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Published on: August 23, 2022
Gallbladder Agenesis without Additional Biliary Tracts Abnormality.
Seyed Mostafa Meshkati Yazd1, Hamidreza Bayati2, Sara Sadat Nabavizadeh3
1Department of Surgery, Tehran University of Medical Sciences, Tehran, Iran.
Gallbladder agenesis (GA), a rare biliary disorder, can be challenging to diagnose preoperatively. This case report details an intraoperative discovery of GA, leading to successful symptom management and highlighting the need for surgeon awareness.
Area of Science:
- Gastroenterology
- Surgical Diagnosis
- Biliary System Anatomy
Background:
- Gallbladder agenesis (GA) is an uncommon congenital anomaly of the biliary system.
- Accurate preoperative diagnosis of GA can be challenging, potentially leading to unnecessary surgical interventions.
- This case report focuses on the intraoperative diagnosis and effective management of GA.
Observation:
- A 46-year-old woman presented with symptoms suggestive of chronic cholecystitis, including abdominal pain, nausea, and vomiting.
- Laparoscopic surgery revealed the absence of a gallbladder, leading to an intraoperative diagnosis of GA.
- The patient subsequently underwent MRCP and ERCP with sphincterotomy for symptom relief.
Findings:
- Intraoperative identification of gallbladder agenesis.
- Successful management of symptoms through ERCP and sphincterotomy.
- Patient remained symptom-free one year post-procedure.
Implications:
- Highlights the importance of considering GA in the differential diagnosis for patients with biliary symptoms.
- Emphasizes the need for surgeon preparedness to avoid unnecessary procedures when encountering unexpected findings like GA.
- Suggests that ERCP and sphincterotomy can be effective in managing symptoms associated with GA.
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