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先天性或后天性单侧痣样星状毛细血管扩张症。约5例(作者译)

[Congenital or acquired unilateral nevoid stellar telangiectasias. About 5 cases (author's transl)].

作者信息

Grupper C, Bermejo D, Bouyx P, Belperron P, Verret J L, Schnitzler L

出版信息

Ann Dermatol Venereol. 1978 Aug-Sep;105(8-9):691-7.

PMID:736437
Abstract

Based on five personal cases (one neo-natal case, one in childhood, and three cases in pregnant women) and sixteen published cases, this study remind us of the essential caracteristics of unilateral nevoid telangiectasis. Prevalence in women is noticeable appearance during pregnancy, with complete regression during post-partum, is quasi constant. If their nosological place is not clear among the essential telangiectasias, they seem to be quite different from Hutchinson's serpiginious angioma (verrucous telangiectasis), from Osler-Rendu's disease, from Brocq's telangiectasias and from generalizated telangiectasias. The true signification of all these diseases is still completely unknown.

摘要

基于5例个人病例(1例新生儿病例、1例儿童病例和3例孕妇病例)以及16例已发表病例,本研究使我们想起了单侧痣样毛细血管扩张的基本特征。女性患病率较高,在孕期明显出现,产后完全消退,情况基本一致。如果它们在原发性毛细血管扩张中的疾病分类位置不明确,那么它们似乎与哈钦森匐行性血管瘤(疣状毛细血管扩张)、奥斯勒-伦杜病、布罗克毛细血管扩张以及泛发性毛细血管扩张有很大不同。所有这些疾病的真正意义仍然完全未知。

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1
[Congenital or acquired unilateral nevoid stellar telangiectasias. About 5 cases (author's transl)].先天性或后天性单侧痣样星状毛细血管扩张症。约5例(作者译)
Ann Dermatol Venereol. 1978 Aug-Sep;105(8-9):691-7.
2
[Acquired nevoid telangiectasia (author's transl)].
Dermatologica. 1979;159(6):489-94.
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Unilateral nevoid telangiectasia syndrome: a case report and review of the literature.单侧痣样毛细血管扩张综合征:一例病例报告及文献复习
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[Sclerodermiform, plaque-like essential telangiectasias].[硬皮病样、斑块状原发性毛细血管扩张症]
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[Ultrastructural study of hereditary benign telangiectasia. Differential diagnosis from Osler Rendu disease].
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