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Mixed germ cell tumor and hemangioblastoma in the cerebellum: report of a rare coexistence

机译:小脑混合生殖细胞肿瘤和血管母细胞瘤:罕见并存的报告

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We report a case of a cerebellar tumor consisting of a mixed germ cell tumor (GCT) and a hemangioblastoma. A 22-year-old man presented with myoclonus and cerebellar ataxia. Magnetic resonance imaging showed a tumor mass in the left cerebellar hemisphere. The tumor was totally removed, and the histological diagnosis was an undetermined neoplasm. Ten months later, the patient returned with cerebellar hemorrhage at the site of the previous tumor. An emergency craniotomy was performed, and a tumor mass adjacent to the hematoma was resected. Microscopic examination revealed a mixed GCT consisting of a germinoma, choriocarcinoma, and mature teratomatous component. An area of hemangioblastoma was also found in the same tumor mass. A retrospective examination of the histological sample from the first operation indicated a germinoma. A primary GCT of the posterior fossa is very rare, and there are no other reports of the coexistence of a GCT and a hemangioblastoma. A metastatic GCT lesion of extracranial origin should be considered when the intracranial GCT is non-germinomatous and arises in an unusual site. The most probable hypothesis for the histogenesis of this case was a hemangioblastoma complicated by a “tumor-to-tumor” metastatic lesion of testicular GCT with “burnout” of the primary site.
机译:我们报告由混合生殖细胞肿瘤(GCT)和成血管母细胞瘤组成的小脑肿瘤的一例。一名22岁男子出现肌阵挛和小脑共济失调。磁共振成像显示左小脑半球有肿瘤块。肿瘤已完全切除,组织学诊断为未定肿瘤。十个月后,该患者在先前肿瘤的部位再次出现小脑出血。进行紧急开颅手术,并切除邻近血肿的肿瘤块。显微镜检查显示混合的GCT由生殖细胞瘤,绒毛膜癌和成熟的畸胎瘤成分组成。在相同的肿瘤块中还发现了血管母细胞瘤区域。对第一次手术的组织学样本进行回顾性检查,发现有生殖器瘤。后颅窝的原发性GCT非常少见,尚无其他报道表明GCT与血管母细胞瘤并存。当颅内GCT非生发性并出现在异常部位时,应考虑颅外起源的转移性GCT病变。这种情况下组织发生的最可能假说是成血管母细胞瘤并发睾丸GCT的“肿瘤到肿瘤”转移性病变,并伴有原发部位的“倦怠”。

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