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肝硬化中的肺血管异常

Pulmonary vascular abnormalities in cirrhosis.

作者信息

Herve Philippe, Le Pavec Jerome, Sztrymf Benjamin, Decante Benoit, Savale Laurent, Sitbon Olivier

机构信息

National French Reference Centre for Pulmonary Arterial Hypertension, UPRES EA 2705, Service de Pneumologie et Réanimation Respiratoire, Hôpital Antoine Béclère, Assistance Publique-Hôpitaux de Paris, Université Paris-Sud, Clamart, France.

出版信息

Best Pract Res Clin Gastroenterol. 2007;21(1):141-59. doi: 10.1016/j.bpg.2006.07.011.

Abstract

Two pulmonary vascular disorders can occur in liver disease and/or portal hypertension: the hepatopulmonary syndrome (HPS), which is characterized by intrapulmonary vascular dilatations, and portopulmonary hypertension (POPH), in which pulmonary vascular resistance is elevated. POPH and HPS are characterized by distinct pulmonary microvascular remodelling, which occurs at different anatomical sites of the pulmonary microcirculation. The exact pathophysiological mechanisms of these pulmonary vascular disorders are unknown. However, as HPS and POPH have been reported in patients with extrahepatic portal hypertension, the factor that determines their development must be portal hypertension. The clinical presentations are very different, with gas exchange impairment in HPS and hemodynamic failure in POPH. The severity of HPS seems to parallel the severity of liver failure, whereas no simple relationship has been identified between hepatic impairment and the severity of POPH. Resolution of HPS is common after liver transplantation, which has an uncertain effect in POPH.

摘要

两种肺血管疾病可发生于肝脏疾病和/或门静脉高压症:肝肺综合征(HPS),其特征为肺内血管扩张;以及门肺高压(POPH),其中肺血管阻力升高。POPH和HPS的特征是不同的肺微血管重塑,发生在肺微循环的不同解剖部位。这些肺血管疾病的确切病理生理机制尚不清楚。然而,由于肝外门静脉高压症患者中已报道了HPS和POPH,决定其发展的因素必定是门静脉高压。临床表现差异很大,HPS有气体交换受损,而POPH有血流动力学衰竭。HPS的严重程度似乎与肝功能衰竭的严重程度平行,而在肝功能损害与POPH的严重程度之间未发现简单的关系。肝移植后HPS常见缓解,而对POPH的影响尚不确定。

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