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[Multifocal biliary papillomatosis: an indication for liver transplantation]
M A Ciardullo1, J Pekolj, J E Acuña Barrios
1Servicio de cirurgia, hospital italiano, Buenos Aires, Argentine.
Biliary papillomatosis is a rare condition. Liver transplantation effectively treated a patient with diffuse bilobar biliary papillomatosis, resolving complications like cholangitis and cholestasis.
Area of Science:
- Gastroenterology and Hepatology
- Surgical Oncology
Background:
- Biliary papillomatosis is an uncommon biliary tract disease.
- High recurrence rates and malignant transformation potential necessitate aggressive treatment.
- Orthotopic liver transplantation is a potential curative option.
Observation:
- A 60-year-old patient presented with diffuse bilobar biliary papillomatosis.
- Complications included cholangitis, cholestasis, portal hypertension (esophageal varices, hypersplenism), and hydroelectrolytic imbalance from external biliary drainage.
- Endoscopic retrograde cholangiopancreatography (ERCP) with biopsies confirmed the diagnosis.
Findings:
- The patient underwent successful orthotopic liver transplantation.
- Postoperative recovery was uncomplicated.
- At 9 months post-transplant, the patient was asymptomatic with a satisfactory clinical evolution.
Implications:
- Liver transplantation offers a viable treatment for complex biliary papillomatosis.
- This case highlights the successful management of a rare condition with significant complications.
- Further research into alternative and adjunctive therapies is warranted.
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