Human Pathology
Volume 40, Issue 4 , Pages 516-526, April 2009

Clinicopathologic spectrum of massive and submassive hepatic necrosis in infants and children

  • Richard Kirsch, MBChB, PhD, FCPath(Anat), FRCPC

      Affiliations

    • Division of Pathology, Department of Pediatric Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, M5G 1X8 Canada
    • Corresponding Author InformationCorresponding author. Mount Sinai Hospital, 600 University Avenue, Toronto, Canada M5G 1X8.
  • ,
  • Jason Yap, MBChB, FRCAP

      Affiliations

    • Division of Gastroenterology, Hepatology and Nutrition, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, M5G 1X8 Canada
  • ,
  • Eve A. Roberts, MD, FRCPC

      Affiliations

    • Division of Gastroenterology, Hepatology and Nutrition, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, M5G 1X8 Canada
  • ,
  • Ernest Cutz, MD, FRCPC

      Affiliations

    • Division of Pathology, Department of Pediatric Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, M5G 1X8 Canada

Received 23 February 2008; received in revised form 23 July 2008; accepted 28 July 2008. published online 05 January 2009.

Summary 

Clinicopathologic features of 45 patients with fulminant hepatic failure due to massive or submassive hepatic necrosis were studied. Both percutaneous biopsies and liver explants were available in 23 patients, whole livers only in 11 cases, and biopsies only in 11 cases. An etiologic diagnosis was established in 16 cases (36%). A further 3 cases (7%) were associated with aplastic anemia. Established etiologies included drug reactions (n = 7); autoimmune hepatitis, type 2 (n = 3); halothane hepatitis (n = 1); ischemia/hypotension (n = 1); mushroom poisoning (n = 1); mitochondrial disorder (n = 1); hemophagocytic lymphohistiocytosis (n = 1); and adenoviral hepatitis (n = 1). The extent of necrosis on liver biopsy correlated poorly with that in liver explants (mean difference, 32% ± 23.8%). Almost all cases could be classified into one of 2 broad patterns of necrosis, namely, (1) zonal coagulative necrosis or (2) panlobular (nonzonal) necrosis. These patterns differed significantly with respect to several clinical parameters including sex ratio, peripheral blood white cell count, serum aspartate transaminase and alanine transaminase, conjugated bilirubin, and alkaline phosphatase levels. Livers with panlobular necrosis showed a spectrum of histopathologic findings that included central venulitis (76%), lymphocytic infiltration of large duct/gallbladder epithelium (54%), and syncytial giant cell transformation (18%). These features were not seen in livers with zonal coagulative necrosis which frequently showed prominent steatosis (91%). Both patterns of necrosis frequently showed ductular proliferation (100%) and cholangiolitis (80%). The diagnostic yield of ancillary studies (histochemistry, immunohistochemistry, and electron microscopy) was very low (<1%). The small proportion of cases with etiologic diagnoses precluded correlation of clinical and histopathological parameters with specific etiologies. In summary, this study describes the spectrum of changes seen in massive and submassive necrosis in children and identifies clinical features that might differentiate between 2 broad patterns of necrosis.

Keywords: Liver, Failure, Necrosis, Pathology, Children

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PII: S0046-8177(08)00447-4

doi:10.1016/j.humpath.2008.07.018

Human Pathology
Volume 40, Issue 4 , Pages 516-526, April 2009