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Published on: February 10, 2015
Mycophenolate mofetil for drug-induced vanishing bile duct syndrome
S-Simona Jakab1, A-Brian West, Dennis-M Meighan
1Norwalk Hospital, Section of Gastroenterology, 24 Stevens Street, Norwalk, CT 06856, United States.
Abstract:
Amoxicillin/clavulanate is associated with liver injury, mostly of a cholestatic pattern. While outcomes are usually benign, progression to cirrhosis and death has been reported. The role of immunosuppressive therapy for patients with a protracted course is unclear. We report the case of an elderly patient who developed prolonged cholestasis secondary to amoxicillin/clavulanate. Vanishing bile duct syndrome was confirmed by sequential liver biopsies. The patient responded to prednisone treatment, but could not be weaned off corticosteroids, even when azathioprine was added. Complete withdrawal of both prednisone and azathioprine was possible by using mycophenolate mofetil, an inosine monophosphate dehydrogenase inhibitor. Sustained remission has been maintained for more than 3 years with low-dose mycophenolate mofetil.
Insights
Amoxicillin/clavulanate can cause prolonged liver injury. Mycophenolate mofetil effectively treated a patient with vanishing bile duct syndrome, allowing corticosteroid withdrawal.
Area of Science:
- Hepatology
- Clinical Pharmacology
Background:
- Amoxicillin/clavulanate is a common cause of drug-induced liver injury, typically cholestatic.
- While often self-limiting, severe or protracted cases can occur, necessitating treatment considerations.
Observation:
- An elderly patient presented with prolonged cholestasis following amoxicillin/clavulanate use.
- Liver biopsies confirmed vanishing bile duct syndrome, a severe form of cholestatic liver injury.
Findings:
- Initial treatment with prednisone provided partial response but failed to allow corticosteroid weaning.
- Addition of azathioprine did not facilitate corticosteroid withdrawal.
- Mycophenolate mofetil, an inosine monophosphate dehydrogenase inhibitor, enabled complete withdrawal of prednisone and azathioprine.
Implications:
- This case highlights mycophenolate mofetil as a potential therapeutic option for refractory drug-induced vanishing bile duct syndrome.
- It suggests a role for immunosuppressive therapy in managing severe, protracted cholestatic liver injury from amoxicillin/clavulanate.
- Further research is warranted to explore the efficacy and safety of mycophenolate mofetil in similar cases.
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