Primary antiphospholipid syndrome presenting as Budd-Chiari syndrome
نویسندگان
چکیده
منابع مشابه
Hepatic hydatid disease presenting as secondary Budd-Chiari syndrome
To cite: Neelakantan S, Babu AAS, Anandarajan R, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016217118 DESCRIPTION A 51-year-old man presented with a history of vague abdominal pain and progressively increasing abdominal distension. Abdominal examination revealed hepatomegaly with a firm nodular liver palpable below the costal margin with mild tenderne...
متن کاملBudd-Chiari syndrome presenting as fulminant hepatic failure.
Two cases of the Budd-Chiari syndrome are described in whom the diagnosis was finally confirmed at necropsy. The presentation was with encephalopathy, occurring within eight weeks of first symptoms and coming therefore within the definition of fulminant hepatic failure. In one, thought to have non-A, non-B hepatitis, encephalopathy progressed to grade 4 coma with death 12 days after presentatio...
متن کاملBudd-Chiari Syndrome
Budd-Chiari syndrome (BCS) is a rare condition which occurs when there is obstruction of the hepatic veins. It includes any condition in which there is obstruction to venous flow from the small hepatic veins to the inferior vena cava. It should be differentiated from veno-occlusive disease in which the sinusoidal epithelial cells of the hepatic venules are damaged; this mainly occurs after stem...
متن کاملBudd-Chiari syndrome.
Budd-Chiari syndrome is the generic term for different forms of hepatic venous outflow obstruction resulting in a clinical picture of portal hypertension and hepatomegaly. Three levels of venous outflow obstruction may be recognized, affecting respectively the small intrahepatic (IVC). Each level of obstruction is related to a different aetiology. Clinical manifestations range from mild symptom...
متن کامل[Budd Chiari syndrome].
Primary Budd-Chiari syndrome is related to thrombosis of hepatic veins or the terminal portion of the inferior vena cava. This rare disease is usually caused by multiple concurrent factors, including acquired and inherited thrombophilias. Half of the patients with primary Budd-Chiari syndrome are affected with a myeloproliferative disease, the recognition of which is largely based on the assess...
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ژورنال
عنوان ژورنال: Journal of the Japanese Society of Intensive Care Medicine
سال: 2016
ISSN: 1340-7988,1882-966X
DOI: 10.3918/jsicm.23.337