首页> 外文期刊>Open Journal of Modern Neurosurgery >Voluminous Cystic Trigeminal Schwannoma: Case Report and Literature Review
【24h】

Voluminous Cystic Trigeminal Schwannoma: Case Report and Literature Review

机译:大量囊性三叉施瓦马诺瘤:案例报告和文献综述

获取原文
       

摘要

Voluminous trigeminal schwannomas are rare, predominantly benign growth encapsulated tumors composed of Schwann cells with controversial surgical treatment. They account for 20% to 40% of all trigeminal schwannomas and share the same imaging findings of neurinomas elsewhere. Surgery remains the treatment of choice for most lesions as long as complete excision is feasible. A 35-year-old house wife complained of a 3-month history of progressive right visual field impairment associated with headaches. Neurological examination revealed a complete cavernous sinus syndrome. CT scanning showed a voluminous cystic mass of the right parasellar compartment extending to the optic nerve and the orbit. A concomitant MRI scan revealed more exquisite anatomical details of the lesion. The patient benefitted from a subsequent CT-angiography (not included) which excluded any vascular abnormalities associated with the tumor. Surgical excision of the tumor was warranted and the patient underwent surgery a few days after admission. A pterional extradural-intradural approach combined with incision of the lateral wall of the parasellar compartment via a standard frontotemporal craniotomy was performed and pathological examination was in favor of a cystic trigeminal schwannoma. Post-operative MRI showed a complete excision of the tumor. A 2-year follow-up yielded persistent right monocular blindness. Given this typical appearance of this lesion indicative of both cisternal and parasellar compartment extension, as well as the level of controversy surrounding surgical treatment of these particular tumors; we sought to report this rare case of a voluminous cystic trigeminal schwannoma and share our humble surgical experience of dealing with these lesions. The patient was informed that non-identifying information from the case would be submitted for publication, and she provided consent.
机译:庞大的三叉施沃马斯是罕见的,主要是患有争议手术治疗的施曼细胞组成的良性生长肿瘤。它们占所有三叉子施沃马马苗的20%至40%,并在其他地方分享了神经蛋白酶的相同成像结果。只要完全切除是可行的,手术仍然是大多数病变的选择。一名35岁的房子妻子抱怨了一个与头痛相关的渐进权威视野损害的3个月历史。神经学检查揭示了一个完整的海绵窦综合征。 CT扫描显示出延伸到视神经和轨道的右寄生室的大量囊肿质量。伴随的MRI扫描显示出损伤的更精致的解剖细节。患者受益于随后的CT血管造影(未包括),其排除了与肿瘤相关的任何血管异常。肿瘤的手术切除有保证,患者在入院后几天接受手术。通过标准额发射术术进行了一种具有标准额发射术术的旁边壁切口切口,并且病理学检查有利于囊性三叉施瓦脉。术后MRI显示出肿瘤的完全切除。 2年的随访产生了持续的良好单手抄语。鉴于这种病变的典型外观,指示剖宫产和帕萨拉尔隔室延伸,以及围绕这些特定肿瘤的外科治疗的争议程度;我们试图报告这种罕见的囊性三叉动物施瓦马瘤并分享我们处理这些病变的谦逊手术经验。患者获悉,将提交案件的非识别信息,以便出版,并提供同意。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号