Mercado M A, Chan C, Zenteno-Guichard G, Vásques M, Hernández J, Orozco H
Portal Hypertension Clinic, Instituto Nacional de la Nutricion, Salvador Zubiran, México, DF, México.
HPB Surg. 1999;11(3):157-62. doi: 10.1155/1999/30698.
Hemorrhagic portal hypertension, secondary to both intrahepatic and extrahepatic portal hypertension, is an uncommon entity. In this condition, the extrahepatic and the intrahepatic obstruction of the portal vein, due to chronic liver disease, produce a more severe form of hemorrhagic portal hypertension that is more difficult to control. The results of surgical treatment (modified Sugiura-Futagawa operation) in this subset of patients is analyzed.
Among 714 patients with a history of hemorrhagic portal hypertension, 14 cases were found with histologically proven liver cirrhosis and complete splenomesoportal thrombosis demonstrated by means of preoperative angiography. Patients with incomplete (partial) splenomesoportal thrombosis were excluded. There were nine males and 5 females with a mean age of 51 years. Alcoholic cirrhosis was demonstrated in 50% of the cases, post hepatitic cirrhosis in 28%, primary biliary cirrhosis in 7%, and cryptogenic cirrhosis in 14%. There were nine Child-Pugh A and 5 B cases. All cases were treated by means of our modified Sugiura-Futagawa procedure.
Bleeding recurrence from esophagogastric varices was shown in one case, colonic varices in one case and hypertensive gastropathy in another of the survivors. Post operative encephalopathy was shown in 3 of the cases. The thirty-six month survival rate was 30% (Kaplan-Meier).
The combination of intrahepatic plus extrahepatic portal hypertension has a worse prognosis. Treatment options are limited (sclerotherapy and/or devascularization), because shunt surgery, TIPS and liver transplantation have a very restricted role and postoperative outcome is poor.
继发于肝内和肝外门静脉高压的出血性门静脉高压是一种罕见的病症。在这种情况下,由于慢性肝病导致的肝外和肝内门静脉阻塞会产生一种更严重的出血性门静脉高压形式,更难以控制。分析了该亚组患者手术治疗(改良的杉浦-二川手术)的结果。
在714例有出血性门静脉高压病史的患者中,14例经组织学证实为肝硬化,术前血管造影显示完全性脾-门静脉血栓形成。排除脾-门静脉血栓形成不完全(部分)的患者。有9例男性和5例女性,平均年龄51岁。50%的病例为酒精性肝硬化,28%为肝炎后肝硬化,7%为原发性胆汁性肝硬化,14%为隐源性肝硬化。有9例Child-Pugh A级和5例B级病例。所有病例均采用我们改良的杉浦-二川手术治疗。
存活患者中,1例出现食管胃静脉曲张出血复发,1例出现结肠静脉曲张出血复发,另1例出现高血压性胃病出血复发。3例出现术后脑病。36个月生存率为30%(Kaplan-Meier法)。
肝内加肝外门静脉高压的联合预后较差。治疗选择有限(硬化疗法和/或去血管化),因为分流手术、经颈静脉肝内门体分流术(TIPS)和肝移植的作用非常有限,且术后结果不佳。