A unique case report of bilateral spontaneous cerebrospinal fluid leak from bilateral sphenoid sinus skull base defects.

Journal of the colleges of medicine of South Africa Pub Date : 2026-03-20 eCollection Date: 2026-01-01 DOI:10.4102/jcmsa.v4i1.271
Divya P Ramyead Basant Rai, Lien Deschuytere, Darlene Lubbe
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Abstract

This brief report describes the presentation and management of a rare case of bilateral spontaneous cerebrospinal fluid (CSF) leaks resulting from skull base dehiscence in the sphenoid sinus lateral recess. A retrospective review of clinical data, including imaging and surgical interventions, was conducted. Informed consent was obtained. A middle-aged, obese woman presented with clear rhinorrhoea. Imaging identified bilateral encephaloceles and skull base defects. She underwent successful endoscopic surgery with fat grafts and septal flap repair, with no CSF leak recurrence at follow-ups.

Contribution: To our knowledge, this case is one of the few documented examples of bilateral spontaneous CSF leaks from skull base dehiscence in the sphenoid sinus. Endoscopic sinus surgery provides a minimally invasive, effective repair. Anatomical variations, such as extensive sphenoid sinus pneumatisation and congenital defects, combined with factors such as high body mass index, may predispose patients to spontaneous CSF leaks.

双侧蝶窦颅底缺损自发性脑脊液漏一例。
本文报告一例罕见的双侧自发性脑脊液(CSF)泄漏病例,由蝶窦外侧隐窝颅底裂开引起。回顾性回顾临床资料,包括影像学和手术干预。获得知情同意。中年肥胖妇女,有明显的鼻漏。影像学发现双侧脑膨出和颅底缺损。她接受了成功的内窥镜手术,脂肪移植和间隔皮瓣修复,随访时无脑脊液泄漏复发。贡献:据我们所知,本病例是少数记录的双侧自发性脑脊液渗漏的例子之一,来自于蝶窦颅底裂开。内窥镜鼻窦手术提供了微创,有效的修复。解剖变异,如广泛的蝶窦通气和先天性缺陷,加上高体重指数等因素,可能使患者易发生自发性脑脊液泄漏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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