Iskandar B J, Hedlund G L, Grabb P A, Oakes W J
Division of Pediatric Neurosurgery, Department of Pediatric Imaging, Children'sHospital,Birmingham,Alabama, USA.
J Neurosurg. 1998 Aug;89(2):212-6. doi: 10.3171/jns.1998.89.2.0212.
To provide more information about this rare condition, the authors describe five cases of syringohydromyelia without hindbrain herniation. Preoperative magnetic resonance imaging with and without gadolinium-diethylenetriamine pentaacetic acid revealed no evidence of spinal cord tumor, arachnoiditis, or spinal dysraphism.
Craniocervical decompression was performed in all patients, after which there was resolution of the symptoms in the four symptomatic patients, and all five showed marked reduction in the size of the syrinx.
The authors hypothesize the rare occurrence of syringohydromyelia resulting from a Chiari-like pathophysiological condition but lacking a hindbrain hernia. Patients with this condition may benefit from craniocervical decompression.
为了提供更多关于这种罕见病症的信息,作者描述了5例无后脑疝的脊髓空洞症病例。术前钆喷酸葡胺增强和未增强磁共振成像均未显示脊髓肿瘤、蛛网膜炎或脊柱裂的迹象。
所有患者均接受了颅颈减压手术,术后4例有症状的患者症状得到缓解,所有5例患者的空洞大小均显著缩小。
作者推测无后脑疝的脊髓空洞症罕见,是由类似Chiari的病理生理状况引起的。患有这种病症的患者可能从颅颈减压术中获益。