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先天性大理石样皮肤血管扩张症

Cutis marmorata telangiectatica congenita.

作者信息

Garzon Maria C, Schweiger Eric

机构信息

Departments of Dermatology and Pediatrics, Columbia University, New York, NY 10032, USA.

出版信息

Semin Cutan Med Surg. 2004 Jun;23(2):99-106. doi: 10.1016/j.sder.2004.01.003.

Abstract

Cutis marmorata telangiectatica congenita is an uncommon vascular malformation composed of capillary and venous sized vessels. It presents with a distinct reticulated pattern that is reminiscent of physiologic cutis marmorata however skin lesions do not resolve with warming of the skin surface. It may have a localized or generalized pattern on the skin. Associated anomalies occur in individuals with cutis marmorata telangiectatica congenita the most commonly reported are limb asymmetry and the coexistence of other vascular birthmarks. Adams Oliver Syndrome and cutis marmorata telangiectatica congenital-macrocephaly syndrome are rare disorders that are associated with cutis marmorata telangiectatica congenita.

摘要

先天性大理石样皮肤毛细血管扩张症是一种罕见的血管畸形,由毛细血管和静脉大小的血管组成。它呈现出独特的网状图案,让人联想到生理性大理石样皮肤,然而皮肤病变不会随着皮肤表面温度升高而消退。它在皮肤上可能呈现局部或全身性分布。先天性大理石样皮肤毛细血管扩张症患者可能伴有相关异常,最常报道的是肢体不对称以及其他血管性胎记并存。亚当斯-奥利弗综合征和先天性大理石样皮肤毛细血管扩张症-巨头综合征是与先天性大理石样皮肤毛细血管扩张症相关的罕见疾病。

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