儿童一例与泰克相关的畸形和类马氏体质:偶然发现还是特征?

Pub Date : 2022-01-01
P S Buonuomo, M El Hachem, G Mastrogiorgio, E Pisaneschi, A Diociaiuti, I Rana, M Macchiaiolo, R Capolino, M V Gonfiantini, D Vecchio, A Novelli, A Bartuli
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引用次数: 0

摘要

血管畸形包括范围广泛的复杂血管病变。由于临床表现的极端可变性,分类及其相关综合征提出了一个挑战。在这里,我们描述了一个病例的男孩表现为马凡样体质,皮肤血管畸形,和严重的急性贫血,由于回肠静脉畸形。虽然马凡氏表型的一组遗传标记为阴性,但我们在患者的TEK基因中发现了一个新生突变。本病例支持扩展tek相关血管畸形的表型谱。
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A pediatric case of TEK-Related malformations and marfanoid habitus: an incidental finding or a feature?

Vascular malformations encompass a wide range of complex vascular lesions. Due to the extreme variability of clinical presentation, classification and their related syndromes presents a challenge. Here we describe a case of a boy presenting with Marfanoid habitus, cutaneous vascular malformations, and severe acute anemia due to ileal venous malformations. Although a panel of genetic markers for the Marfan phenotype was negative, we identified a de novo mutation in the TEK gene in the patient. This case supports expansion of the phenotypic spectrum of TEK-related vascular malformations.

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