Kadri Paulo A S, Al-Mefty Ossama
Department of Neurosurgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Neurosurg Focus. 2004 Aug 15;17(2):E9. doi: 10.3171/foc.2004.17.2.9.
Schwannomas of the jugular foramen are rare, comprising between 2 and 4% of intracranial schwannomas. The authors retrospectively analyzed their surgical experience with schwannomas of the lower cranial nerves that presented with intra- and extracranial extensions through an enlarged jugular foramen. The transcondylar suprajugular approach was used without sacrificing the labyrinth or the integrity of the jugular bulb. In this report the clinical and radiological features are discussed and complications are analyzed.
This retrospective study includes six patients (three women and three men, mean age 31.6 years) with dumbbell-shaped jugular foramen schwannomas that were surgically treated by the senior author during a 5.5-year period. One patient had undergone previous surgery elsewhere. Glossopharyngeal and vagal nerve deficits were the most common signs (appearing in all patients), followed by hypoglossal and accessory nerve deficits (66.6%). Two or more signs or symptoms were present in every patient. Three tumors presented with cystic degeneration. In four patients the jugular bulb was not patent on neuroimaging studies. The suprajugular approach was used in five patients; the origin of the tumor from the 10th cranial nerve could be defined in three of them. All lesions were completely resected. No death or additional postoperative cranial nerve deficits occurred in this series. Aspiration pneumonia developed in one patient. Preoperative deficits of the ninth and 10th cranial nerves improved in one third of the patients and half recovered mobility of the tongue. No recurrence was discovered during the mean follow-up period of 32.8 months.
With careful, extensive preoperative evaluation and appropriate planning of the surgical approach, dumbbell-shaped jugular foramen schwannomas can be radically and safely resected without creating additional neurological deficits. Furthermore, recovery of function in the affected cranial nerves can be expected.
颈静脉孔神经鞘瘤较为罕见,占颅内神经鞘瘤的2%至4%。作者回顾性分析了他们对通过扩大的颈静脉孔出现颅内和颅外延伸的下颅神经神经鞘瘤的手术经验。采用经髁上颈静脉孔入路,未牺牲迷路或颈静脉球的完整性。在本报告中,讨论了临床和放射学特征并分析了并发症。
这项回顾性研究纳入了6例(3名女性和3名男性,平均年龄31.6岁)哑铃形颈静脉孔神经鞘瘤患者,这些患者在5.5年期间由资深作者进行了手术治疗。1例患者曾在其他地方接受过手术。舌咽神经和迷走神经功能障碍是最常见的体征(所有患者均出现),其次是舌下神经和副神经功能障碍(66.6%)。每位患者均有两种或更多的体征或症状。3例肿瘤出现囊性变。4例患者在神经影像学检查中颈静脉球不显影。5例患者采用上颈静脉孔入路;其中3例可明确肿瘤起源于第10颅神经。所有病变均完全切除。本系列中无死亡或术后额外的颅神经功能障碍发生。1例患者发生吸入性肺炎。三分之一的患者术前第9和第10颅神经功能障碍有所改善,一半患者恢复了舌的活动度。在平均32.8个月的随访期内未发现复发。
通过仔细、全面的术前评估和适当的手术入路规划,哑铃形颈静脉孔神经鞘瘤可以在不造成额外神经功能障碍的情况下被彻底、安全地切除。此外,受累颅神经的功能有望恢复。