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Acute Calculous Cholecystitis Presenting as an Acute Abdomen in a Five-Month-Old Child
Estela Kakoo Brioso1, Joana Jonet2, Sofia M Antunes2
1Pediatrics, Hospital De Cascais Dr. José De Almeida, Lisbon, PRT.
Insights
Acute cholecystitis, rare in infants, requires consideration for acute abdomen. This case highlights non-surgical management of pediatric gallstone disease, emphasizing prompt therapy to prevent complications.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Surgical Pediatrics
Background:
- Acute cholecystitis is uncommon in young children, often presenting as an acute abdomen.
- Early diagnosis and management are crucial to prevent severe complications.
Observation:
- A five-month-old male presented with crying, poor feeding, vomiting, diarrhea, and right upper quadrant tenderness.
- Laboratory tests showed elevated gamma-glutamyl transferase and alkaline phosphatase.
- Abdominal ultrasound suggested acute calculous cholecystitis.
Findings:
- The patient was successfully treated with intravenous hydration and antibiotics, avoiding surgery.
- A calcium bilirubinate calculus was found in stool, but the etiology remained undetermined.
- This case underscores the possibility of gallstone disease in infants.
Implications:
- Highlights the importance of considering acute cholecystitis in pediatric acute abdomen evaluations.
- Demonstrates the potential for non-operative management in select pediatric cases.
- Emphasizes the need for prompt therapeutic intervention to mitigate risks associated with pediatric gallstone disease.
Abstract:
Acute cholecystitis is an exceedingly rare condition in young children; nevertheless, it should be considered while investigating an acute abdomen. We report a case of a five-month-old male who presented to the pediatric emergency department with inconsolable crying, decreased oral intake, vomiting, diarrhea, and a tender right upper quadrant of the abdomen. Laboratory studies revealed elevated gamma-glutamyl transferase and alkaline phosphatase and the abdominal ultrasound was suggestive of acute calculous cholecystitis. The patient was treated with intravenous hydration and antimicrobial therapy, avoiding the need for emergent cholecystectomy. A calcium bilirubinate calculus was observed in the feces but no etiology was found after extensive investigation. We aim to raise awareness of this diagnosis and the need for prompt initiation of therapy to avoid complications.
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