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原发性小脑卵黄囊瘤:病例报告

Primary cerebellar yolk sac tumor: case report.

作者信息

Fujiwara T, Honjo Y, Nagao S, Honda C, Baba Y, Ohmoto T

机构信息

Department of Neurological Surgery, Kagawa Medical School, Mitoyo General Hospital, Okayama University Medical School, Japan.

出版信息

Surg Neurol. 1994 Aug;42(2):121-4. doi: 10.1016/0090-3019(94)90371-9.

DOI:10.1016/0090-3019(94)90371-9
PMID:7522352
Abstract

A rare case of cerebellar yolk sac tumor is described. A 4-year-old boy was admitted for the treatment of a cerebellar tumor and, following total removal of the tumor, he was treated with combination chemotherapy consisting of cisplatin, vinblastine, and bleomycin. He died 18 months after the primary diagnosis due to tumor recurrence. Serum alpha-fetoprotein level was well correlated with the clinical course and the amount of the tumor mass in neuroimaging.

摘要

本文描述了一例罕见的小脑卵黄囊瘤病例。一名4岁男孩因小脑肿瘤入院治疗,肿瘤全切后,接受了顺铂、长春新碱和博来霉素联合化疗。初次诊断18个月后,他因肿瘤复发死亡。血清甲胎蛋白水平与临床病程及神经影像学检查中肿瘤大小密切相关。

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引用本文的文献

1
Primary Yolk Sac Tumor in the Cerebellar Hemisphere: A Case Report and Literature Review of the Rare Tumor.小脑半球原发性卵黄囊瘤:1例报告及该罕见肿瘤的文献综述
Front Oncol. 2021 Nov 5;11:739733. doi: 10.3389/fonc.2021.739733. eCollection 2021.
2
Primary endodermal sinus tumor of the cerebellar hemisphere: a case report with review of the literature.小脑半球原发性内胚窦瘤:一例报告并文献复习
J Neurooncol. 2006 Apr;77(2):173-6. doi: 10.1007/s11060-005-9016-x. Epub 2005 Nov 29.