Suppr超能文献

软骨发育不全中的颈髓压迫

Cervicomedullary compression in achondroplasia.

作者信息

Ryken T C, Menezes A H

机构信息

Division of Neurosurgery, University of Iowa Hospitals and College of Medicine, Iowa City.

出版信息

J Neurosurg. 1994 Jul;81(1):43-8. doi: 10.3171/jns.1994.81.1.0043.

Abstract

Six patients with achondroplasia and symptoms suggestive of cervicomedullary junction compression are reviewed; these included three females and three males, with an average age of 8 years (range 7 months to 30 years). The mean duration of symptoms prior to intervention was 1.9 years. Symptoms included occipitocervical pain, ataxia, incontinence, apnea, and respiratory arrest. Radiological investigations consisted of plain films with flexion and extension views, pluridirectional tomography, thin-section computerized tomography, and magnetic resonance imaging. Typical findings included marked foramen magnum stenosis, ventrolateral cervicomedullary junction compression secondary to central and paramesial basilar invagination, and dorsal cervicomedullary junction compression secondary to ligamentous hypertrophy and invagination of the posterior atlantal arch. All patients underwent posterior fossa decompression and atlantal laminectomy. Surgery consistently revealed marked dorsal and paramesial overgrowth of the rim of the rim of the foramen magnum, with thickening and invagination of the atlantal posterior arch and a dense fibrotic epidural band resulting in dorsal cervicomedullary compression. Intraoperative ultrasonography was used to determine the extent of decompression required. Three patients required duraplasty. Three patients had concurrent hydrocephalus, two of whom had undergone ventriculoperitoneal shunting prior to surgical decompression of the posterior fossa. One patient developed a pseudomeningocele postoperatively, requiring serial lumbar punctures before it resolved. No patient developed craniovertebral instability following decompression. Improvement or resolution of symptoms was noted in all patients, with an average follow-up period of 4.8 years. Thus, cervicomedullary compression in patients with achondroplasia can be successfully treated with dorsal decompression of the craniovertebral junction. Dense epidural fibrotic bands are frequently noted in these cases and must be aggressively released to ensure satisfactory decompression.

摘要

对6例患有软骨发育不全且有颈髓交界处受压症状的患者进行了回顾性研究;其中包括3名女性和3名男性,平均年龄为8岁(范围为7个月至30岁)。干预前症状的平均持续时间为1.9年。症状包括枕颈部疼痛、共济失调、大小便失禁、呼吸暂停和呼吸骤停。影像学检查包括屈伸位平片、多向断层扫描、薄层计算机断层扫描和磁共振成像。典型表现包括明显的枕骨大孔狭窄、中央和近中矢状位基底凹陷继发的腹外侧颈髓交界处受压,以及寰椎后弓韧带肥厚和内陷继发的背侧颈髓交界处受压。所有患者均接受了后颅窝减压和寰椎椎板切除术。手术一致显示枕骨大孔边缘明显的背侧和近中矢状位过度生长,寰椎后弓增厚和内陷,以及致密的纤维化硬膜外带导致背侧颈髓受压。术中超声用于确定所需减压的范围。3例患者需要进行硬脑膜成形术。3例患者并发脑积水,其中2例在进行后颅窝手术减压前已接受脑室腹腔分流术。1例患者术后出现假性脑脊膜膨出,在其消退前需要进行多次腰椎穿刺。减压后没有患者出现颅颈不稳定。所有患者均有症状改善或缓解,平均随访期为4.8年。因此,软骨发育不全患者的颈髓受压可通过颅颈交界处背侧减压成功治疗。在这些病例中经常发现致密的硬膜外纤维化带,必须积极松解以确保满意的减压效果。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验