Korean J Med.  2008 Nov;75(5):564-568.

A case of acute drug-induced hepatotoxicity after albendazole treatment

Affiliations
  • 1Department of Internal Medicine, Kangdong Sacred Heart Hospital, College of Medicine Hallym University, Seoul, Korea. mkjang2@medimail.co.kr
  • 2Department of Pathology, Kangdong Sacred Heart Hospital, College of Medicine Hallym University, Seoul, Korea.

Abstract

Drug-induced hepatotoxicity is injury to the liver as a result of drug exposure. Due to their unpredictable nature, drug-induced liver injuries pose a serious problem for clinicians, health agencies, and pharmaceutical firms. Albendazole is a benzimidazole with wide spectrum coverage as an antiparasitic drug. Very few cases of high-dose albendazole-induced hepatotoxicity have been reported so far, and no case in response to a single dose. A 25-year-old man presented to our hospital with dark urine. Twenty days prior to presentation, he took a tablet of albendazole (400 mg) as a prophylactic treatment for lumbricosis. Upon laboratory analysis, aspartate aminotransferase (AST) was 748 IU/L, alanine transaminase (ALT) was 939 IU/L, and total/direct bilirubin was 9.3/7.3 mg/dL. The patient was negative for viral markers (HAV, HBV, and HCV) and autoantibodies. Abdominal ultrasonography revealed no evidence of chronic liver damage. The pathology was compatible with drug-induced hepatotoxicity. The patient improved with conservative management only.

Keyword

Albendazole; Hepatotoxicity

MeSH Terms

Adult
Alanine Transaminase
Albendazole
Aspartate Aminotransferases
Autoantibodies
Benzimidazoles
Bilirubin
Biomarkers
Drug-Induced Liver Injury
Humans
Liver
Alanine Transaminase
Albendazole
Aspartate Aminotransferases
Autoantibodies
Benzimidazoles
Bilirubin
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