一名患有唐氏综合征的女孩出现穿通性粟丘疹样特发性皮肤钙化症和眶周汗管瘤。
Perforating milia-like idiopathic calcinosis cutis and periorbital syringomas in a girl with Down syndrome.
作者信息
Schepis C, Siragusa M, Palazzo R, Batolo D, Romano C
机构信息
Department of Pediatrics, OASI Institute (IRCCS), Troina, Italy.
出版信息
Pediatr Dermatol. 1994 Sep;11(3):258-60. doi: 10.1111/j.1525-1470.1994.tb00598.x.
Abstract
An 11-year-old girl with Down syndrome had whitish, milia-like lesions on the acral areas of the limbs, and periorbital syringomas. Calcium deposits were the histologic counterparts of the milia-like lesions. This is the first European report of this feature in Down syndrome.
摘要
一名患有唐氏综合征的11岁女孩，其四肢末端部位出现了类似粟丘疹的白色皮损，且眶周有汗管瘤。组织学检查显示，钙沉积是这些类似粟丘疹皮损的对应表现。这是欧洲首例关于唐氏综合征出现此特征的报告。
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