Suppr超能文献

2岁女童马尾水平硬膜内髓外表皮样囊肿:一例罕见病例报告

Intradural extramedullary epidermoid cyst at cauda equina level in 2-years female child: A rare case report.

作者信息

Aristianti Aristianti, Wiranata Sinta, Wardhana Dewa Putu Wisnu

机构信息

Department of Neurosurgery, Medical Faculty of Hasanuddin University, Makassar 90245, Indonesia.

Faculty of Medicine, Universitas Udayana, Denpasar, Bali 80232, Indonesia.

出版信息

Int J Surg Case Rep. 2025 Feb;127:110986. doi: 10.1016/j.ijscr.2025.110986. Epub 2025 Jan 29.

Abstract

INTRODUCTION

Spinal epidermoid cysts are noncancerous growths that comprise fewer than 1 % of the abnormalities found in the spine. An epidermoid cyst in the intradural extramedullary region, without any associated dysraphism, trauma, or syndromic conditions, and its subsequent successful identification and surgical removal without any adverse effects on the patient, is a highly uncommon event.

CASE PRESENTATION

A 2-year-old female visited the outpatient clinic with a skin fold on the back that has been present since birth, without any abnormalities in the spinal cord or any injuries. The patient had no impairments and was in good condition, displaying satisfactory feeding and playing behavior. An intradural extramedullary lesion indicating the presence of several epidermoid cysts at the L3-L4 level of the cauda equina was identified in the lumbosacral MRI. The patient underwent a surgical procedure called laminectomy and durotomy to remove a tumor. The histological examination confirmed the diagnosis of an epidermoid cyst.

DISCUSSION

Epidermoid cysts are infrequently found in the intradural extramedullary region of the spinal canal. A laminectomy procedure was conducted to excise a tumor in this patient. The patient experienced neurogenic bladder dysfunction following surgery, necessitating a consultation with the urologist. The patient has returned to baseline with no signs of deterioration.

CONCLUSION

Surgery by total removal is the treatment of choice for spinal ECs, providing a disease-free outcome and preventing further neurological deficits.

摘要

引言

脊髓表皮样囊肿是一种非癌性生长物,在脊柱发现的异常中占比不到1%。硬膜内髓外区域出现表皮样囊肿,且无任何相关的神经管闭合不全、创伤或综合征情况,随后成功识别并手术切除且对患者无任何不良影响,这是极为罕见的事件。

病例介绍

一名2岁女性因自出生起背部就有皮肤褶皱前来门诊就诊,脊髓无任何异常且未受过伤。患者无功能障碍,状况良好,进食和玩耍行为令人满意。腰骶部磁共振成像(MRI)显示硬膜内髓外病变,提示在马尾神经L3 - L4水平存在多个表皮样囊肿。患者接受了名为椎板切除术和硬脊膜切开术的手术以切除肿瘤。组织学检查证实为表皮样囊肿。

讨论

表皮样囊肿在椎管的硬膜内髓外区域很少见。对该患者进行了椎板切除术以切除肿瘤。患者术后出现神经源性膀胱功能障碍,需要咨询泌尿科医生。患者已恢复至基线水平,无恶化迹象。

结论

通过完全切除进行手术是脊髓表皮样囊肿的首选治疗方法,可实现无病状态并预防进一步的神经功能缺损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a355/11834098/3fc817797729/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验