Literature DB >> 11316183

Postinfantile giant cell hepatitis complicating ulcerative colitis: a case report and review of the literature.

J Labowitz1, S Finklestein, M Rabinovitz.   

Abstract

Giant cell hepatitis is common in the neonatal period. When present in adults, it is known as postinfantile giant cell hepatitis (PGCH). PGCH can arise in the context of viral, drug-related, and autoimmune disorders but, in many other cases, its etiology remains unclear. We report a case of PGCH occurring in the setting of autoimmune hepatitis and ulcerative colitis. This case highlights the close association between PGCH and autoimmune disorders and the need to recognize it as a hepatic complication of inflammatory bowel disease.

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Year:  2001        PMID: 11316183     DOI: 10.1111/j.1572-0241.2001.03711.x

Source DB:  PubMed          Journal:  Am J Gastroenterol        ISSN: 0002-9270            Impact factor:   10.864


  3 in total

1.  Postinfantile giant cell hepatitis: an etiological and prognostic perspective.

Authors:  Chhagan Bihari; Archana Rastogi; Shiv Kumar Sarin
Journal:  Hepat Res Treat       Date:  2013-03-11

2.  Postinfantile Giant Cell Hepatitis with Features of Acute Severe Autoimmune Hepatitis Probably Triggered by Diclofenac in a Patient with Primary Myelofibrosis.

Authors:  Pinelopi Arvaniti; Kalliopi Zachou; George K Koukoulis; George N Dalekos
Journal:  Case Reports Hepatol       Date:  2018-03-11

3.  Post-infantile giant cell hepatitis: A single center's experience over 25 years.

Authors:  Bassem Matta; Ricardo Cabello; Mordechai Rabinovitz; Marta Minervini; Shahid Malik
Journal:  World J Hepatol       Date:  2019-12-27
  3 in total

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