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小儿原位活体供肝肝移植可治愈Ib型阿伯内西畸形所致的肺动脉高压。

Pediatric orthotopic living-donor liver transplantation cures pulmonary hypertension caused by Abernethy malformation type Ib.

作者信息

Hori Tomohide, Yonekawa Yukihide, Okamoto Shinya, Ogawa Kohei, Ogura Yasuhiro, Oike Fumitaka, Takada Yasutsugu, Egawa Hiroto, Nguyen Justin H, Uemoto Shinji

机构信息

Department of Hepato-pancreato-biliary, Transplant and Pediatric Surgery, Kyoto University Hospital, Kyoto, Japan.

出版信息

Pediatr Transplant. 2011 May;15(3):e47-52. doi: 10.1111/j.1399-3046.2009.01269.x.

Abstract

A 3.3-yr-old boy was diagnosed with PH caused by a PSS of Abernethy malformation type Ib. After control of PH, he underwent OLDLT at 4.9 yr. His PV flowed directly into the confluence of the CCLMHV and the IVC. To shorten the anhepatic phase, hepatic arterial flow was partially maintained. Removal of the native liver began simultaneously with the graft harvest. The proximal PV was cut at the optimal point for reconstruction. The distal PV was cut at the concrescence of the PV and the CCLMHV. After IVC-plasty, the LHV of the graft was attached with an anterior patch by venous grafting and was then anastomosed to the IVC. Although the mPAP temporarily increased above the mean arterial pressure, mPAP was stable during OLDLT. FNH and steatosis were confirmed histopathologically. In summary, pediatric OLDLT was performed successfully in PH caused by PSS.

摘要

一名3.3岁男孩被诊断为因I b型阿伯内西畸形的门静脉分流(PSS)导致的门静脉高压(PH)。在控制门静脉高压后,他于4.9岁时接受了原位肝移植(OLDLT)。他的门静脉直接流入肝中静脉左支(CCLMHV)与下腔静脉(IVC)的汇合处。为缩短无肝期,部分维持了肝动脉血流。在获取供肝的同时开始切除病肝。在最佳重建点切断近端门静脉。在门静脉与CCLMHV的汇合处切断远端门静脉。在下腔静脉成形术后,通过静脉移植用前壁补片连接移植肝的左肝静脉(LHV),然后将其吻合至下腔静脉。尽管平均肺动脉压(mPAP)暂时升高至高于平均动脉压,但在原位肝移植期间mPAP保持稳定。组织病理学证实存在局灶性结节性增生(FNH)和脂肪变性。总之,成功地对因门静脉分流导致的门静脉高压患儿实施了原位肝移植。

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