A Peculiar Concurrent Presentation of Spinal Tuberculosis In A Diagnosed Case of Neurofibromatosis Type 1 – An Atypical Case Report

Vishnu Vikraman Nair, Vishal G. Kundnani, Mukul Jain, Sunil Chodavadiya, Jenil R. Patel
{"title":"A Peculiar Concurrent Presentation of Spinal Tuberculosis In A Diagnosed Case of Neurofibromatosis Type 1 – An Atypical Case Report","authors":"Vishnu Vikraman Nair, Vishal G. Kundnani, Mukul Jain, Sunil Chodavadiya, Jenil R. Patel","doi":"10.26502/fjsrs0057","DOIUrl":null,"url":null,"abstract":"Spinal tuberculosis is a prevalent ailment observed in the Asian demographic, which can result in neurodeficit if not addressed during the initial phases. Neurofibromatosis is a hereditary disorder that results in the manifestation of dystrophic bony characteristics accompanied by the development of multiple spinal tumors. This study presents a unique case of a young female who had previously been diagnosed with Neurofibromatosis. Additionally, she exhibited symptoms of tubercular spondylodiscitis, resulting in kyphotic deformity and paraparesis. The present case report discusses the challenges encountered during the preoperative and intra-operative management of a patient presenting with the co-occurrence of neurofibromatosis and tuberculosis of the spine. Despite the advancements in imaging modalities, such as magnetic resonance imaging, and surgical techniques, the prompt diagnosis and management of spinal tuberculosis with Neurofibramatosis remains complex and demanding. The objective of this review is to examine the diagnosis, preoperative planning, and treatment of spinal tuberculosis in a patient of Neurofibromatosis type 1, utilizing studies that possess adequate literature, lucidly presented outcomes, and defensible conclusions.","PeriodicalId":73951,"journal":{"name":"Journal of spine research and surgery","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of spine research and surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26502/fjsrs0057","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Spinal tuberculosis is a prevalent ailment observed in the Asian demographic, which can result in neurodeficit if not addressed during the initial phases. Neurofibromatosis is a hereditary disorder that results in the manifestation of dystrophic bony characteristics accompanied by the development of multiple spinal tumors. This study presents a unique case of a young female who had previously been diagnosed with Neurofibromatosis. Additionally, she exhibited symptoms of tubercular spondylodiscitis, resulting in kyphotic deformity and paraparesis. The present case report discusses the challenges encountered during the preoperative and intra-operative management of a patient presenting with the co-occurrence of neurofibromatosis and tuberculosis of the spine. Despite the advancements in imaging modalities, such as magnetic resonance imaging, and surgical techniques, the prompt diagnosis and management of spinal tuberculosis with Neurofibramatosis remains complex and demanding. The objective of this review is to examine the diagnosis, preoperative planning, and treatment of spinal tuberculosis in a patient of Neurofibromatosis type 1, utilizing studies that possess adequate literature, lucidly presented outcomes, and defensible conclusions.
1型神经纤维瘤病并发脊柱结核的特殊表现-一个不典型病例报告
脊柱结核是亚洲人口中观察到的一种普遍疾病,如果在最初阶段不加以解决,可能导致神经功能障碍。神经纤维瘤病是一种遗传性疾病,导致骨性营养不良的表现,并伴有多发性脊柱肿瘤的发展。本研究提出了一个独特的情况下,年轻女性谁曾被诊断为神经纤维瘤病。此外,她还表现出结核性脊柱炎的症状,导致后凸畸形和截瘫。本病例报告讨论了在术前和术中遇到的挑战,病人呈现神经纤维瘤病和脊柱结核的共存管理。尽管磁共振成像和手术技术等成像方式取得了进步,但脊柱结核合并神经纤维瘤病的及时诊断和治疗仍然很复杂,而且要求很高。本综述的目的是研究1型神经纤维瘤病患者脊柱结核的诊断、术前计划和治疗,利用具有充分文献、清晰结果和可辩护结论的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信