Histological and immunohistochemical features in fatal acute fulminant hepatitis E

Indian J Pathol Microbiol. 2012 Jan-Mar;55(1):22-7. doi: 10.4103/0377-4929.94849.

Abstract

Background: Hepatitis E is being increasingly recognized as an emerging infection in developed countries. Data on histological findings and nature of inflammatory cell infiltrate in liver in this disease are quite sparse.

Aims: This study was planned to study the histological features and the type of inflammatory infiltrate in liver biopsies of patients with acute fulminant hepatitis E.

Materials and methods: We retrieved postmortem liver biopsies of 11 Indian patients with fulminant hepatitis E, and compared these with biopsies from seven patients with fulminant hepatitis B.

Results: Biopsies from acute fulminant hepatitis E showed varying degrees of hepatocyte necrosis, mixed portal and lobular inflammation, accompanied by bile ductular proliferation, lymphocytic cholangitis, Kupffer cell prominence, cholestasis, apoptotic bodies, pseudo-rosette formation, steatosis, and presence of plasma cells in portal tracts. Interface hepatitis was more frequent in acute hepatitis B than in acute hepatitis E (100% vs 20%; P<0.05). These findings differ from those reported in cases with autochthonous hepatitis E in Europe. On immunohistochemistry, lymphocyte infiltrate consisted predominantly of CD3 + T cells in both hepatitis E and hepatitis B; these cells contained a predominant cytotoxic (CD8 + ) cell subpopulation in 81.8% of cases with hepatitis E and in 50% of cases with hepatitis B.

Conclusion: Our findings suggest that histological changes in HEV infection may vary with geographical location because of prevalent HEV genotypes, and that CD8 + lymphocytes play a role in HEV-induced liver injury.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Adult
  • Biopsy
  • CD3 Complex / analysis
  • CD8-Positive T-Lymphocytes / immunology
  • Child
  • Female
  • Hepatitis B / pathology
  • Hepatitis E / pathology*
  • Histocytochemistry
  • Humans
  • Immunohistochemistry
  • Liver / pathology*
  • Male
  • Microscopy
  • Middle Aged
  • Young Adult

Substances

  • CD3 Complex