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Published on: September 16, 2022
Hepatic Cystic Echinococcosis (Hydatid Cyst) in a Six Year Old
A Ali1, K M Butler1, C Brenner2
1Department of Paediatric Infectious Diseases, Children's Health Ireland at Crumlin, Dublin 12.
Insights
Cystic echinococcosis (CE) in children, often asymptomatic, requires considering travel history for diagnosis. Early detection and treatment, including surgery and albendazole, are crucial for managing this parasitic infection.
Area of Science:
- Medical Parasitology
- Pediatric Infectious Diseases
- Hepatology
Background:
- Cystic echinococcosis (CE), caused by Echinococcus granulosus, is a zoonotic parasitic disease.
- While prevalent in some regions, CE cases in children, particularly in Ireland, warrant epidemiological review.
- Asymptomatic liver cysts in children necessitate a thorough differential diagnosis.
Observation:
- A previously healthy 6-year-old girl presented with an asymptomatic liver cyst.
- Diagnostic workup included positive serology for Echinococcus granulosus and suggestive radiological findings.
- Histopathology confirmed CE due to E. granulosus.
Findings:
- The child's infection was likely acquired during travel to continental Europe.
- Surgical resection (liver segmentectomy) combined with pre- and post-operative albendazole treatment was effective.
- This case highlights the importance of considering CE in pediatric liver cystic lesions.
Implications:
- CE should be included in the differential diagnosis for children presenting with asymptomatic liver or lung cysts.
- Eliciting a detailed travel history is critical for diagnosing CE in pediatric cases.
- This case underscores the need for increased awareness of CE in non-endemic areas or among travelers.
Abstract:
Presentation To describe a case of cystic echinococcosis (CE) in a previously healthy child and review epidemiology of CE in Ireland. Diagnosis A previously healthy 6 year old girl was found to have a cystic lesion in the right lobe of her liver. Serology for Echinococcus granulosus was positive, and radiological features were suggestive of CE. Treatment The patient was pre-treated with anti-helminthic medications before undergoing a liver segmentectomy to remove the cyst, and received further treatment with albendazole after surgery. Histological findings were consistent with CE due to E. granulosus, likely acquired during travel to continental Europe. Conclusion CE should be considered in the differential of children with asymptomatic cysts in the liver and/or lung, and a travel history elucidated in such cases.
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