Histopathology of the liver in children with chronic hepatitis C viral infection

Authors

  • Kamran Badizadegan,

    1. Department of Pathology Harvard Medical School, Boston, MA
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  • Maureen M. Jonas,

    1. Center for Childhood Liver Disease, Combined Program in Gastroenterology, Children's Hospital and Harvard Medical School, Boston, MA
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  • Mary Jane Ott,

    1. Center for Childhood Liver Disease, Combined Program in Gastroenterology, Children's Hospital and Harvard Medical School, Boston, MA
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  • Suzanne P. Nelson,

    1. Center for Childhood Liver Disease, Combined Program in Gastroenterology, Children's Hospital and Harvard Medical School, Boston, MA
    Current affiliation:
    1. Children's Memorial Medical Center, Chicago, IL
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  • Antonio R. Perez-Atayde M.D.

    Corresponding author
    1. Department of Pathology Harvard Medical School, Boston, MA
    • Department of Pathology-Bader 1, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115. Fax: (617) 731-0954
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Abstract

Although the epidemiology, natural history, and pathological aspects of chronic hepatitis C are well-defined in the adult population, little is known about the characteristics of chronic hepatitis C infection in children. Reports on the histological features and progression of hepatitis C in children are scarce, and consist primarily of multicenter studies in Japanese and European children. Given the geographic variations in viral genotype and the association of pathology with genotype, whether the Japanese and European studies can be extended to the North American populations is unclear. We report the histopathology of the liver in 40 children with chronic hepatitis C infection treated in a single North American institution. The children included 19 males and 21 females ranging in age from 2.0 to 18.6 years at the time of liver biopsy (mean ± SD: 11.4 ± 4.3 years). Our findings indicate that the characteristic histopathological lesions of chronic hepatitis C infection, including sinusoidal lymphocytosis, steatosis, portal lymphoid aggregates/follicles, and bile duct epithelial damage, occur with approximately the same frequencies in children as have been reported in adults. Necroinflammatory activity was generally mild. Portal fibrosis was present in 78% of the specimens, including fibrous portal expansion (26%), bridging fibrosis (22%), bridging fibrosis with architectural distortion (22%), and cirrhosis (8%). Centrilobular pericellular fibrosis, which has not been previously reported in the context of chronic hepatitis C infection in adults or children, was also a prominent feature in our series, occurring with a similar frequency as steatosis or portal lymphoid aggregates/follicles. Our data suggest that in spite of mild histological necroinflammatory activity in general, the stage of fibrosis in children can be severe in spite of relatively short duration of infection.

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