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首页> 外文期刊>Pediatric neurosurgery >Hypothalamic glioma presenting with seizures. a case report and review of the literature.
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Hypothalamic glioma presenting with seizures. a case report and review of the literature.

机译:下丘脑神经胶质瘤伴癫痫发作。病例报告和文献复习。

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摘要

A rare case of hypothalamic glioma in a 7-year-old boy presenting with seizures and diabetes insipidus is reported. Near total decompression of the hypothalamic glioma was done successfully using subfrontal approach. The patient had a stormy postoperative course due to status epilepticus but went on to make a complete recovery. Postoperative radiotherapy/chemotherapy was not given in view of tumor histology (low grade glioma), patient's age and tumor location. Patient remains symptom and seizure free on antiepileptics at 3-year follow-up. The case is presented in the light of its rarity and the literature is reviewed.
机译:据报道,在一个7岁男孩中出现癫痫和尿崩症的下丘脑神经胶质瘤罕见病例。使用额下方法成功完成了下丘脑神经胶质瘤的几乎完全减压。由于癫痫持续状态,该患者术后风雨如磐,但随后得以完全康复。鉴于肿瘤组织学(低度神经胶质瘤),患者的年龄和肿瘤位置,未进行术后放疗/化学治疗。在3年的随访中,抗癫痫药的患者仍无症状和癫痫发作。该案是根据其稀有性提出的,并复习了文献。

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