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先天性腰骶椎椎弓根发育不全或缺如作为儿童年龄组腰椎滑脱的罕见原因。

Congenital hypoplasia or aplasia of the lumbosacral pedicle as an unusual cause of spondylolisthesis in the pediatric age group.

作者信息

Patel Akash J, Vadivelu Sudhakar, Desai Sohum K, Jea Andrew

机构信息

Paul Randall Harrington Neuro-Spine Program, Division of Pediatric Neurosurgery, Texas Children's Hospital, Houston, TX 77030, USA.

出版信息

J Neurosurg Pediatr. 2013 Jun;11(6):717-21. doi: 10.3171/2013.3.PEDS12579. Epub 2013 Apr 19.

Abstract

The authors describe rare cases of congenital hypoplasia of the L-5 pedicles and the congenital absence of the left S-1 pedicle in 2 young girls, respectively, including the presentation, diagnosis, and treatment. Moreover, they review the literature on this clinical entity. The patients presented with intractable chronic low-back pain. Plain radiographs and 2D CT scanning revealed the presence of the aforementioned anomalies. Degenerative changes to adjacent level and contralateral facet joints were thought to be the result of overload and instability and seemed to have led to spondylolisthesis, micromotion at L-5 and S-1, and subsequent low-back pain. The pediatric patients were treated with posterior instrumented fusion with good functional outcomes at a minimum 3-month follow-up. To the best of the authors' knowledge, these are the first reports of intractable low-back pain and spondylolisthesis accompanied by hypoplastic-aplastic pedicles at the lumbosacral junction in children.

摘要

作者分别描述了2名年轻女孩中罕见的L5椎弓根先天性发育不全和左侧S1椎弓根先天性缺如的病例,包括临床表现、诊断和治疗。此外,他们还回顾了关于这一临床实体的文献。患者表现为顽固性慢性下腰痛。X线平片和二维CT扫描显示存在上述异常。相邻节段和对侧小关节的退变被认为是负荷过重和不稳定的结果,似乎导致了椎体滑脱、L5和S1的微动以及随后的下腰痛。这些儿科患者接受了后路器械融合治疗,在至少3个月的随访中取得了良好的功能结果。据作者所知,这些是儿童腰骶部交界处伴有发育不全-发育不全椎弓根的顽固性下腰痛和椎体滑脱的首次报道。

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