医学
卵黄囊
甲胎蛋白
阿尔法(金融)
人口
鉴别诊断
病理
胃肠病学
内科学
胚胎
外科
细胞生物学
肝细胞癌
环境卫生
患者满意度
生物
结构效度
作者
Mai He,Kayla Hoerschgen,Amy E. Armstrong,Lili Zhang,Patrick A. Dillon,Frances V. White,Louis P. Dehner
标识
DOI:10.1080/15513815.2025.2457616
摘要
Introduction: Yolk sac tumor (YST) is a malignant germ cell tumor with 10-15% arising in extragonadal sites. Methods: A search through our institution's database from January 01, 1990, to December 31, 2020, for "yolk sac tumor" or "endodermal sinus tumor" and "liver". Results: Our search yielded three cases. A 20-month-old girl with a liver mass and serum alpha-fetoprotein (AFP) level of 46558.0 ng/mL. The neoplasm was papillary with Schiller-Duval bodies. A 2-year-old boy with hepatic masses and adrenal mass with a serum AFP of 106,604.5 ng/mL. Numerous Schiller-Duval bodies were present. A 7-month-old girl with a liver mass, lung nodules, and retroperitoneal masses. Serum AFP was in the 800s ng/mL. Hepatoid and microcystic YST were mixed with hepatoblastoma (HBL). All three cases were positive for CAM5.2, SALL4, Glypican-3, beta-catenin, and AFP. Conclusion: Hepatic yolk sac tumor should be considered in the differential of a liver mass in pediatric patients with elevated AFP.
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