نتایج جستجو برای: budd chiary syndrome

تعداد نتایج: 622217  

2011
Daniela T Carvalho Fernando T Oikawa Nilce M Matsuda Paulo RB Évora Alice T Yamada

INTRODUCTION The risk that patients with Behçet's disease will develop thrombotic complications has been previously described. Although it is distributed worldwide, Behçet's disease is rare in the Americas and Europe. Even though the pathogenic mechanisms of vascular complications of Budd-Chiari syndrome in patients with Behçet's disease are unknown, severe vascular complications of Budd-Chiari...

Journal: :Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia 2002
Yukio Kuniyoshi Kageharu Koja Kazufumi Miyagi Tooru Uezu Satoshi Yamashiro Katuya Arakaki Katuhito Mabuni Shigenobu Senaha

OBJECTIVE Although Budd-Chiari syndrome in Japanese is usually chronic, and of unknown etiology and idiopathic, Behcet's disease is rare as an underlying disorder of Budd-Chiari syndrome in Japanese. To clarify the Behcet-induced Budd-Chiari syndrome, the clinical course and pathologic findings of patients with Behcet-induced Budd-Chiari syndrome were compared with those of patients with idiopa...

Journal: :Indian pediatrics 2016
Anandini Suri Varun K Sharma Prajakta R Ranade Shaji Marar Aabha Nagral

BACKGROUND Hepatocellular carcinoma is an uncommon complication described in patients with Budd-Chiari syndrome. CASE CHARACTERISTICS A 12-year-old boy with Budd-Chiari syndrome, who was earlier treated with Transjugular intrahepatic porto-systemic shunt (TIPS), presented with acute onset hemoperitoneum and hypotension. OUTCOME It was diagnosed to be a case of ruptured hepatocellular carcin...

Masoud Vafamanesh Mehrosadat Alavi Mohammad Eftekhari,

Filling defects are often observed on 99mTc sulfur colloid liver scans. Hot spots are much less frequently seen. Superior vena cava syndrome is the most frequent cause of this finding. In this report 3 patients with S.V.C and budd - Chiari syndrome with HOT SPOT on liver scan are presented. Mechanisms of scintigraphic patterns are reviewed.

Journal: :Gut 2006
C E Eapen D Velissaris M Heydtmann B Gunson S Olliff E Elias

BACKGROUND We report our experience with management of patients with Budd Chiari syndrome over the past two decades. In 1996 we described a novel approach involving recanalisation of hepatic veins by combined percutaneous and transvenous approaches. This was incorporated into an algorithm published in 1999 in which our preferred treatment for all cases of Budd Chiari syndrome with short segment...

Journal: :Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation 2012
Koray Bas Onur Yaprak Murat Dayangac Onur Levent Ulusoy Gulen Bulbul Dogusoy Yildiray Yuzer Yaman Tokat

Budd-Chiari syndrome is a rare but life-threatening disorder characterized by obstruction of the hepatic venous outflow. Treatment depends on the underlying cause, the location, and extent of the obstruction, and the functional capacity of the liver. A stepwise therapeutic approach is commonly accepted. When all other therapy options are unsuccessful, or in case of end-stage liver disease, tran...

Journal: :middle east journal of digestive diseases 0
neda nozari hassan vossoghinia fatemeh malekzadeh lila kafami mahyar mirheidari reza malekzadeh

background budd-chiari syndrome (bcs) is defined as hepatic venous outflow obstruction (hvoo). bcs is an uncommon, life-threatening liver disorder. this study describes the clinical and etiological characteristics in addition to the long-term outcome of bcs in a single referral center in tehran, iran. methods we reviewed long-term outcome of patients who were diagnosed with bcs between 1989 and...

Journal: :Journal of infection in developing countries 2013
Sami Akbulut Mehmet Yilmaz Aysegul Kahraman Sezai Yilmaz

Budd-Chiari syndrome is an uncommon disorder characterized by the thrombotic or non-thrombotic obstruction of hepatic venous outflow anywhere along the venous course from the hepatic venules to the junction of the inferior vena cava and the right atrium. The etiology of Budd-Chiari syndrome is classified as primary, attributable to intrinsic intraluminal thrombosis or the development of venous ...

2011
Minji Jennifer Kim Yong Suk Jo Jee Hyun Kim Yong-Jin Kim Kyung Hwan Kim Eun Bong Lee Yeong Wook Song Eun Young Lee

Budd-Chiari syndrome has been described as a late complication of Behçet's disease. Although the mortality rate associated with Behçet's disease is low, it can escalate in the presence of Budd-Chiari syndrome and may be further complicated by intracardial thrombus formation. It is therefore important to detect and initiate management early in the disease course. The imaging modalities of choice...

Journal: :Medical ultrasonography 2014
Lavinia Alice Bălăceanu Camelia Cristina Diaconu Gheorghiţa Aron

We report the case of a 84-year-old admitted with symptoms of congestive heart failure. Ultrasonography revealed a hyperechoic nodule in the left lobe of the liver, with a peripheral hypoechoic rim, multiple irregular hypoechoic nodules in both hepatic lobes, portal vein, inferior vena cava, and right atrium thrombosis. On ultrasonographic and alpha-fetoprotein criteria the case was interpreted...

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