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先天性硬脑膜静脉窦扩张合并多小脑回畸形的自发消退——病例报告

Spontaneous Resolution of Congenital Dural Venous Sinus Ectasia Associated With Polymicrogyria-Case Report.

作者信息

Kozłowska Zuzanna, Komasińska Paulina, Steinborn Barbara, Toboła-Wróbel Kinga, Pietryga Marek, Szymankiewicz-Breborowicz Marta, Szczapa Tomasz, Bekiesińska-Figatowska Monika

机构信息

Department of Neonatology, Neonatal Biophysical Monitoring and Cardiopulmonary Therapies Research Unit, Poznan University of Medical Sciences, Poznan, Poland.

Department of Developmental Neurology, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

Front Pediatr. 2022 Feb 28;10:822551. doi: 10.3389/fped.2022.822551. eCollection 2022.

Abstract

Dural venous sinus ectasia belongs to a rare group of venous sinus malformations of unknown origin and uncertain prognosis. We report the first patient with idiopathic congenital ectasia of the confluence of sinuses with thrombosis associated with bilateral polymicrogyria. It may highlight the causative relation between ischemia within the central nervous system due to torcular herophili ectasia with thrombosis in early pregnancy and the development of cortical malformations in neonates. We also highlight the role of MR neuroimaging in the diagnosis of these entities.

摘要

硬脑膜静脉窦扩张属于一组罕见的、病因不明且预后不确定的静脉窦畸形。我们报告了首例患有窦汇特发性先天性扩张并伴有血栓形成且与双侧多小脑回相关的患者。这可能凸显了妊娠早期由于窦汇扩张伴血栓形成导致的中枢神经系统缺血与新生儿皮质畸形发展之间的因果关系。我们还强调了磁共振神经成像在这些疾病诊断中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62c1/8918672/1d6d2b23fe23/fped-10-822551-g0001.jpg

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