Middle fossa approach for a petrous apex bony spur causing trigeminal neuralgia: illustrative case.

Forrest Hamrick, Samantha Colby, William T Couldwell, Shervin Rahimpour
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Abstract

Background: Trigeminal neuralgia (TN) can arise from trigeminal nerve compression at the root entry zone due to neurovascular conflict, which most often presents in the 6th decade of life. The authors report the case of a young patient with TN with a petrous apex bony spur near the entrance of Meckel's cave, causing compression of the proximal trigeminal nerve.

Observations: A 21-year-old woman presented with a 5-year history of progressive right-sided TN. Axial T2 sampling perfection with application optimized contrast using different flip angle evolution magnetic resonance imaging (MRI) did not reveal vascular compression of the trigeminal nerve. However, sagittal reformats demonstrated a prominent bony ridge along the petrous apex, causing compression of the right trigeminal nerve at the porus trigeminus. Removal of the bony spur via a middle fossa approach completely resolved the patient's symptoms.

Lessons: Although TN is most frequently caused by neurovascular compression, it is vital to examine the entire course of the trigeminal nerve on MRI to identify alternative causes of nerve compression in the absence of neurovascular conflict. Bony compression is a rare cause of TN that should be considered, particularly in younger patients. The presence of prominent osseous structures along the course of the trigeminal nerve can be evaluated reliably on sagittal MRI. https://thejns.org/doi/10.3171/CASE24321.

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中窝入路治疗引起三叉神经痛的齿状顶骨刺:示例病例。
背景:三叉神经痛(TN三叉神经痛(TN)可能是由于神经血管冲突导致三叉神经根入口区受压而引起的,多发于生命的第 6 个 10 年。作者报告了一例三叉神经痛年轻患者的病例,该患者的Meckel洞入口附近有一个鞍顶骨刺,导致三叉神经近端受压:一名 21 岁的女性右侧渐进性 TN 病史长达 5 年。使用不同翻转角度进化磁共振成像(MRI)进行轴向 T2 取样完善并应用优化对比剂后,未发现三叉神经血管受压。然而,矢状面重整显示,沿岩顶有一个突出的骨嵴,导致右侧三叉神经在三叉孔处受到压迫。通过中窝入路切除骨刺后,患者的症状完全缓解:尽管TN最常见的原因是神经血管压迫,但在没有神经血管冲突的情况下,通过磁共振成像检查三叉神经的整个走向以确定神经压迫的其他原因至关重要。骨质压迫是 TN 的一个罕见病因,应予以考虑,尤其是年轻患者。三叉神经沿线是否存在突出的骨性结构可通过矢状位磁共振成像进行可靠评估。https://thejns.org/doi/10.3171/CASE24321。
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