A Canadian children's hospital's experience with cystic echinococcosis over 30 years: A case series

Author:

Kazmi Kescha1,Krueger Carsten2,Wong Waison1,Baertschiger Reto M3,Hui Charles2,Nagy Anita45,Navarro Oscar M67,Razik Fathima8,Schwartz Kevin L910,Boggild Andrea K111213,Morris Shaun K11014

Affiliation:

1. Division of Infectious Diseases, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada

2. Division of Infectious Diseases, Immunology, and Allergy, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada

3. Division of General and Thoracic Surgery, Department of Surgery, The Hospital for Sick Children, University of Toronto, Ontario, Canada

4. Division of Pathology, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada

5. Department of Pathobiology and Laboratory Medicine, University of Toronto, Toronto, ON, Canada

6. Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada

7. Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada

8. Division of Emergency Medicine, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada

9. Unity Health Toronto, Toronto, Ontario, Canada

10. Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada

11. Tropical Disease Unit, Toronto General Hospital, Toronto, Ontario, Canada

12. Department of Medicine, University of Toronto, Toronto, Ontario, Canada

13. Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada

14. Centre of Global Child Health, Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada

Abstract

Background: Cystic echinococcosis (CE) or hydatid disease caused by the cestode Echinococcus granulosus sensu lato is an uncommon infection in Canada especially among children. There are limited reports describing the clinical presentation and management in Canadian children. Methods: The medical records of all children diagnosed with CE at a quaternary paediatric centre in Ontario between January 1988 and August 2021 were retrospectively reviewed. The clinical course, management, and outcomes of each case were summarized. Results: We report two paediatric cases of cystic echinococcosis (CE) in detail and review four additional cases seen at our institution over 33.5 years. The first case was a previously healthy 12-year-old boy with pulmonary CE resulting in unilateral lung collapse and mediastinal shift, who was presumedly infected while living in the Middle East. The second case was a previously healthy 3-year-old girl with pulmonary CE acquired locally in southern Ontario. Four other cases of CE with hepatic involvement (median age 12.5 years) were identified during the study period. Five out of six patients received both surgical and medical therapy. Conclusion: CE is a rare but serious disease seen in southern Canada that has historically been associated with travel or migration. Due to changes in urban wildlife landscapes and increased global migration, CE may become more prevalent in Canadian children. We describe the first locally acquired case in rural southern Ontario diagnosed at our centre. Prompt recognition of this infection in children by health care providers is important to prevent morbidity and mortality.

Publisher

University of Toronto Press Inc. (UTPress)

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