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脊髓拴系综合征患儿的鲁宾斯坦-泰比综合征

Rubinstein-Taybi syndrome in children with tethered spinal cord.

作者信息

Tanaka Tomoko, Ling Benjamin C, Rubinstein Jack H, Crone Kerry R

机构信息

Department of Neurosurgery, Cincinnati Children's Hospital Medical Center, Ohio, USA.

出版信息

J Neurosurg. 2006 Oct;105(4 Suppl):261-4. doi: 10.3171/ped.2006.105.4.261.

Abstract

OBJECT

The authors identified eight patients with Rubinstein-Taybi syndrome (RTS) and examined how the underlying conditions of this syndrome can impede the detection of symptoms associated with a tethered spinal cord. They also reviewed the literature and did not find any published series describing such an association with this syndrome.

METHODS

In this retrospective review, the authors report the diagnosis, treatment, and outcome of tethered spinal cord in eight children (age range 2-14 years) with RTS. The patients presented between 1995 and 2003 with neurogenic bladder, decreased activity, gait disturbance, and low-back pain. The children were examined using whole-spine magnetic resonance (MR) imaging and, in recent years, their spinal cord movement was assessed using cine MR imaging. After undergoing lumbar laminectomy and spinal cord untethering procedures, six patients experienced improvement in symptoms associated with tethered spinal cord such as pain, urinary tract infection, incontinence, spasticity, and neurogenic bladder.

CONCLUSIONS

Although some underlying conditions of RTS may mask the symptoms of a tethered spinal cord in children, careful attention to the patient's medical history as provided by his or her parents may aid in early diagnosis, evaluation, and treatment, thus preventing further neurological deterioration and leading to improved outcomes.

摘要

目的

作者识别出8例患有鲁宾斯坦-泰比综合征(RTS)的患者,并研究该综合征的潜在病情如何妨碍对与脊髓拴系相关症状的检测。他们还查阅了文献,未发现任何已发表的系列报道描述过该综合征与脊髓拴系的这种关联。

方法

在这项回顾性研究中,作者报告了8例患有RTS的儿童(年龄范围2至14岁)脊髓拴系的诊断、治疗及结果。这些患者于1995年至2003年间出现神经源性膀胱、活动减少、步态障碍及腰痛。对这些儿童进行了全脊柱磁共振(MR)成像检查,近年来还使用电影MR成像评估了他们的脊髓运动情况。在接受腰椎椎板切除术和脊髓松解手术后,6例患者与脊髓拴系相关的症状如疼痛、尿路感染、尿失禁、痉挛及神经源性膀胱等有所改善。

结论

尽管RTS的某些潜在病情可能掩盖儿童脊髓拴系的症状,但仔细关注患儿父母提供的病史可能有助于早期诊断、评估及治疗,从而防止神经功能进一步恶化并改善预后。

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