[Isolated gallbladder agenesis mimicking biliary colic: A difficult preoperative diagnosis]
M Bouche1, S Mesureur1, T Forzini1
1Service de chirurgie pédiatrique viscérale, CHU d'Amiens, avenue Laennec-Salouel, 80054 Amiens cedex 1, France.
Summary
Isolated gallbladder agenesis is a rare congenital anomaly. Diagnosis can be challenging, often mistaken for other conditions, leading to potential misdiagnosis and unnecessary surgery.
Area of Science:
- Gastroenterology and Hepatology
- Pediatric Surgery
- Medical Imaging
Background:
- Isolated gallbladder agenesis is a rare congenital anomaly.
- It often presents asymptomatically, but a significant percentage experience biliary colic symptoms.
- Diagnostic challenges arise as ultrasound may misinterpret it as a contracted or scleroatrophic gallbladder.
Observation:
- A 9-year-old child presented with biliary colic.
- Initial ultrasound suggested a scleroatrophic gallbladder, but this was questioned due to the absence of prior cholecystitis.
- Magnetic resonance cholangiopancreatography confirmed the absence of a gallbladder.
Findings:
- Gallbladder agenesis can mimic symptoms of biliary colic.
- Misdiagnosis on ultrasound can lead to unnecessary surgical interventions.
- The absence of gallbladder visualization during imaging warrants consideration of agenesis.
Implications:
- Increased awareness of gallbladder agenesis is crucial for accurate diagnosis.
- Advanced imaging like MRCP aids in confirming the diagnosis.
- Distinguishing agenesis from other gallbladder pathologies prevents inappropriate surgical management and potential complications.
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