Thalamic Tuberculoma Presenting as Isolated Gait Disturbance Without Systemic or Meningeal Symptoms in a 2-Year-Old Child: A Case Report.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
International Medical Case Reports Journal Pub Date : 2026-09-30 eCollection Date: 2026-01-01 DOI:10.2147/IMCRJ.S628684
Khadija Yasmin, Muhammad Abdullah, Sana Shaik, Minahil Zaheer, Aleena Ihtasham, Hamna Hassan Siddiqui, Saira Shamim, Hudaifa Hassan Salad
{"title":"Thalamic Tuberculoma Presenting as Isolated Gait Disturbance Without Systemic or Meningeal Symptoms in a 2-Year-Old Child: A Case Report.","authors":"Khadija Yasmin, Muhammad Abdullah, Sana Shaik, Minahil Zaheer, Aleena Ihtasham, Hamna Hassan Siddiqui, Saira Shamim, Hudaifa Hassan Salad","doi":"10.2147/IMCRJ.S628684","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Intracranial tuberculoma is an important manifestation of pediatric central nervous system tuberculosis, especially in endemic regions. While seizures and signs of raised intracranial pressure are common presenting features, isolated focal neurological deficits without systemic or meningeal symptoms are rare, resulting in diagnostic delay. We report an unusual case of thalamic tuberculoma presenting primarily with gait disturbance in a young child.</p><p><strong>Case presentation: </strong>A 2-year-old boy from Karachi, Pakistan, presented with inability to walk independently at 20 months age. On neurological examination, he had decreased power involving left side of body. MRI of the brain showed a ring-enhancing lesion in the right thalamus extending into the midbrain with surrounding vasogenic edema. Magnetic resonance spectroscopy (MRS) showed a lipid/lactate peak, which supported an infectious granulomatous etiology; a presumptive diagnosis of tuberculoma was made based on imaging findings and household TB exposure.</p><p><strong>Discussion: </strong>Although intracranial tuberculoma does not always present with systemic manifestations of tuberculosis in children, as observed in the present study, it is also a challenging disease to diagnose in young children due to the atypical presentation. Neuroimaging: Early diagnosis is possible. For deep-seated lesions where operative therapy and surgical treatment are highly risky, conservative management is often effective with anti-tuberculous therapy and adjunctive corticosteroids. Early physiotherapy to achieve functional recovery is very important.</p><p><strong>Conclusion: </strong>The case illustrates the need for consideration of intracranial tuberculoma in an individual neurological impairment case, considering children with isolated neurological deficits, when systemic forms of tuberculosis do not develop, even in the absence of evidence of systemic tuberculosis symptoms and history of direct exposure. Prompt imaging, early diagnosis, and treatment with anti-tuberculous therapy may lead to good outcomes.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"19 ","pages":"628684"},"PeriodicalIF":0.7000,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13634239/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Medical Case Reports Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/IMCRJ.S628684","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Intracranial tuberculoma is an important manifestation of pediatric central nervous system tuberculosis, especially in endemic regions. While seizures and signs of raised intracranial pressure are common presenting features, isolated focal neurological deficits without systemic or meningeal symptoms are rare, resulting in diagnostic delay. We report an unusual case of thalamic tuberculoma presenting primarily with gait disturbance in a young child.

Case presentation: A 2-year-old boy from Karachi, Pakistan, presented with inability to walk independently at 20 months age. On neurological examination, he had decreased power involving left side of body. MRI of the brain showed a ring-enhancing lesion in the right thalamus extending into the midbrain with surrounding vasogenic edema. Magnetic resonance spectroscopy (MRS) showed a lipid/lactate peak, which supported an infectious granulomatous etiology; a presumptive diagnosis of tuberculoma was made based on imaging findings and household TB exposure.

Discussion: Although intracranial tuberculoma does not always present with systemic manifestations of tuberculosis in children, as observed in the present study, it is also a challenging disease to diagnose in young children due to the atypical presentation. Neuroimaging: Early diagnosis is possible. For deep-seated lesions where operative therapy and surgical treatment are highly risky, conservative management is often effective with anti-tuberculous therapy and adjunctive corticosteroids. Early physiotherapy to achieve functional recovery is very important.

Conclusion: The case illustrates the need for consideration of intracranial tuberculoma in an individual neurological impairment case, considering children with isolated neurological deficits, when systemic forms of tuberculosis do not develop, even in the absence of evidence of systemic tuberculosis symptoms and history of direct exposure. Prompt imaging, early diagnosis, and treatment with anti-tuberculous therapy may lead to good outcomes.

2岁儿童丘脑结核瘤表现为孤立的步态障碍,无全身或脑膜症状:1例报告。
前言:颅内结核瘤是小儿中枢神经系统结核的重要表现,尤其在流行地区。虽然癫痫发作和颅内压升高是常见的表现特征,但没有全身性或脑膜症状的孤立局灶性神经功能缺损是罕见的,导致诊断延迟。我们报告一个不寻常的病例丘脑结核瘤主要表现为步态障碍在一个年幼的孩子。病例介绍:一名来自巴基斯坦卡拉奇的2岁男孩,在20个月大时表现为不能独立行走。神经学检查显示,患者左侧身体力量减弱。脑MRI显示右丘脑环形强化病变延伸至中脑,周围有血管源性水肿。磁共振波谱(MRS)显示脂质/乳酸峰值,支持感染性肉芽肿病因;根据影像学表现和家庭结核暴露,推定诊断为结核瘤。讨论:虽然在本研究中观察到,颅内结核瘤在儿童中并不总是表现出结核病的全身表现,但由于其不典型的表现,在幼儿中诊断也是一种具有挑战性的疾病。神经影像学:早期诊断是可能的。对于手术治疗和外科治疗风险很大的深部病变,保守治疗通常通过抗结核治疗和辅助皮质类固醇治疗有效。早期物理治疗以达到功能恢复是非常重要的。结论:该病例说明了在单个神经损伤病例中考虑颅内结核瘤的必要性,考虑到孤立性神经功能缺损的儿童,即使没有系统性结核症状和直接接触史的证据,也没有发生全身性结核。及时成像,早期诊断和抗结核治疗可能导致良好的结果。
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
International Medical Case Reports Journal
International Medical Case Reports Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
1.40
自引率
0.00%
发文量
135
审稿时长
16 weeks
期刊介绍: International Medical Case Reports Journal is an international, peer-reviewed, open access, online journal publishing original case reports from all medical specialties. Submissions should not normally exceed 3,000 words or 4 published pages including figures, diagrams and references. As of 1st April 2019, the International Medical Case Reports Journal will no longer consider meta-analyses for publication.
×
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:604180095
Book学术官方微信
小红书