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[脊髓空洞症、脊柱侧弯与特发性阿诺德-奇亚里畸形:共同病因]

[Syringomyelia, scoliosis and idiopathic Arnold-Chiari malformations: a common etiology].

作者信息

Royo-Salvador M B

机构信息

Servicio de Neurocirugia, Clinica Tres Torres, Barcelona.

出版信息

Rev Neurol. 1996 Aug;24(132):937-59.

PMID:8755356
Abstract

INTRODUCTION

The major theories of the pathogenesis of idiopathic syringomyelia (SMI), idiopathic scoliosis (ESCID) and the Arnold-Chiari malformation (ARCH) are reviewed. A new theory involving a common pathology for SMI, ESCID and ARCH is proposed. Its confirmation depends on the presence of an abnormally low position of the conus medullaris (CM) in patients with SMI. Material and method. Of 292 patients with syringomyelia (SM), 231 patients with SMI were selected, and 55 of these were chosen in whom the level of the conus medullaris (NCM) could be determined, together with figures for SMI, ESCID and ARCH by magnetic resonance (RM). The position of the conus medullaris in 50 patients who did not have SM, ESCID nor ARCH on cervical and lumbar RM was determined.

RESULTS

96.54% of patients with SMI showed some descent of the cerebellar tonsils. 72.97% of the SMI patients also had ESCID: 74.07% of the patients in whom the conus medullaris was seen had scoliosis and a low position of the conus medullaris. 6% of the control group had a conus medullaris at the level of the body of L1, whilst 84.21% of the patients with SMI had a partial or complete image of the conus medullaris at this level. In these patients, an unusually low position of the conus medullaris was confirmed.

CONCLUSIONS

The unusually low position of the conus medullaris in SMI and its close relationship to ARCH and ESCID make it likely that the same pathogenic mechanism is shared by them all. Abnormal asynchromy of growth of the notochord and the spinal cord gives rise to a distinct disorder which shows as different syndromes.

摘要

引言

对特发性脊髓空洞症(SMI)、特发性脊柱侧凸(ESCID)和阿诺德 - 奇亚里畸形(ARCH)发病机制的主要理论进行了综述。提出了一种涉及SMI、ESCID和ARCH共同病理的新理论。其证实取决于SMI患者中脊髓圆锥(CM)位置异常偏低。材料与方法。在292例脊髓空洞症(SM)患者中,选取231例SMI患者,其中55例可确定脊髓圆锥水平(NCM),并通过磁共振成像(RM)获取SMI、ESCID和ARCH的数据。确定了50例在颈椎和腰椎RM检查中未患SM、ESCID和ARCH的患者的脊髓圆锥位置。

结果

96.54%的SMI患者显示小脑扁桃体有一定程度下降。72.97%的SMI患者同时患有ESCID:在可见脊髓圆锥的患者中,74.07%有脊柱侧凸且脊髓圆锥位置偏低。对照组6%的患者脊髓圆锥位于L1椎体水平,而84.21%的SMI患者在此水平有部分或完整的脊髓圆锥影像。在这些患者中,证实了脊髓圆锥位置异常偏低。

结论

SMI中脊髓圆锥位置异常偏低及其与ARCH和ESCID的密切关系表明它们可能具有相同的致病机制。脊索和脊髓生长的异常不同步导致一种独特的病症,表现为不同的综合征。

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