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首页> 外文期刊>The Journal of Bone and Joint Surgery. American Volume >Lumbosacral agenesis: a new classification correlating spinal deformity and ambulatory potential.
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Lumbosacral agenesis: a new classification correlating spinal deformity and ambulatory potential.

机译:腰ac骨发育不全:一种新的分类,将脊柱畸形和活动能力相关。

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摘要

BACKGROUND: Lumbosacral agenesis is a rare congenital anomaly. There is no consensus regarding the optimal orthopaedic management of the spinal anomaly and the concomitant lower-extremity deformities. We propose a method to predict ambulatory potential and to identify patients who will benefit from early operative treatment of the lower-extremity deformities to facilitate walking. METHODS: We reviewed the records and radiographs of eighteen patients with total or partial absence of the lumbar spine and total absence of the sacrum. Thirteen patients (Group I) had lumbosacral agenesis alone, and five patients (Group II) had a concomitant myelomeningocele. Three types of spinal deformity were identified. In Type A, there was either a slight gap between the ilia or the ilia were fused in the midline. One or more lumbar vertebrae were absent. The caudad aspect of the spine articulated with the pelvis in the midline, maintaining its vertical alignment. In Type B, the ilia were fused together, some of the lumbar vertebrae were absent, and the most caudad lumbar vertebra articulated with one of the ilia, with the most caudad aspect of the spine shifted away from the midline. In Type C, there was a total agenesis of the lumbar spine, the ilia were fused together, and there was a visible gap between the most caudad intact thoracic vertebra and the pelvis. RESULTS: In Group I, all seven patients with Type-A deformity were community ambulators and one patient with Type-B was a household ambulator. No other patient in the series was able to walk. Nine patients had cervical spine anomalies, and seven patients had scoliosis. No patient was managed with a spinopelvic fusion. CONCLUSIONS: We believe that all Group-I, Type-A patients should have correction of lower-extremity deformities as they have a very good potential to walk. The other patients should have operations on the lower extremities only if the deformities preclude sitting or wearing shoes or braces. The cervical spine should be examined radiographically for atlantoaxial instability or congenital anomalies.
机译:背景:腰ac骨发育不全是一种罕见的先天性异常。关于脊柱畸形的最佳整形外科治疗以及随之而来的下肢畸形尚无共识。我们提出了一种预测门诊潜力并确定将从下肢畸形的早期手术治疗中受益的患者的方法,以促进步行。方法:我们回顾了18例完全或部分不存在腰椎和total骨完全不存在的患者的记录和X线照片。 13名患者(I组)仅患有腰s骨发育不全,而5名患者(II组)具有伴发性脊髓膜膨出。确定了三种类型的脊柱畸形。在A型中,the骨之间有微小的缝隙,或者the骨在中线融合。缺少一个或多个腰椎。脊柱的弯曲部分与中线的骨盆连接,保持其垂直对齐。在B型中,骨融合在一起,一些腰椎不存在,最硬的腰椎与the骨之一相连,脊椎的最粗硬的侧面从中线移开。在C型中,腰椎完全发育不全,the骨融合在一起,最坚硬的完整胸椎和骨盆之间存在明显的缝隙。结果:在第一组中,所有7例A型畸形患者都是社区步行者,而1例B型患者是家庭步行者。该系列中没有其他患者能够行走。 9例有颈椎异常,7例脊柱侧弯。没有患者接受脊柱盂融合术治疗。结论:我们认为所有I型,A型患者均应纠正下肢畸形,因为他们具有很好的行走潜力。其他患者仅在畸形排除了坐,穿鞋或矫正器的情况下才应在下肢进行手术。放射学检查颈椎是否有寰枢椎不稳或先天性异常。

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