- Author:
Jung Sun KIM
1
;
Changhwan KIM
;
Gye Su KIM
;
Dal Soo LIM
;
Hweung Kon HWANG
;
Young Moo RO
Author Information
- Publication Type:Case Report
- Keywords: Hepatopulmonary syndrome; Hypoxemia; Liver cirrhosis; Liver transplantation
- MeSH: Anoxia; Blood Gas Analysis; Dihydroergotamine; Dilatation; Dyspnea; Echocardiography; Hepatopulmonary Syndrome; Humans; Inpatients; Liver; Liver Cirrhosis; Liver Cirrhosis, Alcoholic; Liver Diseases; Liver Transplantation; Male; Microbubbles; Oxygen; Thorax
- From:Tuberculosis and Respiratory Diseases 2009;66(1):47-51
- CountryRepublic of Korea
- Language:Korean
- Abstract: Hepatopulmonary syndrome (HPS) is characterized by a defect in arterial oxygenation that's induced by pulmonary vascular dilatation in the setting of liver disease. Some studies have shown the relationship between the presence of the HPS and the severity of liver disease, but there are only rare cases of HPS inpatient with Child-Pugh class A liver cirrhosis. We report here on a case of a 58 years-old male who suffered from progressive dyspnea for the previous few years. He was diagnosed with alcoholic liver cirrhosis 5 years previously. There was no significant abnormality on the chest radiograph and transthoracic echocardiography, but the arterial blood gas analysis revealed severe hypoxemia. Contrast-enhanced transesophageal echocardiograpy with agitated saline demonstrated a delayed appearance of microbubbles in the left cardiac chambers. Thus, he was finally diagnosed with HPS. This case suggests that we should consider HPS when a patient with compensated liver cirrhosis has unexplained dyspnea.