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成功切除一名14个月大儿童的非脊髓分裂性全背侧髓内脂肪瘤。

Successful surgical excision of a nondysraphic holodorsal intramedullary lipoma in a 14-month-old child.

作者信息

Kumar Amandeep, Chandra P S, Bisht Ajay, Garg Ajay, Mahapatra Ashok K, Sharma M C

机构信息

Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Pediatr Neurosurg. 2011;47(4):272-4. doi: 10.1159/000334258. Epub 2012 Feb 22.

Abstract

INTRODUCTION

Nondysraphic intramedullary lipomas of the spinal cord are rare lesions. They are most commonly seen in the second or third decade of life. Their occurrence in the pediatric age group is even rarer.

CASE REPORT

The authors describe a 14-month-old child who presented with delayed motor milestones involving the bilateral lower limbs. The child was unable to sit or stand. MRI revealed a dorsally located intramedullary lipoma extending from C7 to D12. The child underwent C7-L1 laminotomy and gross total excision of the lipoma. Postoperatively, the child improved neurologically and attained normal power in the bilateral lower limbs.

DISCUSSION

Very few cases of extensive intramedullary lipomas involving the dorsal cord have previously been reported. Only two cases of pediatric extensive dorsal lipomas have been mentioned to date. The authors describe successful surgical excision of a holodorsal intramedullary lipoma in a 14-month-old child. To the best of the authors' knowledge, this is the first case being reported of a holodorsal intramedullary lipoma in the youngest patient.

摘要

引言

脊髓非脊髓纵裂性髓内脂肪瘤是罕见病变。它们最常见于生命的第二个或第三个十年。它们在儿童年龄组中的发生更为罕见。

病例报告

作者描述了一名14个月大的儿童,其出现涉及双侧下肢的运动发育迟缓。该儿童无法坐立或站立。磁共振成像(MRI)显示一个位于背侧的髓内脂肪瘤,从C7延伸至D12。该儿童接受了C7 - L1椎板切开术及脂肪瘤全切术。术后,该儿童神经功能改善,双侧下肢获得正常肌力。

讨论

此前很少有关于累及脊髓背侧的广泛髓内脂肪瘤的病例报道。迄今为止,仅提及两例儿童广泛背侧脂肪瘤。作者描述了在一名14个月大的儿童中成功手术切除全背侧髓内脂肪瘤。据作者所知,这是报道的最年轻患者的全背侧髓内脂肪瘤的首例病例。

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