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先天性全毛囊痣伴多指畸形。

Congenital panfollicular nevus associated with polydactyly.

作者信息

Kim Jinah, Zambrano Eduardo V, McNiff Jennifer M

机构信息

Department of Pathology, Yale University School of Medicine, New Haven, CT, USA.

出版信息

J Cutan Pathol. 2007 Dec;34 Suppl 1:14-7. doi: 10.1111/j.1600-0560.2006.00714.x.

Abstract

A 2-year-old girl presented with ulnar-sided duplication of the left thumb distal to the interphalangeal joint and syndactyly of the first web space. She also had several asymptomatic pink-tan cutaneous papules, involving the first and second ray of the left hand and wrist, clinically resembling a linear epidermal nevus. Microscopically, the papules were composed of well-circumscribed aggregates of basaloid epithelium within the dermis. No normal hair follicles were identified. Follicular germ and papillae were identified, representing abortive attempts at hair follicle formation. The features were remarkably similar to a novel entity described by Finn and Argenyi as congenital panfollicular nevus. In our case, the congenital panfollicular nevus was associated with distal thumb polysyndactyly, which may suggest an important link between limb patterning and hair follicle development.

摘要

一名2岁女童,其左拇指在指间关节远端尺侧重复畸形,且第一蹼间隙并指。她还有几个无症状的粉褐色皮肤丘疹,累及左手和手腕的第一和第二射线,临床上类似线状表皮痣。显微镜下,丘疹由真皮内界限清楚的基底样上皮聚集而成。未发现正常毛囊。发现了毛囊胚芽和乳头,代表毛囊形成的失败尝试。这些特征与Finn和Argenyi描述的一种新实体——先天性全毛囊痣非常相似。在我们的病例中,先天性全毛囊痣与拇指远端多指并指相关,这可能提示肢体模式形成与毛囊发育之间存在重要联系。

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