Uchida Hajime, Sakamoto Seisuke, Shigeta Takanobu, Hamano Ikumi, Kanazawa Hiroyuki, Fukuda Akinari, Karaki Chiaki, Nakazawa Atsuko, Kasahara Mureo
Department of Transplant Surgery, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.
Case Rep Surg. 2012;2012:670289. doi: 10.1155/2012/670289. Epub 2012 Oct 3.
A congenital absence of the portal vein (CAPV) is a rare disorder that may lead to an intrapulmonary shunt. A 14-year-old male with CAPV underwent living donor liver transplantation with a left lobe graft from his father. The portal vein reconstruction was achieved with a renoportal anastomosis using an interpositional graft from the native collateral vein, because portal venous system directly drains to the left renal vein without constructing the confluence of superior mesenteric vein and splenic vein. The patient is doing well with a normal liver function and mild hypoxemia.
先天性门静脉缺如(CAPV)是一种罕见的疾病,可能导致肺内分流。一名患有CAPV的14岁男性接受了活体供肝移植,移植的是来自其父亲的左叶肝脏。门静脉重建通过使用来自天然侧支静脉的间置移植物进行肾门静脉吻合来实现,因为门静脉系统直接引流至左肾静脉,而无需构建肠系膜上静脉和脾静脉的汇合处。患者肝功能正常,有轻度低氧血症,恢复良好。