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先天性大理石样皮肤血管扩张症(作者译)

[Cutis marmorata telangiectatica congenita (author's transl)].

作者信息

Pérez Alvarez F, García-Tornel S, Noguera X

出版信息

An Esp Pediatr. 1981 Nov;15(5):488-91.

PMID:7332153
Abstract

Authors report a new case of cutis marmorata telangiectatica congenita. This disease has been preferably described by dermatologists and few issues in the pediatrics literature have been published. This is a rare illness recognizable at birth which must be knowed by pediatricians to establish the diagnosis and prognosis in the beginning. A new case with typical features is presented being of localized distribution and having as associated abnormalities. Hemiatrophy, enlarged inferior extremity without Klippel-Trenaunay syndrome and physical growth retardation.

摘要

作者报告了一例先天性大理石样皮肤毛细血管扩张症的新病例。这种疾病主要由皮肤科医生描述,儿科文献中发表的相关内容较少。这是一种出生时即可识别的罕见疾病,儿科医生必须了解它以便在早期做出诊断和判断预后。本文呈现了一例具有典型特征的新病例,其病变呈局限性分布,并伴有相关异常。半身萎缩、下肢粗大但无克-特综合征以及身体发育迟缓。

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