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先天性大理石样皮肤毛细血管扩张症:长期随访、文献综述及合并先天性甲状腺功能减退症的病例报告

Cutis marmorata telangiectatica congenita: long-term follow-up, review of the literature, and report of a case in conjunction with congenital hypothyroidism.

作者信息

Pehr K, Moroz B

机构信息

Division of Dermatology, McGill University, Montreal Children's Hospital.

出版信息

Pediatr Dermatol. 1993 Mar;10(1):6-11. doi: 10.1111/j.1525-1470.1993.tb00002.x.

DOI:10.1111/j.1525-1470.1993.tb00002.x
PMID:8493172
Abstract

Cutis marmorata telangiectatica congenita is an uncommon, generally congenital, cutaneous condition. The major skin findings are persistent, fixed cutis marmorata, telangiectasia, and phlebectasia; often, there is associated skin atrophy and ulceration as well. Significantly, two-thirds of patients have other congenital anomalies, although often minor ones. We report a series of eight children with cutis marmorata telangiectatica congenita, including one with associated congenital hypothyroidism, a relationship that has never before been noted.

摘要

先天性大理石样皮肤毛细血管扩张症是一种罕见的、通常为先天性的皮肤疾病。主要的皮肤表现为持续性、固定性的大理石样皮肤、毛细血管扩张和静脉扩张;通常还伴有皮肤萎缩和溃疡。值得注意的是,三分之二的患者有其他先天性异常,尽管通常较为轻微。我们报告了一系列8例先天性大理石样皮肤毛细血管扩张症患儿,其中1例伴有先天性甲状腺功能减退,这种关联此前从未被提及。

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