高级别胶质瘤在儿童和青年人群中的增加

Peer Asad Aziz, Muhammad Hamid Ali, Sanaullah Pathan, Mubarak Hussain, Suhail Ahmed Aghani, Riaz Ahmed Raja
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引用次数: 0

摘要

背景/目的:胶质母细胞瘤是最常见的原发性脑癌之一。本研究旨在评估青少年和儿童人群中高级别胶质瘤的趋势转变。材料和方法:这是一项描述性和横断面研究;该研究是在利亚奎特医学和健康科学大学神经外科进行的。所有疑似脑肿瘤的病例,不论年龄或性别,均被评估为胶质母细胞瘤。一旦在影像学上确定实体瘤具有胶质母细胞瘤的一致特征,则建立临时诊断。之后,患者接受了脑活检。患者的性别、人口统计学、临床表现、放射学记录等以预先确定的形式收集。结果:22例患者被诊断为胶质母细胞瘤,患者的高发年龄在20 ~ 30岁之间。肿瘤最常见的位置是靠近中线的皮质下。有轻微的男性优势。8例患者在发病时KPS水平< 70,其中2例为婴儿,4例为植物人状态,2例继发于颅内压升高的意识丧失。复发率为27.2%。结论:虽然本研究时间短,随访时间短,随访结果令人惊讶,但由于胶质母细胞瘤患者的趋势可能发生变化,因此需要进一步从不同维度特别是分子水平和遗传学上进行详细的检查,以准确了解疾病,并应进行国家登记和警报,以便及时发现问题,有效应对并制定未来策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increment of High-Grade Gliomas Among Pediatric and Young Adult Population
Background/Objective:  Glioblastomas are among the commonest primary brain cancers. This study aimed to assess the trend shift of high-grade glioma in our setting among the young and pediatric population. Materials and Methods:  This is a descriptive and cross-sectional study; it was carried out at the Department of Neurosurgery, Liaquat University of Medical and Health Sciences, between duration. All cases with suspected brain tumors, irrespective of age or gender were assessed for glioblastoma. Once a solid tumor was identified on imaging with consistent features of glioblastoma, a provisional diagnosis was established. After that, the patient underwent a brain biopsy. Patients' gender, demographics, clinical presentation, radiologic records, etc. were collected in a predefined proforma. Results:  22 patients were diagnosed with glioblastoma with a high frequency of patients between the age range of 20 to 30 years. The most common location of the tumor was subcortical near the midline. There was slight male predominance. 8 patients had levels of KPS at presentation < 70 and among those two were infants, four were in a vegetative state, and two had a loss of consciousness secondary to increased intracranial pressure. The recurrence rate among those who came back for follow-ups was 27.2%. Conclusion:  Though it is a short study with short follow-up results were astonishing due to perhaps trend shift among Glioblastoma patients, a further detailed workup is needed in different dimensions especially molecular level and genetics to know exactly about the disease and the national registry should be carried and alarmed to identify the problem at once, counter effectively and make a future strategy.
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