Portopulmonary hypertension
Portopulmonary hypertension
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DOI：
10.1016/j.ccm.2006.11.004
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发表时间：
2007-03-01
影响因子：
5.7
通讯作者：
Krowka, Michael J.
中科院分区：
文献类型：
--
作者：
Golbin, Jason M.;Krowka, Michael J.
由于原位肝移植的成功，人们对肝病肺血管并发症的诊断和治疗选择越来越感兴趣。这些肺血管并发症的范围从肝肺综合征（其特征是肺内血管扩张）到门脉肺动脉高压（POPH），其特征是由于肺动脉血流阻塞而导致肺血管阻力升高。这篇评论主要集中在 POPH。
As a result of the success of orthotopic liver transplantation, there has been increasing interest in the diagnosis and therapeutic options for the pulmonary vascular complications of hepatic disease. These pulmonary vascular complications range from the hepatopulmonary syndrome, which is characterized by intrapulmonary vascular dilatations, to portopulmonary hypertension (POPH), which is characterized by an elevated pulmonary vascular resistance as a consequence of obstruction to pulmonary arterial blood flow. This review concentrates on POPH.