不同影像学表型的萎缩性头枕炎——病例系列及文献综述。

IF 0.8 Q4 CLINICAL NEUROLOGY
Journal of Neurosciences in Rural Practice Pub Date : 2023-04-01 Epub Date: 2023-03-16 DOI:10.25259/JNRP_46_2022
Rajkumar Swathi Kiran, Vellathussery C Sunitha, Ravindar Kashyap, Ramachandran Madhan, Andi S Ramesh, Krishnan Nagarajan
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引用次数: 0

摘要

萎缩性脑脊髓炎(ACs)是一种先天性颅骨缺陷,颅内基本结构通过该缺陷突出,并与持续的镰状窦或直窦的胚胎定位有关。我们描述了5例ACs,其中只有一例具有胚胎直窦。3例患者有其他颅内畸形,如胼胝体发育不全、顶盖发育异常,另一例有顶枕多显微回畸形伴镰裂,第三例有额角畸形和皮质发育不良。AC的预后取决于共存的颅内异常,这突出了磁共振成像在诊断其他相关异常以预测预后和计划必要的手术治疗中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Atretic cephaloceles with different imaging phenotypes - Case series with review of literature.

Atretic cephaloceles with different imaging phenotypes - Case series with review of literature.

Atretic cephaloceles (ACs) are congenital skull defects with herniation of rudimentary intracranial structures through the defect and associated with persistent falcine sinus or embryonic positioning of straight sinus. We describe five cases of ACs, out of which only one had embryonic straight sinus. Three cases had other intracranial malformations such as hypoplasia of corpus callosum, dysplastic tectum in one child and parieto-occipital polymicrogyria with falcotentorial dehiscence in the other, and frontal horn deformity and cortical dysplasia in the third. The prognosis of AC depends on the coexistent intracranial abnormalities and this highlights the role of magnetic resonance imaging in diagnosing the other associated anomalies for prediction of prognosis and planning of necessary surgical management.

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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
129
审稿时长
22 weeks
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