Multiple non-familial trichoepitheliomas: A rare case and a review of the literature

F. Amaaoune, W. Zidane, M. Aksim, M. Aboudourib, O. Hocar, S. Amal
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引用次数: 0

Abstract

Trichoepitheliomas are benign tumors of follicular origin often appearing in childhood or early adolescence. They present as small, firm papulonodular lesions of normal skin color or translucent. The lesions gradually increase in size and then stabilize. They sit electively on the face, mainly on the nasolabial folds, forehead, chin, and cheeks, and sometimes on the scalp and neck. Trichoepitheliomas may be divided into three subgroups: multiple familial trichoepitheliomas, solitary non-hereditary trichoepitheliomas, and desmoplastic trichoepitheliomas. Non-familial multiple trichoepitheliomas are rarely described. Herein, we report the case of a twelve-year-old child whose clinical history and clinicopathologic correlation allowed us to retain the diagnosis of multiple non-familial trichoepitheliomas. Key words: Trichoepitheliomas; Sporadic; Genodermatosis; Cyld Gene; Anatomopathology
多发性非家族性毛上皮瘤:一例罕见病例及文献回顾
毛上皮瘤是起源于滤泡的良性肿瘤,常出现在儿童或青少年早期。它们表现为小而硬的丘疹样病变,皮肤颜色正常或半透明。病变逐渐增大,然后趋于稳定。它们有选择性地长在脸上,主要长在鼻唇沟、前额、下巴和脸颊上,有时也长在头皮和脖子上。毛上皮瘤可分为三个亚组:多发性家族性毛上皮瘤、单发性非遗传性毛上皮瘤和结缔组织增殖性毛上皮瘤。非家族性多发性毛上皮瘤很少被报道。在此,我们报告一个12岁儿童的病例,其临床病史和临床病理相关性允许我们保留多发性非家族性毛上皮瘤的诊断。关键词:毛上皮瘤;零星的;遗传性皮肤病;Cyld基因;Anatomopathology
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