多形性胶质母细胞瘤巨细胞变异:一罕见儿童变异报告

Zahra Aminparast, M. Ramezani
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引用次数: 0

摘要

恶性神经胶质肿瘤在儿童中很少见。巨细胞变异是一种罕见的胶质母细胞瘤亚型,约占脑肿瘤的0.8%,占胶质母细胞瘤的5%。巨细胞胶质母细胞瘤是一种主要发生于儿童和成人的男性肿瘤。由于这种变异的流行率很低,可用的信息有限。一名11岁女童,主诉为进行性持续性头痛。MRI显示右顶叶有明确的囊性病变,伴实性壁壁成分,对同侧心室系统有压迫作用。手术完成了。在病理学家报告多形性胶质母细胞瘤(一种巨细胞变体)后,患者接受了30次放射治疗。患者18个月后因头痛再次入院,病理证实肿瘤复发。基于放射学,巨细胞胶质母细胞瘤不能与普通亚型胶质母细胞瘤区分开来。病理学家必须意识到这个实体,组织学鉴别诊断是诊断、预后和治疗目的的保证。
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Giant Cell Variant of Glioblastoma Multiforme: Report of a Rare Variant in a Child
Malignant glial tumors are rare in children. Giant cell variant is a rare subtype of glioblastoma, accounting for about 0.8% of brain tumors and 5% of glioblastoma tumors. Giant cell glioblastoma is a male predominant tumor in children and adults. Due to the low prevalence of this variant, available information is limited. An 11-year-old female child was referred with a chief complaint of a progressive persistent headache. MRI showed a well-defined cystic lesion with a solid mural component in the right parietal lobe with a compression effect on the ipsilateral ventricular system. Surgery was done. After the pathologist reported glioblastoma multiforme, a giant cell variant, the patient received 30 sessions of radiation therapy. The patient was readmitted 18 months later with a headache, and the pathologist confirmed the recurrence of the tumor. Based on radiology, the giant cell glioblastoma cannot be distinguished from the common subtype glioblastoma. The pathologists must be aware of this entity, and histologic differential diagnoses are warranted for diagnostic, prognostic, and therapeutic purposes.
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