WebSep 1, 2016 · Giant-cell hepatitis (GCH) is characterized by parenchymal inflammation with formation of large multinucleated hepatocytes in response to a variety of insults to the liver. Although it is commonly described in neonates, it rarely occurs in adults. WebWe conclude that syncytial giant-cell hepatitis is a heretofore unrecognized form of paramyxoviral infection that is severe and for which the prognosis is poor. Funding and Disclosures

Giant-cell Hepatitis—Rare Entity in Adults - ScienceDirect

WebGiant cell hepatitis (CGH) with autoimmune haemolytic anaemia (AHA) is a distinct entity with an aggressive course. Immunosuppression may help early disease. A case is reported of a child with GCH and AHA with early … WebGiant cell hepatitis (GCH) is a pathologic diagnosis characterized by liver inflammation and large multinucleated hepatocytes. GCH is a common pathologic entity in infants but is exceedingly rare in adults. It is typically in response to drugs, autoimmune hepatitis (AIH), viruses and malignancy. bank pekao sa in usa

Neonatal giant cell hepatitis: histological and etiological …

WebIntroduction The evaluation of prolonged obstructive jaundice in infancy, involving primarily the differential diagnosis between "giant-cell hepatitis" and biliary atresia, remains a difficult clinical problem. In spite of reports concerning the diagnostic usefulness of cholagogue administration, duodenal intubation, SGOT determinations, 1 administration … WebGiant cell hepatitis (GCH) is a pathologic diagnosis characterized by liver inflammation and large multinucleated hepatocytes. GCH is a common pathologic entity in infants but is … WebApr 16, 2013 · Giant cell hepatitis (GCH) with autoimmune hemolytic anemia (AIHA) is a rare, progressive disorder in infants and young children, which often proves fatal. A child experiencing GCH with AIHA usually develops jaundice and hepatitis at approximately 1 year of age along with AIHA and a positive direct Coombs test. The diagnosis is usually ... pokenio pontoise