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Published on: April 30, 2019
Sonographic pattern of gallbladder disease in children with sickle cell anaemia
1Department of Radiology, University of Ilorin, Nigeria.
Insights
Gallbladder abnormalities like gallstones and sludge are uncommon in African children with sickle cell anemia. Routine ultrasounds are not recommended due to the low incidence of these findings.
Area of Science:
- Pediatric Hematology
- Gastroenterology
- Medical Imaging
Background:
- Sickle cell anemia is a common hematologic disorder in African populations.
- Gallbladder complications are known in sickle cell disease, but incidence varies geographically.
- Understanding these complications in African children is crucial for appropriate clinical management.
Purpose of the Study:
- To prospectively evaluate the prevalence of gallbladder abnormalities in African children with sickle cell anemia.
- To determine the incidence of cholelithiasis, biliary sludge, and gallbladder wall thickening.
- To assess the relationship between age and the development of these findings.
Main Methods:
- Prospective ultrasound examinations of the gallbladder.
- Study population: 161 children with sickle cell anemia (age range: 2.5 months to 16 years).
- Data collected on cholelithiasis, biliary sludge, and gallbladder wall thickening.
Main Results:
- Cholelithiasis found in 4.2% of patients.
- Biliary sludge present in 7.5%.
- Gallbladder wall thickening noted in 8.1%, the most common abnormality.
Conclusions:
- The incidence of gallbladder stones and sludge in African children with sickle cell anemia is low.
- Dietary and environmental factors may contribute to the low prevalence.
- Routine follow-up ultrasound scans for all sickle cell anemia patients are not justified based on these findings.
Abstract:
A prospective analysis of ultrasound examinations of the gallbladder in 161 children with sickle cell anaemia revealed cholelithiasis in 7 cases (4.2%). Biliary sludge was present in 12 cases (7.5%). The commonest abnormality noted was gallbladder wall thickening seen in 13 patients (8.1%). The age range of patients studied was 2 1/2 months to 16 years with a mean of 7.96 years. The youngest age for development of cholelithiasis was 10 years while biliary sludge was noted earliest at 5 years. Gallbladder wall thickening appeared as early as 4 years. Dietary and environmental factors are probably responsible for the low incidence of cholelithiasis in Africans with sickle cell anaemia. The low incidence of cholelithiasis in the African child with this disease does not justify routine and follow-up ultrasound scans in all cases with sickle cell anaemia.
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