Rato Margarida, Filipe Monteiro Ana, Aranha João, Tavares Ermelindo
Department of Dermatology, Hospital de Santarém EPE, Santarém, Portugal.
Dermatol Online J. 2017 Jun 15;23(6):13030/qt67m6h7tb.
A healthy 31-year-old woman presented with a 20-year history of asymptomatic skin-colored papules and nodules on the central area of the face. Her maternal grandmother, aunts, mother, and sister also had similar lesions. Clinical, histopathological, and genetic features allowed the diagnosis of multiple familial trichoepithelioma. The patient and family were referred to the genetic department for genetic counselling. Close follow-up for the possibility of secondary basal cell carcinoma is warranted.
一名31岁健康女性，面部中央出现无症状肤色丘疹和结节已有20年病史。她的外祖母、姨妈、母亲和姐姐也有类似病变。临床、组织病理学和遗传学特征确诊为多发性家族性毛发上皮瘤。患者及其家属被转介到遗传科进行遗传咨询。有必要密切随访，观察是否有继发基底细胞癌的可能。
