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Pulmonary Echinococcus in children: A descriptive study in a LMIC
Lunga Mfingwana1, Pierre Goussard1, Lizelle van Wyk1
1Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University and Tygerberg Hospital, Cape Town, South Africa.
Insights
Pulmonary cystic echinococcosis (CE) is common in children, often presenting with cough. Combined medical and surgical treatment is the gold standard for managing this parasitic lung infection.
Area of Science:
- Medical Parasitology
- Pediatric Infectious Diseases
- Public Health
Background:
- Echinococcus granulosus infection poses a significant public health challenge, particularly in lower-middle-income countries.
- Pediatric cases of cystic echinococcosis (CE) frequently involve lung and liver cysts.
Purpose of the Study:
- To characterize a pediatric cohort with pulmonary CE.
- To evaluate the outcomes of combined medical and surgical treatment for pediatric pulmonary CE.
Main Methods:
- Retrospective study conducted at Tygerberg Hospital, South Africa (July 2017 - December 2020).
- Review of clinical, laboratory, radiological, and treatment-related data for pediatric patients.
- Analysis of outcomes for both simple and complicated pulmonary CE cases.
Main Results:
- The study included 35 children (mean age 9.4 years); cough was the most common symptom (93%).
- Isolated pulmonary CE predominated (74%), with left lower lobe involvement.
- 58% had positive indirect hemagglutination assay (IHA) results; complicated CE cases had longer hospital stays.
Conclusions:
- Pulmonary CE is prevalent in children, with extrapulmonary involvement being rare.
- Chest X-ray and CT are key diagnostic tools; IHA serology shows limited utility for pulmonary CE.
- A combined surgical and medical approach is the established treatment for pulmonary CE.
Background:
Echinococcus granulosus is a major public health problem in lower middle-income countries (LMIC). Children are commonly diagnosed with cysts in the lungs and/or the liver.
Objectives:
The purpose of this study was to describe a pediatric cohort diagnosed with pulmonary Cystic Echinococcus (CE) and treated with a combination of medical and surgical therapy.
Methods:
This was a retrospective study performed between July 2017 and December 2020 at Tygerberg Hospital, South Africa. Clinical, laboratory, radiological, medical, and surgery-related outcomes were reviewed.
Results:
The cohort consisted of 35 children, 17 (49%) were male, with a mean age of 9 ± 5.4 years. The most frequently encountered presenting symptom was cough (93%) followed by fever (70%). Isolated pulmonary CE accounted for the majority of cases (74%) with left lower lobe predominance. A significant proportion of the cohort exhibited chest computed tomography (CT) characteristics consistent with complicated pulmonary CE. Eighteen (58%) children had a positive indirect hemagglutination assay (IHA) test result. All children received medical treatment whilst 30 (86%) of children required surgery. Children with complicated pulmonary CE stayed a mean of 12.5 ± 6.6 days, while those with simple cysts stayed 6.8 ± 1.5 days.
Conclusion:
Isolated pulmonary CE is common in children, whereas extrapulmonary cysts are uncommon. Pulmonary CE is diagnosed using chest X-ray and, CT imaging. IHA serology has limited diagnostic utility for pulmonary CE. Combined surgery and chemotherapy remains the gold standard for treating pulmonary CE.
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