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PedAM

Pediatric Disease Annotations & Medicines




Disease portal hypertension
Phenotype C1619734|pulmonary arterial hypertension
Sentences 12
PubMedID- 23982562 This review summarizes the clinicopathologic features, diagnostic criteria, as well as the latest concepts in the pathogenesis and management of poph, which is defined as is a form of pulmonary arterial hypertension (pah) associated with portal hypertension with or without underlying chronic liver disease.
PubMedID- 25523363 Portopulmonary hypertension represents a serious lung vascular disorder, defined as the presence of pulmonary arterial hypertension that is associated with portal hypertension, with or without the presence of significant liver disease.
PubMedID- 22315210 Portopulmonary hypertension (poph) refers to pulmonary arterial hypertension associated with portal hypertension with or without evidence of an underlying liver disease.
PubMedID- 22447257 Portopulmonary hypertension (poph) refers to the presence of pulmonary arterial hypertension (pah) in patients with portal hypertension.
PubMedID- 24679504 Portopulmonary hypertension (poph) is the presence of pulmonary arterial hypertension in patients with portal hypertension.
PubMedID- 26029592 Poph is defined as pulmonary arterial hypertension with portal hypertension in the absence of other causes of pulmonary arterial hypertension.
PubMedID- 25076996 Portopulmonary hypertension (poph) is defined as pulmonary arterial hypertension (pah) complicated by portal hypertension, with or without advanced hepatic disease.
PubMedID- 24046802 Case report: we report a case of acute right heart pressure overload after surgical correction of the suprahepatic inferior vena cava anastomotic stricture in a 54-year-old woman who had preexisting pulmonary arterial hypertension associated with portal hypertension after orthotopic liver transplantation.
PubMedID- 20677289 pulmonary arterial hypertension (pah) associated with portal hypertension [portopulmonary hypertension (pphtn)] occurs in 2% to 10% of patients with advanced liver disease and carries a very poor prognosis without treatment.
PubMedID- 20351954 Portopulmoanry hypertension (poph) is a form of pulmonary arterial hypertension (pah) associated with portal hypertension with or without underlying chronic liver disease.
PubMedID- 22933880 pulmonary arterial hypertension: an unusual cause of portal hypertension.
PubMedID- 21828952 pulmonary arterial hypertension (pah) in patients with portal hypertension is also referred to as portopulmonary hypertension (pphtn).

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