蝶窦外侧脑膜脑膨出显示皮质发育畸形1例。

NMC Case Report Journal Pub Date : 2022-09-03 eCollection Date: 2022-01-01 DOI:10.2176/jns-nmc.2022-0152
Taro Sato, Tetsuya Hiraishi, Mari Tada, Manabu Natsumeda, Jotaro On, Haruhiko Takahashi, Taiki Saito, Noritaka Okubo, Makoto Oishi, Akiyoshi Kakita, Yukihiko Fujii
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引用次数: 0

摘要

侧蝶窦(SS)的脑膜脑膨出已被确定为一种罕见的实体,通常由脑脊液(CSF)鼻漏检测到。迄今为止,在许多病例中,SS外侧脑膜脑膨出的病理仍不清楚。在这项研究中,我们报告了一例72岁的女性动静脉畸形谁提出脑脊液鼻漏。放射学检查显示SS外侧有左侧颞部脑膜脑膨出。我们切除了脑膜脑膨出并进行了颅底修复,之后脑脊液鼻漏得以解决。病理检查显示先天性皮质异常,神经元形状各异,后天性慢性组织改变,包括原纤维胶质瘤和罗森塔尔纤维散在。这些发现可能有助于进一步了解SS侧脑膜脑膨出的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Meningoencephalocele in the Lateral Sphenoid Sinus Showing Malformation of Cortical Development: A Case Report.

Meningoencephalocele in the Lateral Sphenoid Sinus Showing Malformation of Cortical Development: A Case Report.

Meningoencephalocele in the Lateral Sphenoid Sinus Showing Malformation of Cortical Development: A Case Report.

Meningoencephalocele in the Lateral Sphenoid Sinus Showing Malformation of Cortical Development: A Case Report.

Meningoencephalocele in the lateral sphenoid sinus (SS) has been determined to be a rare entity often detected by cerebrospinal fluid (CSF) rhinorrhea. To date, the pathology of meningoencephalocele in the lateral SS has remained to be unclear in many cases. In this study, we report on a case of a 72-year-old woman with an arteriovenous malformation who presented with CSF rhinorrhea. Radiologic investigations revealed a left temporal meningoencephalocele in the lateral SS. We removed the meningoencephalocele and performed skull base repair, after which the CSF rhinorrhea resolved. Pathological examination showed congenital cortical abnormalities with dysmorphic neurons in various shapes and acquired chronic tissue alterations including fibrillary gliosis and scattered Rosenthal fibers. These findings may further aid in understanding the etiopathogenesis of meningoencephalocele in the lateral SS.

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