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Induction of Drug-Induced, Autoimmune Hepatitis in BALB/c Mice for the Study of Its Pathogenic Mechanisms
Published on: May 29, 2020
Cholestatic hepatitis with severe systemic reactions induced by trimethoprim-sulfamethoxazole
G Kouklakis1, A Mpoumponaris, P Zezos
1Gastroenterology and Hepatology Department, 424 Army Hospital, Thessaloniki, Greece.
Abstract:
Trimethoprim-Sulfomethoxazole (TMP-SMX) related hepatotoxicity and associated severe systemic reaction are not frequent and documented only in case reports. We report a case of a 30-year-old man, who underwent a 15-day therapy with TMP-SMX for urinary tract infection and two weeks later developed acute cholestatic hepatitis, fever and a skin rash followed by severe systemic reaction. He was admitted in Intensive Care unit and with supportive therapy and prednisolone administration, he showed subsequent improvement over a period of few days. He had fully recovered months later. All tests for other causes of liver disease were negative and his liver biopsy showed evidence of drug-induced hepatic injury.
Insights
Trimethoprim-Sulfamethoxazole (TMP-SMX) can cause rare but severe liver injury and systemic reactions. Prompt supportive care and corticosteroids aided recovery in a patient with drug-induced cholestatic hepatitis.
Area of Science:
- Hepatology
- Pharmacology
- Toxicology
Background:
- Trimethoprim-Sulfamethoxazole (TMP-SMX) is a common antibiotic.
- Hepatotoxicity and severe systemic reactions are infrequent but serious adverse effects.
Observation:
- A 30-year-old man developed acute cholestatic hepatitis, fever, and rash two weeks after a 15-day TMP-SMX course for a urinary tract infection.
- Symptoms progressed to a severe systemic reaction, necessitating intensive care unit admission.
Findings:
- The patient improved with supportive therapy and prednisolone.
- Liver biopsy confirmed drug-induced hepatic injury, with other causes ruled out.
Implications:
- This case highlights the potential for severe hepatotoxicity from TMP-SMX.
- Early recognition and management are crucial for favorable outcomes in drug-induced liver injury.
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