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首页> 外文期刊>International Journal of Trichology >A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
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A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features

机译:先天性膜性发育不良和皮肤镜特征

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Membranous, bullous, or cystic aplasia cutis congenita is a clinical subtype of aplasia cutis, covered with a membranous or glistening surface. A male newborn presented at birth with two flat lesions on the left parietal scalp, surrounded by a rim of terminal hairs. Physical examination revealed two translucent papules. On dermoscopy, they showed a reddish background, thin, lineal vessels and, remarkably few hair bulbs could be seen because of the translucency of the lesion. No skull bone and brain defects were found. The diagnosis of membranous aplasia cutis congenita was established. Histologically, it is characterized by an atrophic epidermis with loose fibrovascular stroma and edematous dermal stroma. Dermoscopy may help to rule out other entities (herpes simplex, epidermolysis bullosa, trauma…) since the atrophic epidermis and fibrovascular stroma is evidenced by the hair bulbs and its characteristic translucency (“translucency's sign”). Key words: Aplasia cutis, child, dermoscopy, membranous
机译:先天性膜性,大疱性或囊性发育不全是皮肤发育不全的临床亚型,覆盖有膜状或有光泽的表面。男性刚出生时,左顶头皮上有两个扁平的病灶,周围有末端毛的边缘。体格检查发现两个半透明丘疹。在皮肤镜检查中,它们显示出淡红色的背景,细而直的血管,并且由于病灶的半透明性,几乎看不到毛发。没有发现头骨和脑部缺损。建立了先天性膜性发育不良的诊断。从组织学上看,其特征是萎缩的表皮,纤维血管基质松散,皮肤水肿。皮肤镜检查可能有助于排除其他实体(单纯疱疹,大疱性表皮松解,创伤……),因为萎缩性表皮和纤维血管基质由鳞茎及其特征性的半透明性(“半透明性体征”)证明。关键词:皮肤发育不良,儿童,皮肤镜,膜性

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