Johnson Hillary, Robles Mirin, Kamino Hideko, Walters Ruth F, Lee Arnold, Sanchez Miguel
Department of Dermatology, New York University, USA.
Dermatol Online J. 2008 Oct 15;14(10):5.
A 29-year-old man presented with a long-standing history of asymptomatic, skin-colored, facial papules and nodules. Histopathologic examination of a representative papule demonstrated trichoepithelioma. The patient had a history of a brother with a similar phenotype, which suggests a diagnosis of familial trichoepithelioma. Linkage and mutational analyses support genetic heterogeneity of familial trichoepithelioma, possibly sharing a clinical spectrum with Brooke-Spiegler syndrome and familial cylindromatosis since each entity has been associated with mutations the CYLD gene.
一名29岁男性,有长期无症状的肤色面部丘疹和结节病史。对一个代表性丘疹进行组织病理学检查显示为毛发上皮瘤。该患者有一个兄弟有类似的表型,这提示为家族性毛发上皮瘤的诊断。连锁分析和突变分析支持家族性毛发上皮瘤的基因异质性,它可能与布鲁克-施皮格勒综合征和家族性圆柱瘤有共同的临床谱,因为每个实体都与CYLD基因突变有关。