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节段性脊柱发育不良:一名14个月大儿童早期手术干预及结果报告。

Segmental spinal dysgenesis: a report of early surgical intervention and outcome in a 14-month-old child.

作者信息

Morell S M, McCarthy R E, Ocal E

机构信息

Arkansas Childrens Hospital, 1 Children's Way, Little Rock, AR, 72202, USA.

出版信息

Childs Nerv Syst. 2017 Feb;33(2):381-384. doi: 10.1007/s00381-016-3224-x. Epub 2016 Sep 9.

Abstract

Segmental spinal dysgenesis is a rare spinal deformity that is the result of failure of formation resulting in some cases spondyloptosis and neurological dysfunction usually at the thoracolumbar junction. There is little known concerning surgical intervention and timing in these patients. The goal of this case report is to present a case involving 14 months old diagnosed with segmental spinal dysgenesis with stenosis at the thoracolumbar junction soon after birth, treated with definitive posterior spinal fusion and subsequent follow-up.

摘要

节段性脊柱发育不全是一种罕见的脊柱畸形,是由于发育失败导致的,在某些情况下会出现椎体滑脱和神经功能障碍,通常发生在胸腰段交界处。关于这些患者的手术干预和时机,人们了解甚少。本病例报告的目的是介绍一例病例,该病例为一名14个月大的患儿,出生后不久被诊断为节段性脊柱发育不全并伴有胸腰段交界处狭窄,接受了确定性后路脊柱融合术及后续随访。

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