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椎管内神经肠囊肿的临床表现与手术结果。

Clinical presentation and surgical outcomes of intramedullary neurenteric cysts.

机构信息

Department of Neurosurgery, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital; and.

Department of Neuropathology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

出版信息

J Neurosurg Spine. 2015 Jul;23(1):99-110. doi: 10.3171/2014.11.SPINE14352. Epub 2015 Apr 24.

Abstract

OBJECT

Intramedullary neurenteric cysts (NECs) are exceedingly rare lesions and have been previously reported in case reports. The aim of this study was to determine the clinical manifestations, radiological features, and long-term prognosis of patients with such lesions.

METHODS

The authors retrospectively reviewed the records of 13 patients with an intramedullary NEC. Each patient underwent MRI, laminotomy, and microsurgery. The accurate diagnosis was based on imaging and pathology findings. Each patient's follow-up status was determined through individual office visits and a structured telephone interview.

RESULTS

The series included 7 male and 6 female patients. Progressive or intermittent motor deficit was the main symptom associated with or without pain or sensory disturbance. Five cysts were located in the cervical cord, 1 in the cervicothoracic cord, 3 in the thoracic cord, and 4 in the conus medullaris. Concurrent malformations included scoliosis (3 cases), fusion of rib (1 case), enlarged spinal canal (1 case), tethered spinal cord (1 case), and ectocardia (1 case). Gross-total resection of the cyst was achieved in 8 cases, and subtotal resection (STR) was achieved in 5 cases. All patients were followed up, with a mean duration of 66.5 months. Cyst recurrence was observed in 4 cases after STR. In 2 cases the patients underwent reoperation; the other 2 patients remained clinically stable and did not undergo reoperation. At the last evaluation, neurological function was improved in 11 patients and remained stable in 2 patients.

CONCLUSIONS

Intramedullary NECs should be considered in the differential diagnosis of a middle-aged patient with intermittent neurological symptoms and concurrent malformations. Early surgery is advocated to prevent permanent neurological deficits. When gross-total resection cannot be achieved, maximally safe removal under the protection of intraoperative neuromonitoring is advised. Because of the high risk of cyst recurrence, routine follow-up MRI is needed. If a residual cyst shows obvious regrowth and results in neurological deficits, timely reoperation with a goal of STR should be performed.

摘要

目的

髓内神经肠上皮囊肿(NEC)是非常罕见的病变,此前已有病例报告。本研究旨在确定此类病变患者的临床表现、影像学特征和长期预后。

方法

作者回顾性分析了 13 例髓内 NEC 患者的病历。每位患者均接受 MRI、椎板切除术和显微镜手术。准确的诊断基于影像学和病理学结果。每位患者的随访情况通过个别就诊和结构化电话访谈确定。

结果

该系列包括 7 名男性和 6 名女性患者。进行性或间歇性运动功能障碍是主要症状,伴有或不伴有疼痛或感觉障碍。5 个囊肿位于颈髓,1 个位于颈胸髓,3 个位于胸髓,4 个位于脊髓圆锥。并发畸形包括脊柱侧凸(3 例)、肋骨融合(1 例)、椎管扩大(1 例)、脊髓栓系(1 例)和心外膜(1 例)。8 例患者实现了囊肿的大体全切除,5 例患者实现了次全切除(STR)。所有患者均得到随访,平均随访时间为 66.5 个月。STR 后观察到 4 例囊肿复发。2 例患者再次手术;另外 2 例患者临床稳定,未再次手术。最后评估时,11 例患者的神经功能得到改善,2 例患者保持稳定。

结论

对于间歇性神经症状和并发畸形的中年患者,应考虑髓内 NEC 作为鉴别诊断。提倡早期手术以防止永久性神经功能缺损。当无法实现大体全切除时,建议在术中神经监测保护下尽可能安全地切除。由于囊肿复发风险高,需要常规进行随访 MRI。如果残留囊肿明显增大并导致神经功能缺损,应及时进行以 STR 为目标的再次手术。

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