Magni Elena, Sonzogni Angelica, Zampino Maria Giulia
Medical Care Unit, European Institute of Oncology, Milan, Italy;
Rare Tumors. 2010 Mar 31;2(1):e10. doi: 10.4081/rt.2010.e10.
We describe here a case of pure gastric yolk sac tumor (YST). A 62-year-old patient underwent gastrectomy with D2 dissection. The histological report confirmed the diagnosis of YST and that two of the 14 regional lymph nodes removed were metastatic. Three courses of PEB regimen chemotherapy were delivered subsequently. Three months later the patient experienced dysphagia from stenosis of the anastomosis and a computerized tomography scan showed tumor recurrence with peritoneal nodules; the patient died one year after surgery. The origin of gastric YST is unclear but involvement of migrating germ cells during embryonic development or multipotential neoplastic protoepithelial cells of the gastric mucosa have been suggested. Generally the prognosis of gastric YST is poor and the standard therapeutic approach beyond surgery is still uncertain.
我们在此描述一例纯胃卵黄囊瘤(YST)。一名62岁患者接受了D2根治性胃切除术。组织学报告确诊为YST,且切除的14个区域淋巴结中有两个发生转移。随后进行了三个疗程的PEB方案化疗。三个月后,患者因吻合口狭窄出现吞咽困难,计算机断层扫描显示肿瘤复发并伴有腹膜结节;患者术后一年死亡。胃YST的起源尚不清楚,但有观点认为是胚胎发育过程中迁移的生殖细胞受累,或胃黏膜的多能肿瘤原上皮细胞所致。一般来说,胃YST的预后较差,手术之外的标准治疗方法仍不明确。