scholarly journals Budd chiari syndrome: A case report on a rare disorder

2021 ◽  
pp. 377-379
Author(s):  
Akhil Aakunuri ◽  
Saikrishna Mandhala ◽  
Srija Billakuduru ◽  
Akhil Kumar Bavu

Budd Chiari syndrome (BCS) is a rare disease that threatens life due to a hepatic vein blood flow obstruction. As per the literature, thrombosis is a significant factor for hepatic venous obstruction. It can treat BCS based on the severity of the patient’s condition by three methods like hepatic vein angioplasty, interventional radiology stenting with direct intrahepatic portosystemic shunt, or liver transplantation. We describe the case of a 34-years-old female patient who presented with abdominal distension and generalized weakness with a history of BCS. A cooperative collaboration of hepatologists and interventional radiologists helps in effectively treating the syndrome.

2021 ◽  
pp. 153857442110020
Author(s):  
Reza Talaie ◽  
Hamed Jalaeian ◽  
Nassir Rostambeigi ◽  
Anthony Spano ◽  
Jafar Golzarian

Budd-Chiari syndrome (BCS) results from the occlusion or flow reduction in the hepatic veins or inferior vena cava and can be treated with transjugular intrahepatic portosystemic shunt when hepatic vein recanalization fails.1-3 Hypercoagulable patients with primary BCS are predisposed to development of new areas of thrombosis within the TIPS shunt or IVC. This case details a patient with BCS, pre-existing TIPS extending to the right atrium, and chronic retrohepatic IVC thrombosis who underwent sharp recanalization of the IVC with stenting into the TIPS stent bridging the patient until his subsequent hepatic transplantation.


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