结节性硬化症中的局限性厚皮性多指（趾）畸形

Localized pachydermodactyly in tuberous sclerosis.

作者信息

Lo W L, Wong C K

机构信息

Department of Dermatology, National Yang-Ming Medical College, Taipei, Taiwan, Republic of China.

出版信息

Clin Exp Dermatol. 1993 Mar;18(2):146-7. doi: 10.1111/j.1365-2230.1993.tb00997.x.

DOI:10.1111/j.1365-2230.1993.tb00997.x

PMID:8481991

Abstract

Pachydermodactyly refers to a rare form of digital fibromatosis involving the proximal portions of the fingers. There are only nine cases reported in the literature, all idiopathic and occurring in young men. We report a 5-year-old Chinese boy with tuberous sclerosis who presented with localized pachydermodactyly since birth. This congenital form of pachydermodactyly may represent an additional cutaneous sign of tuberous sclerosis.

摘要

厚皮性多指（趾）畸形是一种罕见的指（趾）纤维瘤病，累及手指近端。文献中仅报道了9例，均为特发性，且发生于年轻男性。我们报告了一名5岁的中国男孩，患有结节性硬化症，自出生以来就出现局限性厚皮性多指（趾）畸形。这种先天性厚皮性多指（趾）畸形可能是结节性硬化症的另一种皮肤表现。