Autoimmune hepatitis

Chronic autoimmune hepatitis (AIH) is a rare progressive inflammatory disorder of unknown cause primarily affecting women and associated with circulating autoantibodies, elevated transaminase levels, and increased levels of immunoglobulin.

Giant cell hepatitis

Chronic hepatitis characterized by parenchymal inflammation with formation of large multinucleated hepatocytes in response to a variety of insults to the liver.


Total: 7

                       


(per page)
PMID (PMCID)
29713554
(5866856)
 OTHER
Postinfantile Giant Cell Hepatitis with Features of Acute Severe Autoimmune Hepatitis Probably Triggered by Diclofenac in a Patient with Primary Myelofibrosis.
Arvaniti P, Zachou K, Koukoulis GK, Dalekos GN.
Case Reports Hepatol. 2018;2018:9793868.
Postinfantile Giant Cell Hepatitis with Features of Acute Severe Autoimmune Hepatitis Probably Triggered by Diclofenac in a Patient with Primary Myelofibrosis.
21325763
 FEMALE
A case of adult autoimmune hepatitis with histological features of giant cell hepatitis.
Hayashi H, Narita R, Hiura M, Abe S, Tabaru A, Tanimoto A, Sasaguri Y, Harada M.
Intern Med. 2011;50(4):315-9.
A case of adult autoimmune hepatitis with histological features of giant cell hepatitis.
17074032
 FEMALE Adult
Postinfantile giant-cell hepatitis associated with ulcerative colitis and autoimmune hepatitis.
Anagnostopoulos GK, Margantinis G, Tsiakos S, Kostopoulos P, Grigoriadis K, Arvanitidis D.
J Gastroenterol Hepatol. 2006;21(12):1863-4.
Postinfantile giant-cell hepatitis associated with ulcerative colitis and autoimmune hepatitis.
11843028
 MALE Adult
Post-infantile giant cell hepatitis associated with autoimmune hepatitis and polyarteritis nodosa.
Koskinas J, Deutsch M, Papaioannou C, Kafiri G, Hadziyannis S.
Scand J Gastroenterol. 2002;37(1):120-3.
Post-infantile giant cell hepatitis associated with autoimmune hepatitis and polyarteritis nodosa.
11843028
 MALE Adult
Post-infantile giant cell hepatitis associated with autoimmune hepatitis and polyarteritis nodosa.
Koskinas J, Deutsch M, Papaioannou C, Kafiri G, Hadziyannis S.
Scand J Gastroenterol. 2002;37(1):120-3.
An association between autoimmune hepatitis, polyarteritis nodosa and postinfantile giant cell hepatitis has not been reported previously.
10710079
 FEMALE Adult
Syncytial giant-cell hepatitis due to autoimmune hepatitis type II (LKM1+) presenting as subfulminant hepatitis.
Ben-Ari Z, Broida E, Monselise Y, Kazatsker A, Baruch J, Pappo O, Skappa E, Tur-Kaspa R.
Am J Gastroenterol. 2000;95(3):799-801.
Syncytial giant-cell hepatitis due to autoimmune hepatitis type II (LKM1+) presenting as subfulminant hepatitis.
8878001
 MIXED_SAMPLE Adult
Post-infantile giant cell hepatitis in patients with primary sclerosing cholangitis and autoimmune hepatitis.
Protzer U, Dienes HP, Bianchi L, Lohse AW, Helmreich-Becker I, Gerken G, Meyer zum Buschenfelde KH.
Liver. 1996;16(4):274-82.
Post-infantile giant cell hepatitis in patients with primary sclerosing cholangitis and autoimmune hepatitis.