Midline-Sparing Interapophysealaminar Decompression Technique for Management of Lumbar Stenosis in Pediatric Achondroplasia.

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY
Stacey Podkovik, Kevin N Martins, Hammad Ghanchi, Brian W Hanak
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引用次数: 0

Abstract

Introduction: Achondroplasia is the most common form of short-limb dwarfism in humans, with an incidence of 1 in 25,000-40,000 live births. About one-third of achondroplasia patients will require operative intervention for lumbar spinal stenosis, generally presenting with progressive neurogenic claudication. The anatomy of the achondroplastic lumbar spine, with shortened pedicles, hypertrophic zygapophyseal joints, and thickened laminae frequently results in the development of multilevel interapophyseolaminar stenosis, while stenosis is usually absent at the mid-laminar levels secondary to pseudo-scalloping of the vertebral bodies. Treatment remains controversial, as disrupting the posterior tension band with complete laminectomies in the pediatric population puts patients at risk of developing post-laminectomy kyphosis.

Case presentation: A 15-year-old girl with achondroplasia presented to clinic with debilitating neurogenic claudication in the setting of multilevel lumbar interapophyseolaminar stenosis. We present a technical case report of her successful surgical treatment using a midline posterior tension band sparing modification to the interapophyseolaminar decompression technique proposed by Thomeer et al. [J Neurosurg. 2002;96(3 Suppl l):292-7].

Conclusion: We demonstrate that an adequate interapophyseolaminar decompression can be achieved through the performance of bilateral laminotomies, bilateral medial facetectomies, and undercutting of the ventral spinous process while preserving supraspinous and interspinous ligament attachments. Given the generally multilevel nature of lumbar stenosis and longer life expectancies of pediatric achondroplasia patients, decompressive surgical interventions must aspire to minimize disruption of spine biomechanics if fusion surgery is to be avoided.

保留中线椎间减压技术治疗小儿软骨发育不全腰椎管狭窄。
软骨发育不全是人类最常见的短肢侏儒症,发病率为1 / 25000 - 40000。约三分之一的软骨发育不全患者因腰椎管狭窄需要手术干预,通常表现为进行性神经源性跛行。软骨发育不全腰椎的解剖结构,椎弓根缩短,关节关节肥大,椎板增厚,经常导致多节段椎板间狭窄,而椎体假扇贝后继发的椎板中层通常不存在狭窄。治疗仍然存在争议,因为在儿童人群中,椎板全切除术会破坏后张力带,使患者有椎板切除术后后凸的风险。病例介绍:一个15岁的女孩,软骨发育不全,在多节段腰椎椎间板狭窄的背景下,以衰弱性神经源性跛行来到临床。我们报告了一例成功的手术病例,采用Thomeer等人提出的后路张力带保留改良椎间板减压技术[J]; 2002;96(3增刊1):292-7。结论:我们证明,通过双侧椎板切开术、双侧内侧面切开术和削弱腹侧棘突,同时保留棘上韧带和棘间韧带的附着,可以实现充分的椎间板减压。考虑到腰椎管狭窄通常是多节段性的,儿童软骨发育不全患者的预期寿命更长,如果要避免融合手术,减压手术干预必须尽量减少脊柱生物力学的破坏。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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