Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachioji, Tokyo, 1930998, Japan.
Departmet of Diagnostic Pathology, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachioji, Tokyo, 1930998, Japan.
BMC Surg. 2020 Oct 29;20(1):257. doi: 10.1186/s12893-020-00921-6.
Idiopathic portal hypertension (IPH) generally has a good prognosis and rarely results in liver transplantation. Furthermore, there are few reports of living donor liver transplantation (LDLT) for IPH with extrahepatic portal vein stenosis.
We report the case of a 51-year-old female patient diagnosed with IPH more than 20 years ago. She suffered severe jaundice, massive ascites, and encephalopathy at the time of her visit to our hospital. The patient's extrahepatic portal vein showed a scar-like stenosis, and the portal flow was completely hepatofugal. Collateral circulation such as the splenorenal shunt was well developed, and multiple splenic artery aneurysms up to 2 cm were observed in the splenic hilum. Her Model for End-Stage Liver Disease score increased to over 40 because of renal dysfunction, requiring temporary dialysis. We performed LDLT using her husband's right lobe graft and splenectomy. The extrahepatic stenotic portal vein was completely resected, and the superficial femoral vein (SFV) graft collected from the recipient's right leg was used for portal reconstruction as an interposition graft. Although the clinical course after LDLT had many complications, the patient was discharged on postoperative day 113 and has been fine for 2 years after LDLT. Histopathologically, the explanted liver had obliterative portal venopathy, nodular regenerative hyperplasia, and incomplete septal cirrhosis.
This case showed that severe IPH is occasionally associated with extrahepatic portal vein stenosis and can be treated with LDLT with portal vein reconstruction using an interposition graft. It was also suggested that the SFV is a useful choice for the interposition graft.
特发性门静脉高压症(IPH)一般预后良好,很少导致肝移植。此外,关于伴有肝外门静脉狭窄的 IPH 行活体肝移植(LDLT)的报道较少。
我们报告了一例 51 岁女性患者,20 多年前被诊断为 IPH。她来我院就诊时出现严重黄疸、大量腹水和肝性脑病。患者的肝外门静脉呈瘢痕样狭窄,门静脉血流完全向肝背向。侧支循环如脾肾分流良好,脾门处可见多个直径达 2cm 的脾动脉动脉瘤。由于肾功能不全,患者的终末期肝病模型评分增加到 40 以上,需要临时透析。我们为患者行 LDLT,使用其丈夫的右叶供肝和脾切除术。完全切除肝外狭窄门静脉,用取自受者右下肢的股浅静脉(SFV)移植物作为间置移植物进行门静脉重建。尽管 LDLT 后的临床过程中有许多并发症,但患者在术后第 113 天出院,LDLT 后 2 年情况良好。组织病理学检查显示,切除的肝脏有闭塞性门静脉病、结节性再生性增生和不完全间隔性肝硬化。
本病例表明,严重的 IPH 偶尔与肝外门静脉狭窄相关,可通过 LDLT 联合间置移植物门静脉重建进行治疗。此外,SFV 是间置移植物的一种有效选择。