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伴有全脊髓空洞症的Chiari I畸形的治疗

Management of Chiari I malformations with holocord syringohydromyelia.

作者信息

Feldstein N A, Choudhri T F

机构信息

Department of Neurological Surgery, The Neurological Institute of New York, Columbia University College of Physicians and Surgeons, New York 10032, USA.

出版信息

Pediatr Neurosurg. 1999 Sep;31(3):143-9. doi: 10.1159/000028850.

Abstract

The management of patients with Type I Chiari malformations (CM 1) with or without syringohydromyelia (SHM) has remained quite controversial, and many different surgical procedures have been advocated. Over the past several years, the authors have treated 7 children presenting with CM 1 and holocord syringohydromyelia with suboccipital decompression and duraplasty alone without intradural procedures. All children received MRI imaging at 2-4 months and 1 year postoperatively. On the early postoperative MRI examination, marked reduction in the syringohydromyelia was seen in 6 children, with minimal change in syrinx size in 1 child who was clinically improving after the operation. At 1 year, all children with early collapse remained collapsed, and the child with minimal early collapse demonstrated an approximately 50% reduction in syrinx size. Clinical follow-up (mean 30 months, range 21-50 months) showed good results in all patients: none of the children have required further neurosurgical intervention, and all have shown improvement in their preoperative function. One child with a 46 degrees scoliosis had a complete collapse of her SHM, but ultimately required spinal fusion. The presenting clinical findings, operative technique, MRI imaging and clinical outcomes will be discussed. The results from these 7 patients with CM 1 and holocord syringomyelia suggest that posterior fossa decompression alone (without intradural procedures) can provide excellent radiographic and clinical outcome.

摘要

I型Chiari畸形(CM 1)伴或不伴脊髓空洞症(SHM)患者的治疗一直存在很大争议,人们提倡多种不同的手术方法。在过去几年中,作者对7例患有CM 1和全脊髓空洞症的儿童仅采用枕下减压和硬脑膜成形术进行治疗,未进行硬脊膜内手术。所有儿童在术后2 - 4个月和1年接受了MRI检查。在术后早期的MRI检查中,6例儿童的脊髓空洞症明显缩小,1例临床症状术后改善但空洞大小变化极小的儿童也是如此。1年后,所有早期空洞缩小的儿童空洞仍保持缩小状态,早期空洞缩小极小的儿童空洞大小缩小了约50%。临床随访(平均30个月,范围21 - 50个月)显示所有患者效果良好:所有儿童均无需进一步的神经外科干预,且术前功能均有改善。1例患有46度脊柱侧弯的儿童脊髓空洞症完全消失,但最终需要进行脊柱融合术。将讨论其临床表现、手术技术、MRI成像及临床结果。这7例CM 1和全脊髓空洞症患者的结果表明,单纯后颅窝减压(不进行硬脊膜内手术)可提供良好的影像学和临床效果。

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