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脊髓纵裂畸形:第二部分:临床综合征。

Split cord malformation: Part II: Clinical syndrome.

作者信息

Pang D

机构信息

Pediatric Neurosurgery, Children's Hospital of Pittsburgh, Pennsylvania.

出版信息

Neurosurgery. 1992 Sep;31(3):481-500. doi: 10.1227/00006123-199209000-00011.

Abstract

Thirty-nine patients with split cord malformations (SCM) were studied in detail with respect to their clinical, radiographic, and surgical findings as well as their outcome data. Eight patients were adults and 31 patients were children. According to the classification endorsed by Part I of the SCM study, 19 patients had Type I SCM (6 adults and 13 children), 18 patients had Type II SCM (2 adults and 16 children), and 2 patients had composite SCM with both lesion types situated in tandem. Six SCMs were cervical, 2 were thoracic, and 31 were in the lumbar region. All 8 adults had pain and progressive sensorimotor deficits at diagnosis. Only 16 of the 31 children had symptoms, and among these, 14 had progressive sensorimotor deficits, but only 6 had pain. The difference in the clinical picture between adults and children is similar to that described in the tethered cord syndrome, except for left-right functional discrepancy, which was prominent in 8 children with SCM but rarely seen in tethered cord syndrome due to other causes. Cutaneous manifestations of either occult or open dysraphic states were present in all but 3 patients; hypertrichosis was by far the best predictor of an underlying SCM, being found in 56% in the series. Neurological deterioration in SCM was independent of the lesion type: the Type I:Type II ratio for symptomatic progression was 13:11. It was also independent of the location of the lesion: 67% of patients with cervical SCMs had symptomatic progression versus 64% of patients with thoracolumbar lesions. High-resolution, thin cut, axial computed tomographic myelography using bone algorithms was more sensitive than magnetic resonance imaging in defining the anatomical details of the SCM. Radiographic classifications of the SCM, using the nature of the median septum and the number of dural tubes as criteria, was always possible without ambiguity. However, whereas every Type I bone septum was identified preoperatively, only 5 Type II fibrous septa were revealed by preoperative imaging, even though a fibrous septum and/or other fibroneurovascular bands were found tethering the hemicords in every Type II case at surgery. Complete imaging studies also showed that all lumbar SCMs had low-lying coni and at least one additional tethering lesion besides the split cords, whereas only 1 of 7 cervical and high thoracic SCMs had a low conus and a second tethering lesion. The surgical goal for SCM was release of the tethered hemicords by eliminating the bone spurs, dural sleeves, fibrous septa, or any fibroneurovascular bands (myelomeningoceles manqué) that might be transfixing the split cord. Type I cases were technically more difficult and had a slightly higher surgical morbidity than Type II cases, especially if an oblique bone septum had asymmetrically divided the cord into one larger hemicord and one smaller, hence, very delicate, hemicord.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对39例脊髓纵裂畸形(SCM)患者的临床、影像学、手术发现及预后数据进行了详细研究。8例为成人,31例为儿童。根据SCM研究第一部分认可的分类,19例患者为I型SCM(6例成人和13例儿童),18例患者为II型SCM(2例成人和16例儿童),2例患者为复合型SCM,两种病变类型串联存在。6例SCM位于颈部,2例位于胸部,31例位于腰部。所有8例成人在诊断时均有疼痛和进行性感觉运动功能障碍。31例儿童中只有16例有症状,其中14例有进行性感觉运动功能障碍,但只有6例有疼痛。成人和儿童临床表现的差异与脊髓栓系综合征中描述的相似,但左右功能差异除外,这种差异在8例SCM儿童中很突出,而在其他原因导致的脊髓栓系综合征中很少见。除3例患者外,所有患者均有隐匿性或开放性脊柱裂状态的皮肤表现;多毛症是潜在SCM的最佳预测指标,在该系列中占56%。SCM的神经功能恶化与病变类型无关:症状进展的I型与II型比例为13:11。它也与病变位置无关:67%的颈部SCM患者有症状进展,而胸腰段病变患者为64%。使用骨算法的高分辨率、薄层轴向计算机断层脊髓造影在确定SCM的解剖细节方面比磁共振成像更敏感。根据中隔的性质和硬膜管的数量对SCM进行影像学分类总是可行且明确的。然而,尽管术前识别了每一例I型骨隔,但术前影像学仅显示了5例II型纤维隔,尽管在每例II型病例的手术中都发现有纤维隔和/或其他纤维神经血管束束缚着半脊髓。完整的影像学研究还显示,所有腰部SCM均有低位圆锥,除脊髓纵裂外至少还有一个额外的束缚病变,而7例颈部和高位胸部SCM中只有1例有低位圆锥和第二个束缚病变。SCM的手术目标是通过消除可能穿透脊髓纵裂的骨赘、硬膜袖、纤维隔或任何纤维神经血管束(隐性脊髓脊膜膨出)来松解束缚的半脊髓。I型病例在技术上更困难,手术发病率略高于II型病例,特别是如果斜行骨隔不对称地将脊髓分为一个较大的半脊髓和一个较小的、因此非常脆弱的半脊髓。(摘要截于400字)

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