表皮-皮脂腺痣综合征  

Schimmelpenning syndrome:a case report

作　　者：张斌[1] 杨海珍[1] 陈喜雪[1] 陈伟[1] 伦文辉[2] 涂平[1] 

机构地区：[1]北京大学第一医院皮肤性病科,北京100034 [2]北京大学北京地坛医院皮肤性病科,北京100015

出　　处：《临床皮肤科杂志》2010年第7期434-435,共2页Journal of Clinical Dermatology

摘　　要：报告1例年龄较小的表皮-皮脂腺痣综合征。患儿女,95 d。左侧头面颈部淡褐色片状疣状增殖性皮损95 d,间断抽搐15 d。头皮中线前囟门处毛发脱失区,表面无毛发。左眼外侧巩膜囊性增生物向内延伸至角膜,呈云翳状改变。头颅磁共振成像(MRI)示左侧颞叶蛛网膜囊肿。A case of younger Schimmelpenning syndrome is reported. A 95-day-old female child presented with a dark brown verrucous hyperplasia in a linear on her scalp, face and neck at birth and with epileptic fits for 15 days. There was an alopecia area on the anterior fontanelle. Eye examination showed a cystoid neoplasm of selera extending to cornea on the inner canthus of her left eye. Nuclear magnetic resonance imaging of her head revealed araehnoid cysts in her temporal lobe. The diagnosis was made as Sehimmelpenning syndrome.

关 键 词：表皮-皮脂腺痣综合征 

分 类 号：R758.7[医药卫生—皮肤病学与性病学]