A rare occurrence of primary basal ganglia germinoma in an adult patient

Ebtesam Abdulla, H. Luther, T. Shah, N. Chandran
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Abstract

Background: Basal ganglia germinomas (BGGs) represent a diagnostic and management neurosurgical dilemma. Because of the rarity of these tumors in adults, the management strategies are not well defined.   Case description: A 24-year-old man was presented with progressive left-sided hemiparesis. Cranial computed tomography (CT) and magnetic resonance imaging (MRI) demonstrated a heterogeneous lesion with few microcystic nodules, seen involving the right basal ganglia with calcification. A stereotactic brain biopsy (SBB) was obtained. Histopathology revealed BGG. The patient received whole-brain radiation therapy (WBRT) and reported marked improvement in symptoms with no recurrence during a follow-up period of four years. Conclusion: BGG should be considered a part of the differential diagnosis in young adults presented with hemiparesis and a heterogeneous lesion in the basal ganglia. Standard recommendations for the management of such rare lesions in adults are needed.
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一例罕见的成人原发性基底节生殖细胞瘤
背景:基底节生殖细胞瘤(BGGs)是神经外科诊断和治疗的难题。由于这些肿瘤在成人中很少见,因此管理策略还没有很好的定义。病例描述:一名24岁男子出现进行性左侧偏瘫。颅骨计算机断层扫描(CT)和磁共振成像(MRI)显示了一个异质性病变,伴有少量微囊结节,可见右侧基底节钙化。获得了立体定向脑活检(SBB)。组织病理学显示BGG。患者接受了全脑放射治疗(WBRT),并报告在四年的随访期内症状显著改善,没有复发。结论:BGG应被视为青年轻偏瘫和基底节异质性病变鉴别诊断的一部分。需要对成人这种罕见病变的管理提出标准建议。
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