老年性腰椎间盘突出伴神经根病2例报告

A. Rahimizadeh, Gholam Housain Shahriyari, E. Abbasnejad, Shaghayegh Rahimizadeh, V. Hassani
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引用次数: 0

摘要

尿酸是一种罕见的遗传性疾病,由酶均质酸二氧化酶(HGA)缺乏引起。这种缺乏导致HGA及其产物作为赭色色素沉积在大关节、椎间盘、皮肤和大动脉内。椎间盘的损害主要发生在胸椎和腰椎,最终逐步导致退变、钙化、假性椎体阻塞和强直性。极少数情况下,受影响的腰椎间盘可能会突出到椎管中,在其钙化之前引起神经根病。在这里,我们介绍了两名女性,她们的急性左下肢神经根病的神经放射学评估显示,在这两种情况下,L4-L5椎间盘突出。这些患者的椎间盘突出与胸椎和上腰椎间盘的钙化有关,与衰老相一致。在去除色素盘材料后,两名患者均表现出明显的恢复。通过对文献的仔细回顾,我们发现除了我们的病例外,只有19例病例以前发表过
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ochronotic Lumbar Disc Herniation with Radiculopathy: Report of Two Cases
Alkaptonuria is a rare genetic disorder caused by deficiency of the enzyme homogentisic acid dioxidase (HGA). This deficiency leads to deposition of HGA and its products as an ochre-colored pigment in the large joints, intervertebral discs, skin, and within major arteries. Affection of the intervertebral discs mostly occurs at the thoracic and lumbar regions which ultimately results in degeneration, calcification, pseudo-blocked vertebra, and ankyloses in a stepwise manner. Rarely, an affected lumbar disc might herniate into the canal and cause radiculopathy before its calcification. Herein we present two women in whom neuroradiological evaluation of an acute left lower limb radiculopathy revealed a sequestrated L4-L5 disc herniation in both cases. Disc prolapse in these patients was associated with calcification of the thoracic and the upper lumbar intervertebral discs, compatible with ochronosis. Following removal of the pigmented disc material, both patients exhibited marked recovery. With careful review of the literature, we found that besides our cases, only 19 cases have been published previously
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