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Amebic liver abscess in children
Insights
Amebic liver abscess in children is rare but treatable. Early diagnosis and treatment with metronidazole, alongside abscess aspiration, led to no deaths in a pediatric study.
Area of Science:
- Pediatrics
- Infectious Diseases
- Hepatology
Background:
- Amebic liver abscess (ALA) is a significant cause of morbidity and mortality globally.
- Pediatric ALA cases are infrequently reported, necessitating further research into their unique clinical presentations and outcomes.
Purpose of the Study:
- To describe the clinical features, diagnosis, management, and outcomes of amebic liver abscess in children.
- To identify factors contributing to successful treatment of pediatric ALA.
Main Methods:
- Retrospective case series of 24 children diagnosed with ALA between November 1987 and October 1992.
- Diagnosis confirmed via indirect hemagglutination titers and liver ultrasonography.
- Treatment involved metronidazole and, in select cases, abscess aspiration.
Main Results:
- The most common symptoms were high-grade fever and right upper quadrant pain, with tender hepatomegaly.
- Leukocytosis and elevated erythrocyte sedimentation rate were frequent findings.
- Solitary abscesses were predominant (22/24), and jaundice was absent in all pediatric patients.
- No deaths occurred despite a median delay of 15 days in presentation.
Conclusions:
- Pediatric ALA presents differently from adult cases, often without jaundice or significant liver enzyme derangement.
- A high index of suspicion, prompt metronidazole therapy, and judicious abscess aspiration are crucial for favorable outcomes.
- Effective management can significantly reduce the morbidity and mortality associated with pediatric ALA.
Abstract:
Although amebic liver abscess can be a cause of significant morbidity and mortality in all ages, there are few reports dealing with this entity in children. Twenty-four children with amebic liver abscess, ages ranging between 3 weeks and 14.5 years, were managed at the Aga Khan University Hospital, Karachi, Pakistan, between November, 1987, and October, 1992. The most frequent presentation was high grade fever and right upper quadrant pain, associated with tender hepatomegaly, leukocytosis and an elevated erythrocyte sedimentation rate. The diagnosis was confirmed by elevated indirect hemagglutination titers and ultrasonography of the liver. Unlike the experience in adult patients none of the patients had concomitant jaundice, and significant derangement of liver enzymes was unusual. The abscesses were likely to be solitary (22 of 24 patients). There were no deaths despite a mean delay of 15 days before presentation to our hospital. A high index of suspicion, early institution of metronidazole therapy and aspiration of abscesses with potential to rupture are believed to have contributed to the better outcome in these children when compared with results in previous reports.
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