| Literature DB >> 21686719 |
Valerio Nobili1, Andrea Pietrobattista, Paola Francalanci, Ilaria Giovannoni, Matilde Marcellini, Sandro Vento.
Abstract
A 1-month-old child presented to our unit with jaundice and raised aminotransferases, γ-glutamyltranspeptidase and bilirubin. Metabolic diseases were ruled out and ultrasound found no alterations. Human herpesvirus type 6 (HHV-6) DNA was found in blood and saliva and IgG anti-HHV-6 in serum, and a diagnosis of HHV-6 hepatitis was made. In the following weeks, aminotransferase values remained raised while γ-glutamyltranspeptidase levels returned to normal in 45 days. At the age of 5 months symptoms and elevated aminotransferases persisted and immunohistochemistry performed on liver tissue allowed a diagnosis of progressive familiar intrahepatic cholestasis type 2 to be made. The patient is now 7 months old, and cholestatic jaundice and pruritus continue to be present.Entities:
Year: 2009 PMID: 21686719 PMCID: PMC3030304 DOI: 10.1136/bcr.08.2008.0623
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X