The Case of the Rare Malformation and Rare Variant: An Infant with a Self-Embolized Torcular Dural Sinus Malformation and a Concomitant Prothrombin Variant.

Child neurology open Pub Date : 2022-11-28 eCollection Date: 2022-01-01 DOI:10.1177/2329048X221140784
Roxanne M Miller, Anthony Zarka, Samiya F Ahmad
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引用次数: 0

Abstract

Torcular dural sinus malformations (tDSMs) can occur in the brain during prenatal development. These rare vascular malformations occur in less than 1% of the population but can lead to a poor prognosis secondary to congestive heart failure and hydrocephalus. Many tDSM cases require surgical embolization or coiling to return normal cerebral blood flow and prevent mortality and morbidity. We describe the first case of spontaneous self-embolization of a large torcular dural sinus malformation, possibly due to hypercoagulability from a comorbid prothrombin gene variant. Despite a grim prognosis at birth, the child is alive and thriving at age 3, with only mild speech delay.

Abstract Image

Abstract Image

罕见畸形及罕见变异一例:婴儿自栓塞性硬脑膜环窦畸形及伴随的凝血酶原变异。
圆形硬脑膜窦畸形(tDSMs)可发生在大脑产前发育。这些罕见的血管畸形发生在不到1%的人口,但可导致预后不良继发充血性心力衰竭和脑积水。许多tDSM病例需要手术栓塞或盘绕,以恢复正常的脑血流,防止死亡和发病率。我们描述了第一例自发的自我栓塞的大圆形硬脑膜窦畸形,可能是由于高凝从合病凝血酶原基因变异。尽管出生时的预后很糟糕,但这个孩子在3岁时还活着,发育良好,只有轻微的语言障碍。
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