家族性厚皮性指节垫病。

Familial pachydermodactyly.

作者信息

Russo F, Rodriguez-Pichardo A, Camacho F

机构信息

Department of Medical Surgical Dermatology and Venereology, University of Seville School of Medicine, Spain.

出版信息

Acta Derm Venereol. 1994 Sep;74(5):386-7. doi: 10.2340/0001555574386387.

DOI:10.2340/0001555574386387

PMID:7817679

Abstract

Pachydermodactyly is a rare form of digital fibromatosis. There are only 15 cases reported in the literature, all with a negative family history. Only one of the previously reported cases was a woman. We now report 2 female cases, mother and daughter, who, to the best of our knowledge, are the first patients with familial pachydermodactyly. The histological evolution of this disease over the years had not been previously reported.

摘要

厚皮性多指（趾）纤维瘤病是一种罕见的指（趾）纤维瘤病形式。文献中仅报道了15例，均无家族史。先前报道的病例中只有1例为女性。我们现在报告2例女性病例，母亲和女儿，据我们所知，她们是首例家族性厚皮性多指（趾）纤维瘤病患者。多年来这种疾病的组织学演变此前尚未见报道。