Cholelithiasis in a toddler with sickle cell disease
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Dana Aronson Schinasi1, Rakesh D Mistry, Rakesh Mistry
1Division of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA. aronsond@email.chop.edu
Insights
Gallstones are uncommon in young children, even those with sickle cell anemia. This case highlights symptomatic gallstones in a toddler with sickle cell disease presenting with abdominal pain.
Area of Science:
- Pediatric Gastroenterology
- Hematology
Background:
- Cholelithiasis (gallstones) is rare in pediatric populations, particularly in toddlers and school-aged children.
- Sickle cell disease (SCD) is a known risk factor for cholelithiasis, though it is still uncommon in young SCD patients.
Observation:
- A toddler with sickle cell disease presented with acute abdominal pain.
- Common causes of abdominal pain in young children with sickle cell disease include vaso-occlusive pain crisis and splenic sequestration.
Findings:
- The toddler was diagnosed with symptomatic cholelithiasis.
- This case underscores that gallstones should be considered in the differential diagnosis of abdominal pain in young children with sickle cell disease.
Implications:
- Early recognition of cholelithiasis in children with sickle cell disease is crucial for timely management.
- This case expands the differential diagnosis of abdominal pain in pediatric sickle cell disease patients.
Abstract:
Cholelithiasis is rarely seen in toddlers and school-aged children, even in the setting of sickle cell anemia. In addition to more common etiologies, such as gastroenteritis, constipation, and urinary tract infection, the differential diagnoses of acute abdominal pain in young children with sickle cell disease include vaso-occlusive pain crisis and splenic sequestration. We describe a case of a toddler with sickle cell disease initially presenting with abdominal pain who was found to have symptomatic cholelithiasis.
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