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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Autoimmune hepatitis type-2 and Epstein-Barr virus infection in a toddler: Art of facts or an artifact?

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Author
Zellos, A.; Spoulou, V.; Roma-Giannikou, E.; Karentzou, O.; Dalekos, G. N.; Theodoridou, M.
Date
2013
Keyword
Autoimmune liver diseases
Children
Cholestasis
Epstein-Barr infection
Liver kidney microsome antibodies
alanine aminotransferase
aspartate aminotransferase
azathioprine
microsome antibody
prednisolone
anti liver kidney microsome antibody
anti-liver kidney microsome antibody
autoantibody
alanine aminotransferase blood level
antibody detection
antibody titer
article
artifact
aspartate aminotransferase blood level
autoimmune hepatitis
autoimmune hepatitis type 2
case report
child
cholestatic hepatitis
disease duration
Epstein Barr virus
Epstein Barr virus infection
fatty liver
female
human
liver biopsy
plasma cell
polymerase chain reaction
preschool child
remission
serology
T lymphocyte
treatment outcome
virus inclusion
biopsy
differential diagnosis
immunology
pathology
virus hepatitis
Autoantibodies
Child, Preschool
Diagnosis, Differential
Epstein-Barr Virus Infections
Hepatitis, Autoimmune
Hepatitis, Viral, Human
Humans
Metadata display
Abstract
Epstein-Barr virus (EBV) can cause frequently asymptomatic (or anicteric) and self-limited hepatitis, while occasionally may result in considerable cholestatic hepatitis. Herein, we describe the case of a previously healthy toddler (26 month old girl) with prolonged cholestasis, elevated serum transaminases, EBV serology compatible with recent EBV infection and positive anti liver kidney microsomal antibody type 1 which is characteristic of new-onset autoimmune hepatitis type 2. Liver biopsy was also typical of autoimmune hepatitis as attested by the presence of portal inflammation with predominant T-lymphocytes and plasma cells and interface hepatitis. Persistent EBV-related hepatitis was excluded by the absence of viral inclusions and steatosis on liver specimens and negative liver EBV-PCR. In conclusion, our case strongly suggests that in children with prolonged cholestatic hepatitis, positive EBV serology cannot exclude the presence of other causes of liver disease. In this context, autoimmune hepatitis should be considered as an alternate diagnosis, particularly when there is specific liver-related autoantibody detection. In such conditions, liver biopsy seems mandatory in an attempt to achieve a correct and timely diagnosis of a potentially catastrophic disease as autoimmune hepatitis. Although some cases of autoimmune hepatitis type 1 following EBV infection have been reported in adults, to the best of our knowledge, the present case of autoimmune hepatitis type 2 after EBV infection represents the first case in children ever reported in the English literature.
URI
http://hdl.handle.net/11615/34869
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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