Yolk sac tumor in sigmoid colon with liver metastasis: A rare case report

R. Muddasetty, Basant Mahadevappa, Vishwajeeth Pai, H. R. Jeevan, Junior Consultant, th Main
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Abstract

Extragonadal germ cell tumor (EGGCT) is a rare tumor of primordial germ cells. They commonly involve the central nervous system and anterior mediastinum. The gastrointestinal system is a rare site for EGGCTs. Here, we present the case of a 34-year-old lady who presented with bleeding per rectum. She was evaluated with colonoscopy which showed a growth in the sigmoid colon and biopsy suggestive of poorly differentiated adenocarcinoma. Further evaluation showed multiple liver metastases. Considering colorectal liver metastasis, she was treated with liver-directed neoadjuvant chemotherapy. Following four cycles of chemotherapy, she underwent anterior resection of the sigmoid colon and microwave ablation of the liver metastasis. The final histopathological examination changed the diagnosis as yolk sac tumor. She is currently receiving chemotherapy. Proper small biopsy evaluation with immunohistochemical staining especially when it was a poorly differentiated adenocarcinoma would have prompted us for an appropriate neoadjuvant therapy to improve patient outcome.
乙状结肠卵黄囊肿瘤伴肝脏转移:罕见病例报告
生殖细胞瘤(EGGCT)是一种罕见的原始生殖细胞肿瘤。它们通常累及中枢神经系统和前纵隔。胃肠道系统是 EGGCT 的罕见部位。在此,我们介绍了一例 34 岁女性直肠出血的病例。她接受了结肠镜检查,结果显示乙状结肠有生长,活检提示为分化较差的腺癌。进一步的评估显示有多处肝转移。考虑到结直肠肝转移,她接受了肝脏导向的新辅助化疗。化疗四个周期后,她接受了乙状结肠前切除术和肝转移灶微波消融术。最后的组织病理学检查将其诊断为卵黄囊肿瘤。她目前正在接受化疗。如果能对小活检进行适当的免疫组化染色评估,尤其是当它是分化较差的腺癌时,我们就可以采取适当的新辅助治疗,从而改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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