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内镜辅助下后颅窝内胚层囊肿切除术:二维手术视频。

Resection of a Posterior Fossa Endodermal Cyst With Exoscopic Assistance: 2-Dimensional Operative Video.

机构信息

Department of Neurosurgery, Lenox Hill Hospital, Zucker School of Medicine at Hofstra/Northwell, New York, New York.

Department of Psychology, The Graduate Center, City University of New York, New York, New York.

出版信息

Oper Neurosurg (Hagerstown). 2020 May 1;18(5):E173-E174. doi: 10.1093/ons/opz238.

Abstract

Neurenteric cysts are rare benign congenital tumors of endodermal origin that most commonly occur in the cervical and upper thoracic spine, with only about 10% to 18% of the reported cases occurring intracranially.1 A definitive preoperative diagnosis is complicated by the variable appearance of neurenteric cysts on magnetic resonance (MR) imaging.2 The recommended treatment of neurenteric cysts is complete surgical resection when possible.3,4 We present a case of a posterior fossa neurenteric cyst. A 33-yr-old man without medical history presented with left-sided headache and mild left-sided facial numbness and weakness. Admission MR imaging revealed a nonenhancing mass, which was hyperintense on T1-weighted MR images, compressing the brainstem anteriorly. The lesion was isointense on T2 FLAIR images and hypointense on diffusion-weighted imaging, initially read as possible epidermoid cyst. The patient underwent a left-sided retrosigmoid craniotomy via far lateral transcondylar approach. The tumor was adjacent to both vertebral arteries, the left PICA, and cranial nerves (CN) VII-XII with superior extension to CN V. The cyst was encased in a thin capsule, and its contents were yellowish in color and ranged from thick liquid to colloidal and caseous consistency. The cyst also contained heavily calcified portions, which were excised using sharp dissection. Images of the cyst wall show that it is focally lined with ciliated columnar epithelium with intracellular mucin confirming an endodermal or neurenteric cyst. After the operation, the patient's symptoms resolved, and he was discharged on postoperative day 4. Postoperative MR images confirmed gross total resection. The patient consented to video production.

摘要

神经肠源性囊肿是一种罕见的良性先天性内胚层起源肿瘤,最常发生于颈段和胸上段脊柱,仅有约 10%~18%的报道病例发生于颅内。1 由于神经肠源性囊肿在磁共振成像(MR)上的表现多变,因此明确的术前诊断较为复杂。2 当可能时,神经肠源性囊肿的推荐治疗方法是完全手术切除。3,4 我们报告了 1 例后颅窝神经肠源性囊肿。1 名 33 岁的男性,无病史,表现为左侧头痛和轻度左侧面部麻木和无力。入院时的 MR 成像显示为无强化肿块,在 T1 加权 MR 图像上呈高信号,向前压迫脑干。病变在 T2 FLAIR 图像上呈等信号,在弥散加权成像上呈低信号,最初读为可能的表皮样囊肿。患者接受了左侧乙状窦后经远外侧经髁突入路开颅手术。肿瘤毗邻双侧椎动脉、左侧小脑后下动脉(PICA)和颅神经(CN)VII-XII,向上延伸至 CN V。囊肿被一层薄囊包裹,内容物呈黄色,从浓稠液体到胶状和干酪样。囊肿还含有大量钙化部分,使用锐性分离切除。囊肿壁的图像显示,其局灶性内衬纤毛柱状上皮,细胞内有黏蛋白,证实为内胚层或神经肠源性囊肿。手术后,患者的症状缓解,于术后第 4 天出院。术后 MR 图像证实大体全切除。患者同意制作视频。

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