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先天性门静脉缺如的肝母细胞瘤——病例报告

Hepatoblastoma with congenital absence of the portal vein - a case report.

作者信息

Kawano S, Hasegawa S, Urushihara N, Okazaki T, Yoshida A, Kusafuka J, Mimaya J, Horikoshi Y, Aoki K, Hamazaki M

机构信息

Department of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka, Japan.

出版信息

Eur J Pediatr Surg. 2007 Aug;17(4):292-4. doi: 10.1055/s-2007-965448.

Abstract

A 17-month-old girl who had been followed up as an extremely-low-birth-weight infant presented with hepatoblastoma in the right lobe of her liver. Preoperative angiography revealed an absence of the portal vein, and the visceral venous return was through the left renal vein into the inferior vena cava. No liver dysfunction and no jaundice were found; however, a marked elevation of the alpha-fetoprotein level was noted. She underwent a typical right hepatic lobectomy successfully after chemotherapy and has no evidence of recurrence 6 months after surgery.

摘要

一名曾作为极低出生体重儿接受随访的17个月大女孩,出现了肝脏右叶肝母细胞瘤。术前血管造影显示门静脉缺如,内脏静脉回流通过左肾静脉进入下腔静脉。未发现肝功能障碍和黄疸;然而,甲胎蛋白水平显著升高。化疗后,她成功接受了典型的右肝叶切除术,术后6个月无复发迹象。

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