liver cirrhosis/lafyèv

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[Fever and liver cirrhosis].

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Occurrence of fever in a patient with liver cirrhosis should suggest the following: 1. Endotoxemia. Endotoxins are normally present in portal blood; in hepatic cirrhosis they are insufficiently cleared by the liver and their presence can be demonstrated in the systemic circulation by the "limulus

[The "cryptogenetic" fever of hepatic cirrhosis].

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Pyrexia in Uncomplicated Cirrhosis of the Liver.

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[Loss of weight, languor, pyrexia and a consciousness disorder (glycosuria and csf analysis): (latent cryptococcal meningitis) (pancreatic calculi and portal liver cirrhosis)].

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[A case of Malta fever with multiple phlebitic attacks and liver cirrhosis].

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[A case of juvenile hypersplenomegalic liver cirrhosis (Banti syndrome) characterized by erruptions of herpes labialis and fever of probable viral origin].

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[Fever in the patient with hepatic cirrhosis: 6-month prospective study].

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[A 57-year-old man with diabetes mellitus, liver cirrhosis, ascites and fever].

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[A case of liver cirrhosis complicated by upper gastrointestinal bleeding with pyrexia and intrahepatic space-occupying lesion].

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Hepatic Cirrhosis of Childhood: Intercurrent Typhoid Fever: Death from Acute Yellow Atrophy.

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A case of Sweet's syndrome in a patient with liver cirrhosis caused by chronic hepatitis B.

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Sweet's syndrome (SS), also known as acute febrile neutrophilic dermatosis, is characterized by the sudden onset of painful erythematous skin lesions together with fever and neutrophilia. SS can be associated with several disorders, such as malignancy, autoimmune disease, and infections. However, SS

Chronic Q fever hepatitis complicated by extensive fibrosis.

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Liver involvement is common in acute and chronic Q fever and consists of nonspecific hepatitis and granulomas without fibrosis. We report the case of a patient suffering from chronic Q fever with nonspecific hepatitis and granulomas, in whom progressive development of extensive liver fibrosis was

Improvement of Liver Involvement in Familial Mediterranean Fever After the Introduction of Canakinumab: A Case Report

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Hepatic involvement in familial Mediterranean fever (FMF) ranges from a nonspecific increase in liver enzymes to cryptogenic cirrhosis, and the liver is mostly involved in patients bearing the M694V MEFV mutation in homozygosis. A 44-year-old Jewish woman with FMF developed nonalcoholic

Liver cirrhosis as a delayed complication of Stevens-Johnson syndrome.

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A 26-year-old woman was referred to our department due to fever and skin rash after having taken medication for a common cold. Physical examination revealed erythematous skin changes on her body associated with mucosal involvement in her eyes and oral cavity. Peripheral blood examination revealed

Long-term familial Mediterranean fever remission on successful hepatitis C virus treatment in a patient not responding to colchicine: a case report.

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BACKGROUND Familial Mediterranean fever is an autosomal recessive disorder characterized by periodic febrile attacks of aseptic serositis and/or arthritis. The main treatment is colchicine which prevents attacks in the majority of patients except for a group of colchicine-resistant cases. Chronic

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