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首页> 外文期刊>Journal of Neuro-Oncology >Bifocal mixed germ-cell tumor with growing teratoma syndrome and metachronous mature metastases: case report
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Bifocal mixed germ-cell tumor with growing teratoma syndrome and metachronous mature metastases: case report

机译:双灶性混合生殖细胞瘤伴畸胎瘤综合症和异时成熟转移:病例报告

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The authors report the case of a 16-year-old male who presented with a bifocal diencephalic tumor arising both in the neurohypophysis and the pineal region with hydrocephalus. The histological diagnosis obtained during endoscopic ventriculocisternostomy was germinoma. MRI revealed an increase of the neoplasm during chemotherapy with recurrent obstructive hydrocephalus. A new ventriculostomy was performed followed by total surgical resection. The final histopathological analysis demonstrated an immature teratoma. Subsequently, this patient developed metachronous cystic metastases in the cerebello-pontine angles, which were resected and identified as mature teratoma, then we observed a lesion of the brachium conjunctivum which stayed stable after 29 consecutive months. The patient is alive and feels well 6 years after the initial diagnosis and 5 years after the first metastasis. To our knowledge, this is the fifth case of the growing teratoma syndrome located in the brain but the first case with simultaneously bifocal location and infratentorial disseminated metastasis. Obviously surgical removal is the treatment of reference for teratomas. Metastases of teratoma can be mature and may be amenable to surgery with a favorable outcome. Primary intracranial germ-cell tumors (CGT) arise in the midline of the brain and are located in the diencephalon. The peak incidence occurs during the second decade of life. Germ cell tumor (CGT) includes germinomas and non-germinomatous tumors, mature and immature teratomas account for 19.6 % [1]. Curiously, teratomas are able to grow during the first weeks of chemotherapy while serum markers remain normal. This situation was originally described and designed as “the growing teratoma syndroma” (GTS) in primary testis tumors by Logothetis in 1982 [2]. Here we report the rare occurrence of a GTS in a teenager who presented metachronous cystic metastases located in posterior fossa which were histologically mature.
机译:作者报告了一例16岁男性,患有双灶性双脑性肿瘤,该双灶性双脑性肿瘤出现在神经垂体和脑积水的松果体区域。内镜下心室鼻尾吻合术中获得的组织学诊断为生殖细胞瘤。 MRI显示,复发性阻塞性脑积水在化疗期间肿瘤增多。进行新的脑室造口术,然后进行全手术切除。最终的组织病理学分析显示畸胎瘤未成熟。随后,该患者在小脑桥脑角发生了异时性囊性转移,将其切除并鉴定为成熟的畸胎瘤,然后我们观察到结膜分支的病变在连续29个月后保持稳定。病人还活着,在最初诊断后6年和第一次转移后5年感觉良好。据我们所知,这是大脑中正在生长的畸胎瘤综合症的第五例,但同时存在双焦点位置和下腹扩散性转移。显然,手术切除是畸胎瘤的参考治疗。畸胎瘤的转移可能已经成熟,可以接受手术治疗并获得良好的结果。颅内生殖细胞原发性肿瘤(CGT)发生在大脑中线,位于中脑。发病高峰发生在生命的第二个十年。生殖细胞肿瘤(CGT)包括生殖瘤和非生殖细胞瘤,成熟和未成熟的畸胎瘤占19.6%[1]。奇怪的是,畸胎瘤能够在化疗的最初几周内生长,而血清标志物却保持正常。这种情况最初由Logothetis于1982年描述并设计为原发性睾丸肿瘤中的“生长性畸胎瘤综合征”(GTS)[2]。在这里,我们报道了在青少年中出现GTS的罕见情况,该青少年表现出位于后颅窝的组织性成熟的异时性囊性转移。

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