Mataix J, Bañuls J, Botella R, Laredo C, Lucas A
Servicio de Dermatología, Hospital General Universitario de Alicante, Spain.
Actas Dermosifiliogr. 2006 Dec;97(10):669-72. doi: 10.1016/s0001-7310(06)73492-5.
The Brooke-Spiegler syndrome is a rare, autosomally dominant disease with a predisposition to develop different adnexal tumors. Clinically it is characterized by the presence of multiple cylindromas, trichoepitheliomas, and occasionally, spiradenomas. Although Brooke-Spiegler syndrome, familial cylindromatosis and multiple familial trichoepithelioma were initially described as separate entities, the recently identified identical mutations in the gene of cylindromatosis suggest that they represent fenotypic variations of the same entity. In this article we present the case of a woman and her daughter, both affected by this rare genodermatosis.
布鲁克-施皮格勒综合征是一种罕见的常染色体显性疾病,易发生不同的附件肿瘤。临床上,其特征为存在多个圆柱瘤、毛发上皮瘤,偶尔还会出现汗腺螺旋腺瘤。尽管布鲁克-施皮格勒综合征、家族性圆柱瘤病和多发性家族性毛发上皮瘤最初被描述为不同的疾病实体,但最近在圆柱瘤病基因中发现的相同突变表明,它们代表同一疾病实体的不同表型变异。在本文中,我们介绍了一位女性及其女儿均患有这种罕见遗传性皮肤病的病例。