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无神经纤维瘤病患者发生的滑车神经鞘瘤:病例报告及文献复习

Trochlear nerve schwannomas occurring in patients without neurofibromatosis: case report and review of the literature.

作者信息

Santoreneos S, Hanieh A, Jorgensen R E

机构信息

Department of Surgery, Queen Elizabeth Hospital, Adelaide, Australia.

出版信息

Neurosurgery. 1997 Jul;41(1):282-7. doi: 10.1097/00006123-199707000-00050.

DOI:10.1097/00006123-199707000-00050
PMID:9218320
Abstract

OBJECTIVE AND IMPORTANCE

Despite their predilection for sensory nerves, intracranial schwannomas have been reported in a number of mixed and purely motor cranial nerves, especially in association with Type 2 neurofibromatosis. We report the rare occurrence of a trochlear nerve schwannoma in a patient without neurofibromatosis and review 17 other case reports from the literature.

CLINICAL PRESENTATION

A 35-year-old woman presented with an 8-week history of evolving left hemiparesis, bilateral bulbar paresis, and out-of-character emotional lability.

INTERVENTION

She underwent a left temporal craniotomy and a subtemporal, transtentorial approach to the tentorial hiatus, with complete excision of a cisternal trochlear nerve schwannoma.

CONCLUSION

Postoperative complications included temporary oculomotor and abducens nerve palsies and temporary right hemiparesis and mild expressive dysphasia, which were resolved at 23-month follow-up. Preoperative symptoms and signs completely resolved, but a postoperative complete trochlear nerve palsy required inferior oblique myectomy for correction of diplopia. A review of the literature showed no preoperative trochlear nerve involvement in at least 45% of cases. The tumor is isointense on T1- and T2-weighted magnetic resonance images and enhances brightly with gadolinium. The most frequently used approach for surgical excision is the subtemporal approach, and the tumor is almost always totally excised. Long-term follow-up suggests recovery of preoperative deficit, and persisting or new trochlear nerve palsy is the rule.

摘要

目的与重要性

尽管颅内神经鞘瘤好发于感觉神经,但也有报道称其可发生于多条混合性及纯运动性颅神经,尤其是与2型神经纤维瘤病相关时。我们报告1例无神经纤维瘤病患者发生滑车神经鞘瘤的罕见病例,并复习文献中的其他17例病例报告。

临床表现

一名35岁女性,有8周逐渐进展的左侧偏瘫、双侧延髓麻痹及性格改变后的情绪不稳定病史。

干预措施

她接受了左侧颞部开颅手术,并采用颞下经小脑幕入路至小脑幕裂孔,完整切除了脑池内的滑车神经鞘瘤。

结论

术后并发症包括暂时性动眼神经和外展神经麻痹、暂时性右侧偏瘫及轻度表达性失语,在23个月的随访中均已缓解。术前症状和体征完全消失,但术后出现完全性滑车神经麻痹,需要行下斜肌切除术以矫正复视。文献复习显示,至少45%的病例术前滑车神经未受累。该肿瘤在T1加权和T2加权磁共振图像上呈等信号,钆增强后明显强化。手术切除最常用的入路是颞下入路,肿瘤几乎总是能完全切除。长期随访提示术前功能缺损可恢复,持续性或新发滑车神经麻痹较为常见。

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Trochlear nerve schwannomas occurring in patients without neurofibromatosis: case report and review of the literature.无神经纤维瘤病患者发生的滑车神经鞘瘤:病例报告及文献复习
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