儿童颅内巨大结核瘤:意料之外的诊断和困难重重的治疗--关于两个病例和文献综述。

Surgical neurology international Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI:10.25259/SNI_327_2024
Mohammed Yassine Haouas, Amine Elkhamouye, Khalid Aadoud, Abdelkouddous Laaidi, Khadija Ibahioin, Said Hilmani, Abdelhakim Lakhdar
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引用次数: 0

摘要

背景:颅内巨大结核瘤是脑实质内罕见的占位性病变,直径大于 2.5 厘米。它们可以模仿胶质瘤、脑膜瘤和转移瘤。在没有组织学证据的情况下,很难诊断这种疾病。结核病(TB)影响所有年龄段的人,但在儿童中是一个主要的健康问题。误诊很常见,因为许多临床和放射学特征都没有特异性:病例 1:一名 4 岁儿童出现颅内高压综合征和勇敢-杰克逊癫痫发作。影像学检查显示左侧颞顶叶病变,钆注射后周围环形强化,并附着于硬脑膜。进行了手术切除,组织学分析证实为肉芽肿结核。一个月后,他因神经功能恶化到急诊科就诊。磁共振成像显示中枢神经系统有播散性结核,脑干有结核瘤。患儿在重症监护室治疗一个月后死亡。病例 2:一名 11 岁男孩因头痛就诊,7 个月来头痛逐渐加重。影像学检查发现他的右额部有一个模仿高级别胶质瘤的过程。患儿接受了肿瘤全切手术。几天后,他出现了结核性粟粒疹,并接受了抗结核治疗:结论:治疗包括抗结核治疗和手术。本文介绍了我们对两名患儿进行手术治疗颅内巨大结核瘤的价值,并回顾了相关文献。我们认为,儿童颅内巨大结核瘤的手术治疗效果良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant intracranial tuberculomas in children: An unexpected diagnosis and difficult management - About two cases and review of the literature.

Background: Giant intracranial tuberculomas are rare space-occupying lesions in the brain parenchyma, with a diameter >2.5 cm. They can mimic gliomas, meningiomas, and metastases. Diagnosis of this disease can be difficult without histological evidence. Tuberculosis (TB) affects people of all ages but is a major health problem among children. Misdiagnosis is common, as many clinical and radiological features are non-specific.

Case description: Case 1: A 4-year-old child presented with intracranial hypertensive syndrome and Brave- Jackson seizures. Imaging showed a left temporoparietal lesion with intense peripheral ring enhancement after gadolinium injection, and attaching to the dura mater. Total surgical excision was performed, and histological analysis confirmed granulomatous TB. A month later, he presented to the emergency department with neurological deterioration. Magnetic resonance imaging revealed disseminated TB of the central nervous system, with tuberculomas in the brain stem. The child died after a month in intensive care. Case 2: An 11-year-old boy presented with a headache that had been progressively worsening for 7 months. Imaging revealed a right frontal process mimicking a high-grade glial tumor. The child underwent surgery with total excision of the tumor. After a few days, he developed tubercular miliaria and was put on anti-bacillary treatment.

Conclusion: Treatment includes antituberculosis therapy combined with surgery. This article describes the value of surgery for giant intracranial tuberculomas in two children under our care, with a review of the literature. We believe that the results of surgery for giant intracranial tuberculomas in children are favorable.

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