نتایج جستجو برای: hepatopulmonary syndrome hps

تعداد نتایج: 622675  

2014
Morgen L Govindan Kevin W Kuo Maryam Ghadimi Mahani Thomas P Shanley

INTRODUCTION Hepatopulmonary syndrome is a clinical syndrome that can affect patients of all ages with liver disease and is more common in children with biliary atresia. Contrast echocardiography is the test of choice to diagnose the presence of intrapulmonary vascular dilatation. The established treatment for hepatopulmonary syndrome is liver transplantation. CASE PRESENTATION We present the...

2015
James Offer Lawrence Green Andrew R Houghton Jim Campbell

UNLABELLED This report presents the case of a 42-year-old man with liver cirrhosis who presents with breathlessness. Initial investigations are unable to explain his persistent hypoxia and a diagnosis of hepatopulmonary syndrome is considered. Saline contrast echocardiography is utilised in confirming the diagnosis. Details of this case as well as practicalities in performing and interpreting s...

Journal: :Archivos de bronconeumologia 2006
Brian Vila Auli Diego Pérez García Conrado Fernández Rodríguez Pilar Bañuls Polo Julio Marín Pardo

Hepatopulmonary syndrome consists of a clinical triad: arterial blood deoxygenation, intrapulmonary vasodilation, and liver disease. Both acute and chronic cases of this syndrome have been reported, and the most common cause is cirrhosis. The principle disease mechanism is dilation of the pulmonary blood vessels causing alterations in gas exchange. Increased pulmonary production of nitric acid ...

Journal: :Sudan Journal of Medical Sciences 2007

Journal: :Medizinische Klinik 1990
D J López Aznar L García Sanchís P Bello Arqués J F Martí Vidal A Rivas Sánchez J Alonso Monfort R Pérez Velasco

ANAMNESIS We report about a 60-year-old woman with hepatopulmonary syndrome. The patient suffered from progressive dyspnea and liver cirrhosis following viral hepatitis C, acquired through blood transfusion 30 years ago. EXAMINATION RESULTS Remarkable were clinical signs of chronic liver disease (cutaneous spider naevi, palmar erythema) and signs of chronic respiratory failure (clubbing) with...

Journal: :shiraz e medical journal 2021

Background: Prevention of death in patients on the waiting list for liver transplantation (LT) is a major concern to prioritize organ allocation. Since model end-stage disease (MELD) and its modifications have many shortages, there need further refinement allocation strategy. Objectives: The current study aimed at assessing predictors mortality LT candidates more comprehensive manner with possi...

2017
Hongwei Zhao Fuquan Liu Zhendong Yue Lei Wang Zhenhua Fan Fuliang He

Transjugular intrahepatic portosystemic shunt (TIPS) reduces the portal venous pressure of patients with hepatopulmonary syndrome (HPS).To describe the patients who underwent TIPS for the treatment of HPS.A retrospective study was performed on 81 patients with HPS and gastrointestinal hemorrhage treated with TIPS. Thirty patients underwent TIPS through the main portal vein (group A), 24 through...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2015
Jing Zeng Lin Chen Bing Chen Kaizhi Lu Karine Belguise Xiaobo Wang Bin Yi

BACKGROUND/AIMS Pulmonary microvascular endothelial cell (PMVEC) proliferation and angiogenesis contribute to the development of hepatopulmonary syndrome (HPS). MicroRNA-199a-5p (miR-199a-5p) has emerged as a potent regulator of angiogenesis, and its expression levels significantly decrease in the serum of patients with hepatopathy. However, it has not been reported about whether miR-199a-5p mi...

Journal: :The National medical journal of India 2001
A Mukhopadhya G M Chandy

Hepatopulmonary syndrome consists of a triad of chronic liver disease, pulmonary gas exchange abnormalities and pulmonary vascular dilatation in the absence of detectable cardiopulmonary disease. Patients usually present with symptoms of liver disease and the clinical recognition of this condition is a challenge. Newer non-invasive tests facilitate the diagnosis. Therapeutic strategies for this...

Journal: :Pediatrics 2013
Samuel L Seward William A Gahl

Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disease that displays genetic heterogeneity; there are 9 known subtypes. HPS is characterized by oculocutaneous albinism, a platelet storage pool deficiency and resultant bleeding diathesis, and lysosomal accumulation of ceroid lipofuscin. Patients with HPS, specifically those with the genotypes HPS-1, HPS-2, or HPS-4, are predispose...

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