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Updated: Aug 8, 2026

A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Pathology of chronic hepatitis C in children. Child Liver Study Group of Japan
M Kage1, T Fujisawa, K Shiraki
1First Department of Pathology, Kurume University School of Medicine, Fukuoka, Japan.
Insights
Pediatric chronic hepatitis C (CHC) predominantly shows mild fibrosis. Some children exhibit hemosiderosis and lobular distortion, potentially worsened by frequent blood transfusions.
Area of Science:
- Pediatric Hepatology
- Viral Hepatitis Histopathology
- Immunology
Background:
- Limited data exists on the liver histology of pediatric hepatitis C virus (HCV) infection.
- Understanding these patterns is crucial for managing CHC in children.
Purpose of the Study:
- To characterize the histological patterns of chronic hepatitis C (CHC) in pediatric patients.
- To correlate histological findings with disease severity and identify specific pediatric features.
Main Methods:
- Liver biopsy specimens from 109 pediatric CHC patients were analyzed.
- Histological evaluation used numerical scoring for fibrosis stage, necroinflammation (portal/lobular), and a final grade.
- Assessment included characteristic lesions like lymphoid aggregates and bile duct injury.
Main Results:
- No cirrhosis was observed; 97% of patients had mild fibrosis (stage 1 or 2).
- Four patients were stage 3, two with hemosiderosis.
- Significant correlation found between fibrosis stage and final grade (r = .59, P < .0001).
- Histological features similar to adult CHC were present, including lymphoid aggregates, bile duct injury, and fatty changes.
Conclusions:
- The majority of pediatric CHC cases present with mild fibrosis.
- A subset of children show CHC with lobular distortion and hemosiderosis.
- Frequent blood transfusions may exacerbate hepatic lesions in pediatric CHC.
Abstract:
Limited information is available regarding the histology of hepatitis C virus infection in children. The aim of this study was to determine the histological pattern of chronic hepatitis C (CHC) in children, and liver biopsy specimens from 109 pediatric patients with CHC were examined. Each biopsy specimen was evaluated based on a numerical scoring system for the stage of fibrosis (1-4), the grade of portal/periportal necroinflammation (0-4), the grade of lobular necroinflammation (0-4), and their sum (final grade). The histological lesions considered to be characteristic of chronic hepatitis were also evaluated. None of the children had liver cirrhosis, and 105 cases (97%) were stage 1 or 2. Only 4 children were stage 3. Two of these 4 cases showed hemosiderosis. A significant correlation was observed between the staging score and the final grade in the pediatric patients (r = .59; P < .0001). The histological characteristics of adult CHC, such as lymphoid aggregate, bile duct injury, and fatty changes, were also observed in the children. In conclusion, the majority of children with CHC presented with mild fibrosis, but a few showed CHC with lobular distortion and hemosiderosis. Frequent blood transfusion may aggravate hepatic lesions in pediatric CHC.
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