Results 21 to 30 of about 353 (131)
A common characteristic of all chronic liver diseases is the occurrence and progression of fibrosis toward cirrhosis. Consequently, liver fibrosis assessment plays an important role in hepatology. Besides its importance for prognosis, determining the level of fibrosis reveals the natural history of the disease and the risk factors associated with its ...
Ludovico Abenavoli +2 more
wiley +1 more source
Primary sclerosing cholangitis (PSC) is a condition of unknown etiology that causes progressive inflammation, fibrosis and obliteration of the intrahepatic and extrahepatic biliary tree. There is no medical cure, and ursodeoxycholic acid and other drugs have not been shown to affect the natural history of the disease.
Young-Mee Lee
wiley +1 more source
Acute graft‐versus‐host disease (GVHD) is a common complication after bone marrow transplantation, with characteristic rash and diarrhea being the most common features. After liver transplantation, however, this phenomenon is very rare. Most transplant patients are on a variety of medications, including immunosuppressants; therefore, the differential ...
Joseph Romagnuolo +3 more
wiley +1 more source
Contribution du Scanner à L’exploration des Pathologies Abdominales à Bangui [PDF]
Introduction : les patients présentant des symptômes digestifs sont soumis à des examens complémentaires d’imagerie médicale dont le scanner. En Centrafrique, le plateau technique était rudimentaire avant l’installation du scanner en 2021.
Kouandongui Bangue, Sougrou Franky +3 more
core +2 more sources
CIRRHOSE ET GROSSESSE A PROPOS D’UN CAS [PDF]
The occurrence of pregnancy on cirrhotic patient is rare because of hypo fertility in this disease. We report a case of a pregnancy in a 23 years old patient with a primitive biliary cirrhosis.
Bennani, O. +5 more
core +2 more sources
Primary Biliary Cirrhosis and Type II Autoimmune Polyglandular Syndrome
A 45‐year‐old female was diagnosed with Hashimoto’s thyroiditis in 1976 and Addison’s disease in 1979. At that time, her antimitochondrial antibody (AMA) level was elevated at 1:32. She subsequently developed premature ovarian failure and type I diabetes mellitus. In 1996, she became jaundiced with a cholestatic enzyme pattern.
Mark Ram Borgaonkar +1 more
wiley +1 more source
Hepatobiliary Tract and Pancreatic Disorders in Celiac Disease
A number of hepatobiliary tract and pancreatic disorders have been documented in patients with celiac disease. Some disorders have shared immunological or genetic factors, including chronic hepatitis, primary biliary cirrhosis and sclerosing cholangitis. Other hepatic or pancreatic pathological changes in celiac disease have been documented with severe
Hugh J Freeman
wiley +1 more source
Une thrombose portale sur coagulopathie révélant une maladie cœliaque : à propos d’une observation exceptionnelle [PDF]
La maladie cœliaque est une entéropathie auto-immune liée à une intolérance au gluten survenant chez des patients génétiquement prédisposés. L’évolution peut être émaillée de complications notamment osseuses, hépatiques, auto-immunes et néoplasiques.
Eddoukani, Imane +1 more
core +2 more sources
Canadian Journal of Gastroenterology and Hepatology, Volume 16, Issue 10, Page 727-732, 2002.
Richard N Fedorak, Desmond J Leddin
wiley +1 more source
Evaluation de la fonction hépatique par ICG Test (IndoCyanine Green Test) [PDF]
Introduction Le carcinome hépatocellulaire (CHC) est le 6ème cancer par ordre de fréquence globale. Il représente la principale cause de décès chez les cirrhotiques.
HURNI, Y.
core

