Velpula Madhavi, Sheron Nick, Guha Neill, Salmon Tony, Hacking Nigel, Veldtman Gruschen R
Department of Adult Congenital Heart Disease, Cardiothoracic Division, Southampton University Hospital, Southampton, UK.
Congenit Heart Dis. 2011 Mar-Apr;6(2):175-8. doi: 10.1111/j.1747-0803.2010.00451.x. Epub 2011 Mar 1.
We describe the case history of a 42-year-old man with cardiac cirrhosis, portal hypertension, and life-threatening variceal bleeding after Fontan revision surgery. Direct pressure measurements in the portal vein, though high, demonstrated only a modest portosystemic gradient (PSG), 9 mm Hg. A transjugular intrahepatic portosystemic shunt procedure was performed. This reduced the PSG (3 mm Hg). His bleeding was controlled. The patient's histopathological findings were identical to that previously documented in Fontan patients, raising the question of whether these subdiaphragmatic hemodynamics are representative of the broader failing Fontan population.
我们描述了一名42岁男性的病史,该患者患有心源性肝硬化、门静脉高压,并在Fontan修复手术后出现危及生命的静脉曲张出血。门静脉直接压力测量值虽高,但仅显示出适度的门体静脉压力梯度(PSG),为9毫米汞柱。进行了经颈静脉肝内门体分流术。这使PSG降低(至3毫米汞柱)。他的出血得到了控制。患者的组织病理学发现与先前Fontan患者记录的相同,这就提出了一个问题,即这些膈下血流动力学是否代表了更广泛的Fontan功能衰竭人群。