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Agenesis of the gallbladder: A multicenter case series and review of the bibliography
Guillermo Costaguta1, Alejandro Costaguta2, Fernando Álvarez1,3
1Department of Pediatric Gastroenterology, Hepatology, and Nutrition, CHU Mère-enfant Sainte-Justine de Montréal, Montreal, Canada.
Insights
Gallbladder agenesis, a rare pediatric condition, often presents diagnostic challenges. Early diagnosis enables effective medical treatment and identifies associated malformations for specialized care.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Medical Diagnostics
Background:
- Gallbladder agenesis is a rare congenital anomaly.
- It often presents asymptomatically, posing diagnostic difficulties.
- Symptoms can mimic other biliary tract diseases, leading to misdiagnosis and unnecessary surgery.
Abstract:
Gallbladder agenesis is a rare condition in pediatrics that is usually asymptomatic and represents a diagnostic challenge for physicians seeing these cases for the first time. Some patients may, however, present with symptoms that mimic other diseases of the bile ducts, and many of them undergo surgery due to such suspicion. Still, a timely diagnosis of gallbladder agenesis allows for medical treatment that is often sufficient to resolve the patient's problem. Although it is a benign condition, patients often present with other associated, more serious malformations and should be actively studied for a timely referral to other specialists. Here we describe our experience with the diagnosis and treatment of these patients and a brief review of the bibliography. We hope it will be helpful for physicians facing similar cases.
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