首页> 外文期刊>European spine journal: official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society >Expert's comment concerning Grand Rounds case entitled 'Syringomyelia with irreducible atlantoaxial dislocation, basilar invagination and Chiari I malformation' (by Shenglin Wang, Chao Wang, Ming Yan, Haitao Zhou, Liang Jiang).
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Expert's comment concerning Grand Rounds case entitled 'Syringomyelia with irreducible atlantoaxial dislocation, basilar invagination and Chiari I malformation' (by Shenglin Wang, Chao Wang, Ming Yan, Haitao Zhou, Liang Jiang).

机译:关于“ Ground Rounds”案的专家评论,题为“患有不可减少的寰枢椎脱位,基底神经内陷和Chiari I畸形的脊髓空洞症”(王胜林,王超,明燕,周海涛,梁江)。

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摘要

The authors describe a case of a 27-year-old woman with a 5-year history of progressive quadriparesis caused by gradual decompensation of cranio-vertebral junction (CVJ) anomaly. The bone anomalies—assimilation of atlas, syn-ostosis of C2-3 and most probably also platybasia were complicated by anterior atlanto-axial dislocation (AAD) and basilar invagination (BI) concomitantly with Chiari I malformation and cervical syringomyelia. Due to lack of movement on dynamic flexion-extension films and no evidence of reduction after 10 min of traction under general anesthesia, the AAD was considered irreducible (IAAD) as described by Wang et al. [9].
机译:作者描述了一例27岁的妇女,该病因颅椎交界处(CVJ)逐渐失代偿而导致进行性四肢瘫痪5年。骨异常(图集的同化,C2-3的顺行造口以及最可能还有鸭嘴兽)并发前寰枢椎脱位(AAD)和基底内陷(BI),并伴有Chiari I畸形和颈椎细支症。由于在动态屈伸薄膜上缺乏运动,并且在全身麻醉下牵引10分钟后没有证据显示其减少,因此,如Wang等人所述,AAD被认为是不可还原的(IAAD)。 [9]。

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