成人拉森综合征伴寰枢关节脱位后凸畸形1例。

IF 1.3
Sushanta K Sahoo, Arsikere N Deepak, Pravin Salunke
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引用次数: 8

摘要

后凸畸形常见于拉森综合征。然而,它在成人中的进展尚不清楚。这些患者的临近节段压迫增加了需要手术的节段的难度。56岁男性,以颈部疼痛和痉挛性四肢瘫痪为主诉。放射学显示后凸畸形(Larsen综合征后遗症)伴寰枢关节脱位。脊髓受压在两个节段都很明显,但仔细评估显示C1-2节段受压和后凸畸形以下部分受压。后凸脊柱已经融合,椎管直径足够。相邻的C1-2节段融合后,病情明显好转。长期的后凸畸形可能不需要矫正,因为它不太可能发展,因为它倾向于自然融合。相反,相邻的水平可能会压缩脊髓由于过度的压力。适当的临床病史和彻底的放射学检查有助于外科医生做出适当的决定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Atlantoaxial dislocation adjacent to kyphotic deformity in a case of adult Larsen syndrome.

Atlantoaxial dislocation adjacent to kyphotic deformity in a case of adult Larsen syndrome.

Kyphotic deformity is often seen in Larsen syndrome. However, its progress in adults is not clear. The adjacent level compression in these patients adds to the difficulty regarding the level that needs to be operated. A 56-year-old male presented with neck pain and spastic quadriplegia. Radiology showed kyphotic deformity (sequelae of Larsen syndrome) with atlantoaxial dislocation. Cord compression was apparent at both levels but careful evaluation showed C1-2 level compression and some compression below the kyphotic deformity. The kyphotic spine was already fused and the canal diameter was adequate. The adjacent level C1-2 was fused and he improved dramatically. Correction of long-standing kyphotic deformity may not be necessary, as it unlikely to progress because of its tendency to fuse naturally. Rather, the adjacent levels are likely to compress the cord due to excessive stress. A proper clinical history and a thorough radiological examination help the surgeon to make an appropriate decision.

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