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Autoimmune hepatitis: trust in transaminases

dc.contributor.authorBrissos, J
dc.contributor.authorCarrusca, C
dc.contributor.authorCorreia, M
dc.contributor.authorCabral, J
dc.date.accessioned2014-04-28T21:06:33Z
dc.date.available2014-04-28T21:06:33Z
dc.date.issued2014
dc.description.abstractA rational and appropriate evaluation of liver biochemical tests is essential, given the increased number of abnormal laboratory results in asymptomatic patients. Critical judgement allows early diagnosis in the absence of typical clinical signs. Autoimmune hepatitis is a rare disease with high clinical variability. We present a child investigated for unexplained increase in aminotransferases, discovered accidentally 2 months earlier in a standard laboratory panel approach. She was asymptomatic and no physical signs of chronic or acute liver disease were found. Laboratory investigation showed hypergammaglobulinaemia with selective elevation of IgG and a positive anti-liver cytosol type 1. Severe interface hepatitis was found on liver biopsy and treatment was initiated with steroids and azathioprine with good response. This case highlights the importance of trusting in any serum aminotransferase abnormality, even in asymptomatic children and emphasises the value of clinical suspicion and specific immunosuppressive therapy in prognosis.por
dc.identifier.citationBMJ Case Rep. 2014 Apr 23;pii: bcr2014203869por
dc.identifier.doi10.1136/bcr-2014-203869
dc.identifier.urihttp://hdl.handle.net/10400.26/6262
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherBMJpor
dc.subjectChildpor
dc.subjectHepatitis, Autoimmunepor
dc.subjectTransaminasespor
dc.subjectCriançapor
dc.subjectHepatite Autoimunepor
dc.titleAutoimmune hepatitis: trust in transaminasespor
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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