首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Pediatric brain tumors in Nigeria: Clinical profile, management strategies, and outcome
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Pediatric brain tumors in Nigeria: Clinical profile, management strategies, and outcome

机译:尼日利亚小儿脑肿瘤:临床概况,治疗策略和结果

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Introduction: Although modern neuroimaging has facilitated early care of brain tumors in children worldwide, there are, however, few published reports on clinical profile, treatment, and outcome of brain tumors in children from our subregion. Purpose: We aimed to retrospectively study the clinical profile and outcome of pediatric brain tumors in a tertiary referral center from a developing country. Methods: Forty pediatric patients with histologically verified brain tumors managed by the authors over a 13-year period (May1994-April 2006) were studied. Patients' data from clinical, radiological, and pathology records were analyzed using the statistical package for social sciences version 16. Results: The mean age was 9.75 years (range 1-15 years). Twenty-two males, 18 females. Common presenting symptoms were headaches (23 patients, 57.5 %) and seizures (15 patients, 37.5 %). Hyperreflexia (72.5 %) and focal motor deficits (62.5 %) were the most common neurologic signs. The mean interval from onset of symptoms to neurosurgical diagnosis was 13.4 months (95 % CI). All patients had tumor resection, while 11 (27.5 %) patients received adjuvant radiotherapy. Hydrocephalus occurred in 19 (47.5 %) patients and was associated with early presentation (X2 = 10.65, p 0.01). Low-grade astrocytoma (25 %) and medulloblastoma (25 %) were the most common tumors. Survival at 1 and 5 years were 56 and 47 %, respectively. Conclusion: Focal motor signs and elevated intracranial pressure are the salient presenting features of brain tumors in children seen in Nigeria. Those of them with hydrocephalus are likely to present early. The outcome for pediatric brain tumors remains poor.
机译:简介:尽管现代神经影像技术已促进了全世界儿童脑瘤的早期护理,但是,关于本次地区儿童脑瘤的临床概况,治疗和结局的报道很少。目的:我们旨在回顾性研究来自发展中国家的三级转诊中心的小儿脑肿瘤的临床概况和结局。方法:研究了作者在13年内(1994年5月至2006年4月)治疗的40例经组织学证实为脑肿瘤的儿科患者。使用社会科学版本16的统计软件包对来自临床,放射学和病理学记录的患者数据进行了分析。结果:平均年龄为9.75岁(范围为1-15岁)。男22名,女18名。常见症状为头痛(23例,占57.5%)和癫痫发作(15例,占37.5%)。反射亢进(72.5%)和局灶性运动障碍(62.5%)是最常见的神经系统症状。从症状发作到神经外科诊断的平均间隔为13.4个月(95%CI)。所有患者均进行了肿瘤切除,而11例(27.5%)患者接受了辅助放疗。脑积水发生在19位(47.5%)患者中,并与早期就诊相关(X2 = 10.65,p <0.01)。低度星形细胞瘤(25%)和髓母细胞瘤(25%)是最常见的肿瘤。 1年和5年生存率分别为56%和47%。结论:运动性体征和颅内压升高是尼日利亚儿童脑瘤的主要表现特征。那些患有脑积水的人可能会出现较早。小儿脑肿瘤的预后仍然很差。

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