志》 CAS CSCD 北大核心 2020年第9期1054-1055,共2页 The Chinese Journal of Dermatovenereology
基金 国家自然科学基金(81602785) 福建省自然科学基金(131750422017J05128) 福建省卫生健康中青年骨干人才培养项目(2019-ZQN-47) 福建中医药大学科研平台校管课题(X2018018-平台)。
关键词 痣样毛细血管扩张症 先天性 单侧 Nevoid telangiectasia congenital unilateral
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  • 1Dadlani C, Kamino H, Waiters RF, et ai. Unilateral nevoid telangiectasia [ J ]. Dermatol Online J,2008, 14 ( 10 ) : 3.
  • 2Wenson SF, Jan F, Sepehr A. Unilateral nevoid telangiectasia syndrome: a case report and review of the literature[ J]. Dermatol Online J,2011,17(5) :2.
  • 3Akman-Karaka- A, Kandemir H, Senol U, et al. Unilateral nevoid telangiectasia Accompanied by neurological disorders [ J ]. J Eur Acad Dermatol Venereol,2011,25 ( 11 ) : 1356 - 1359.
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