Symptomatic spinal metastasis of a supratentorial glioblastoma in a pediatric patient: a case report and comprehensive review of the literature

IF 1.5 4区 医学 Q4 CLINICAL NEUROLOGY Neurochirurgie Pub Date : 2024-07-22 DOI:10.1016/j.neuchi.2024.101583
Uriel Tagle-Vega , Javier G. Patiño-Gómez , Nadin J. Abdalá-Vargas , Paula A. Pulido Bayona , Edgar G. Ordoñez-Rubiano
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Abstract

Spinal metastasis of Glioblastoma is a rare occurrence, especially in pediatric patients, and extremely rare to become symptomatic. The pathology is poorly understood and remains with unclear dissemination mechanisms. The treatment approaches are varied and multimodal therapy (surgery, chemotherapy, and radiotherapy) can be employed to manage this type of metastasis. We report a case of a 17-year-old female who underwent a gross-total resection of a right frontal glioblastoma and had adjuvant therapy with chemo- and radiotherapy. In the sixth month of follow-up, the patient presented a paraparesis, and a distant recurrence at T7-T8 was detected. The patient was treated with gross-total resection of the tumor through a laminectomy. The histopathological results were consistent with an isocitrate dehydrogenase (IDH) wildtype GBM metastasis. The patient was treated with multimodal therapy, including surgery, radiotherapy, and chemotherapy. A complementary comprehensive review of current available literature on this topic is also presented.

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小儿脑室上胶质母细胞瘤的症状性脊柱转移:病例报告和文献综述。
胶质母细胞瘤的脊柱转移非常罕见,尤其是在儿童患者中,而且极少出现症状。人们对其病理机制了解甚少,传播机制也不明确。治疗方法多种多样,可采用多模式疗法(手术、化疗和放疗)来治疗这种转移瘤。我们报告了一例 17 岁女性患者的病例,她接受了右额叶胶质母细胞瘤的大体全切除术,并接受了化疗和放疗的辅助治疗。在随访的第六个月,患者出现偏瘫,并在 T7-T8 位置发现远处复发。患者接受了椎板切除术,对肿瘤进行了全切除。组织病理学结果与异柠檬酸脱氢酶(IDH)野生型 GBM 转移一致。患者接受了包括手术、放疗和化疗在内的多模式治疗。本文还对目前有关该主题的文献进行了全面的补充综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurochirurgie
Neurochirurgie 医学-临床神经学
CiteScore
2.70
自引率
6.20%
发文量
100
审稿时长
29 days
期刊介绍: Neurochirurgie publishes articles on treatment, teaching and research, neurosurgery training and the professional aspects of our discipline, and also the history and progress of neurosurgery. It focuses on pathologies of the head, spine and central and peripheral nervous systems and their vascularization. All aspects of the specialty are dealt with: trauma, tumor, degenerative disease, infection, vascular pathology, and radiosurgery, and pediatrics. Transversal studies are also welcome: neuroanatomy, neurophysiology, neurology, neuropediatrics, psychiatry, neuropsychology, physical medicine and neurologic rehabilitation, neuro-anesthesia, neurologic intensive care, neuroradiology, functional exploration, neuropathology, neuro-ophthalmology, otoneurology, maxillofacial surgery, neuro-endocrinology and spine surgery. Technical and methodological aspects are also taken onboard: diagnostic and therapeutic techniques, methods for assessing results, epidemiology, surgical, interventional and radiological techniques, simulations and pathophysiological hypotheses, and educational tools. The editorial board may refuse submissions that fail to meet the journal''s aims and scope; such studies will not be peer-reviewed, and the editor in chief will promptly inform the corresponding author, so as not to delay submission to a more suitable journal. With a view to attracting an international audience of both readers and writers, Neurochirurgie especially welcomes articles in English, and gives priority to original studies. Other kinds of article - reviews, case reports, technical notes and meta-analyses - are equally published. Every year, a special edition is dedicated to the topic selected by the French Society of Neurosurgery for its annual report.
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