Suppr超能文献

马尾神经丛状神经纤维瘤10年随访:一例报告

Plexiform neurofibroma of the cauda equina with follow-up of 10 years: A case report.

作者信息

Chomanskis Zilvinas, Juskys Raimondas, Cepkus Saulius, Dulko Justyna, Hendrixson Vaiva, Ruksenas Osvaldas, Rocka Saulius

机构信息

Department of Neurology and Neurosurgery, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius 03104, Lithuania.

Anatomy, Histology and Anthropology Department, Vilnius University, Faculty of Medicine, Vilnius 03104, Lithuania.

出版信息

World J Clin Cases. 2022 May 16;10(14):4519-4527. doi: 10.12998/wjcc.v10.i14.4519.

Abstract

BACKGROUND

Plexiform neurofibromas are extremely rarely found in the region of cauda equina and can pose a significant challenge in the diagnostic and management sense. To our knowledge, only 7 cases of cauda equina neurofibromatosis (CENF) have been reported up-to-date.

CASE SUMMARY

We describe a case of a 55-year-old man with a 10 years history of progressive lower extremities weakness and bladder dysfunction. Before presenting, patient was misdiagnosed with idiopathic polyneuropathy. Lumbar spine MRI revealed a tortuous tumorous masses in the cauda equina region, extending through the Th12-L4 vertebrae. The patient underwent Th12-L3 Laminectomy with duraplasty. During the operation, the most enlarged electroneurographically silent nerve root was resected, anticipating inadequate decompression if nerve root was spared. The patient's neurological condition improved post-operatively, but urinary retention became the major complaint. We provide a follow-up period of 10 years. During this time, the patient's condition progressively worsened despite extensive decompression. The consequent MRI scans showed progressive enlargement of cauda equina roots and increasing lumbar stenosis, predominantly affecting L3-L4 segment. During the follow-up 8 years after the operation, the patient complained of worsening lower extremities sensorimotor function and neurogenic claudication. Subsequent MRI revealed lumbar spine stenosis at the level of L3-L4, requiring further decompression. The patient underwent a second surgery involving L4-L5 Laminectomy with duraplasty and L2-L5 transpedicular fixation. The post-operative period was uneventful. Latest follow-up 18 mo after the second surgery revealed substantial improvement in patient's well-being.

CONCLUSION

CENF should be kept in mind during the differential diagnostic work-up for polyneuropathies. Management with an extensive decompression, duraplasty and primary spinal fixation represents a rational approach to achieve a sustained symptomatic improvement and superior overall outcome.

摘要

背景

丛状神经纤维瘤在马尾区域极为罕见,在诊断和治疗方面可能构成重大挑战。据我们所知,迄今为止仅报道了7例马尾神经纤维瘤病(CENF)。

病例摘要

我们描述了一名55岁男性患者,有10年进行性下肢无力和膀胱功能障碍病史。在就诊前,患者被误诊为特发性多发性神经病。腰椎磁共振成像(MRI)显示马尾区域有一个迂曲的肿瘤性肿块,延伸至胸12至腰4椎体。患者接受了胸12至腰3椎板切除术及硬脊膜成形术。手术中,切除了电生理检查显示最大且无电活动的神经根,预计保留神经根减压不充分。患者术后神经状况有所改善,但尿潴留成为主要问题。我们进行了10年的随访。在此期间,尽管进行了广泛减压,患者的病情仍逐渐恶化。随后的MRI扫描显示马尾神经根逐渐增粗,腰椎管狭窄加重,主要累及腰3至腰4节段。在术后8年的随访中,患者抱怨下肢感觉运动功能恶化及神经源性间歇性跛行。随后的MRI显示腰3至腰4水平腰椎管狭窄,需要进一步减压。患者接受了第二次手术,包括腰4至腰5椎板切除术及硬脊膜成形术和腰2至腰5经椎弓根固定术。术后恢复顺利。第二次手术后18个月的最新随访显示患者状况有显著改善。

结论

在多发性神经病的鉴别诊断过程中应考虑CENF。采用广泛减压、硬脊膜成形术和初次脊柱固定的治疗方法是实现持续症状改善和更好总体预后的合理方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c37c/9125283/063807a3619e/WJCC-10-4519-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验