A. Vulin, I. Popov, M. Stefanovic, D. Zivkov-Saponja, A. Stojsic-Milosavljevic
{"title":"右心衰作为门脉性肺动脉高压的首次表现","authors":"A. Vulin, I. Popov, M. Stefanovic, D. Zivkov-Saponja, A. Stojsic-Milosavljevic","doi":"10.2298/sarh221120021v","DOIUrl":null,"url":null,"abstract":"Introduction. Pulmonary artery hypertension and right ventricular failure are potentially fatal complications that can develop in patients with portal hypertension. The objective of this case report was to report a patient with end stage liver disease, and portal and pulmonary artery hypertension and right heart failure. Case outline A 57-year-old man was admitted to the Cardiology Department of tertiary hospital due to signs of right sided heart failure, ascites, pleural effusions, and pretibial edema. The patient had the history of alcohol abuse, arterial hypertension and gout. Just prior to the admission, abdominal ultrasound revealed granular liver structure, as well as ascites. Laboratory tests showed microcytic anemia, values of transaminases below referent, hypoalbuminemia, low creatinine clearance. Echocardiography revealed pulmonary hypertension (PH) and right ventricle failure. Right heart catheterization unraveled precapillary PH, but thoracic CT scan and thoracocentesis excluded underlying pulmonary illness. Treatment continued at Gastroenterology department of tertiary hospital. Abdominal CT scan diagnosed cirrhotic liver, and signs of portal hypertension. The patient was treated with symptomatic therapy, but develop acute on chronic renal failure and eventually died. Conclusion. Multidisciplinary approach is very important to distinguish portopulmonary hypertension early in the course of liver disease, because evolution of right sided heart failure precludes these patients from adequate lifesaving therapy.","PeriodicalId":22263,"journal":{"name":"Srpski arhiv za celokupno lekarstvo","volume":"1 1","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Right-sided heart failure as a first presentation of portopulmonary hypertension\",\"authors\":\"A. Vulin, I. Popov, M. Stefanovic, D. Zivkov-Saponja, A. Stojsic-Milosavljevic\",\"doi\":\"10.2298/sarh221120021v\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction. Pulmonary artery hypertension and right ventricular failure are potentially fatal complications that can develop in patients with portal hypertension. The objective of this case report was to report a patient with end stage liver disease, and portal and pulmonary artery hypertension and right heart failure. Case outline A 57-year-old man was admitted to the Cardiology Department of tertiary hospital due to signs of right sided heart failure, ascites, pleural effusions, and pretibial edema. The patient had the history of alcohol abuse, arterial hypertension and gout. Just prior to the admission, abdominal ultrasound revealed granular liver structure, as well as ascites. Laboratory tests showed microcytic anemia, values of transaminases below referent, hypoalbuminemia, low creatinine clearance. Echocardiography revealed pulmonary hypertension (PH) and right ventricle failure. Right heart catheterization unraveled precapillary PH, but thoracic CT scan and thoracocentesis excluded underlying pulmonary illness. Treatment continued at Gastroenterology department of tertiary hospital. Abdominal CT scan diagnosed cirrhotic liver, and signs of portal hypertension. The patient was treated with symptomatic therapy, but develop acute on chronic renal failure and eventually died. Conclusion. Multidisciplinary approach is very important to distinguish portopulmonary hypertension early in the course of liver disease, because evolution of right sided heart failure precludes these patients from adequate lifesaving therapy.\",\"PeriodicalId\":22263,\"journal\":{\"name\":\"Srpski arhiv za celokupno lekarstvo\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Srpski arhiv za celokupno lekarstvo\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2298/sarh221120021v\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Srpski arhiv za celokupno lekarstvo","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2298/sarh221120021v","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Right-sided heart failure as a first presentation of portopulmonary hypertension
Introduction. Pulmonary artery hypertension and right ventricular failure are potentially fatal complications that can develop in patients with portal hypertension. The objective of this case report was to report a patient with end stage liver disease, and portal and pulmonary artery hypertension and right heart failure. Case outline A 57-year-old man was admitted to the Cardiology Department of tertiary hospital due to signs of right sided heart failure, ascites, pleural effusions, and pretibial edema. The patient had the history of alcohol abuse, arterial hypertension and gout. Just prior to the admission, abdominal ultrasound revealed granular liver structure, as well as ascites. Laboratory tests showed microcytic anemia, values of transaminases below referent, hypoalbuminemia, low creatinine clearance. Echocardiography revealed pulmonary hypertension (PH) and right ventricle failure. Right heart catheterization unraveled precapillary PH, but thoracic CT scan and thoracocentesis excluded underlying pulmonary illness. Treatment continued at Gastroenterology department of tertiary hospital. Abdominal CT scan diagnosed cirrhotic liver, and signs of portal hypertension. The patient was treated with symptomatic therapy, but develop acute on chronic renal failure and eventually died. Conclusion. Multidisciplinary approach is very important to distinguish portopulmonary hypertension early in the course of liver disease, because evolution of right sided heart failure precludes these patients from adequate lifesaving therapy.
期刊介绍:
Srpski Arhiv Za Celokupno Lekarstvo (Serbian Archives of Medicine) is the Journal of the Serbian Medical Society, founded in 1872, which publishes articles by the members of the Serbian Medical Society, subscribers, as well as members of other associations of medical and related fields. The Journal publishes: original articles, communications, case reports, review articles, current topics, articles of history of medicine, articles for practitioners, articles related to the language of medicine, articles on medical ethics (clinical ethics, publication ethics, regulatory standards in medicine), congress and scientific meeting reports, professional news, book reviews, texts for "In memory of...", i.e. In memoriam and Promemoria columns, as well as comments and letters to the Editorial Board.
All manuscripts under consideration in the Serbian Archives of Medicine may not be offered or be under consideration for publication elsewhere. Articles must not have been published elsewhere (in part or in full).