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Published Online, 21 September 2004, www.theannals.com, DOI 10.1345/aph.1E162.
The Annals of Pharmacotherapy: Vol. 38, No. 11, pp. 1844-1847. DOI 10.1345/aph.1E162
© 2004 Harvey Whitney Books Company.
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Recurrent Acute Hepatitis Associated with Use of Cetirizine

Maurizio Pompili, MD

Assistant Professor of Internal Medicine, Department of Internal Medicine, Università Cattolica del Sacro Cuore, Rome, Italy

Maria Basso, MD

Resident in Internal Medicine, Department of Internal Medicine, Università Cattolica del Sacro Cuore

Antonio Grieco, MD

Associate Professor of Internal Medicine, Department of Internal Medicine, Università Cattolica del Sacro Cuore

Fabio M Vecchio, MD

Associate Professor of Pathology, Department of Pathology, Università Cattolica del Sacro Cuore

Giovanni Gasbarrini, MD

Professor of Internal Medicine, Department of Internal Medicine, Università Cattolica del Sacro Cuore

Gian Ludovico Rapaccini, MD

Associate Professor of Internal Medicine, Department of Internal Medicine, Università Cattolica del Sacro Cuore

Reprints: Maurizio Pompili MD, Istituto di Medicina Interna e Geriatria, Università Cattolica del Sacro Cuore, Largo A. Gemelli, 8 - 00168 Roma, Italy, fax 0635502775, mpompili{at}rm.unicatt.it

OBJECTIVE: To describe a case of recurrent acute hepatitis related to the use of cetirizine, a selective histamine1-receptor antagonist approved for the treatment of common allergic diseases.

CASE SUMMARY: A 26-year-old man was hospitalized with a week-long history of weakness, nausea, anorexia, and hyperchromic urine, which had developed after 6 days of therapy with oral cetirizine 10 mg/day for allergic rhinitis. Admission laboratory testing revealed evidence of acute hepatitis and seropositivity for liver–kidney microsome antibodies. Liver biopsy findings of diffuse portal tract and lobular inflammation with a prominent eosinophilic infiltrate were consistent with drug-related hepatitis. The patient was discharged after one week of treatment with tocopherol and glutathione. Three months after discharge, transaminase levels were normal. At 6 months, seropositivity for liver–kidney microsome antibodies was still present, but considerably less intense. The patient had suffered 2 previous episodes of "acute hepatitis of unknown origin," and both had occurred after cetirizine use.

DISCUSSION: Use of the Naranjo probability scale indicated cetirizine as the probable cause of acute hepatitis, and the positivity for liver–kidney microsome antibodies is suggestive of an autoimmune mechanism for liver damage. As of September 13, 2004, ours is the fourth reported case of acute hepatitis associated with cetirizine and the second in which liver–kidney microsome antibodies have been documented.

CONCLUSIONS: Although cetirizine is considered to have low potential for severe hepatic toxicity, the possibility that it can provoke autoimmune-mediated hepatotoxicity should be considered.

Key Words: acute hepatitis, cetirizine

Published Online, September 21, 2004. www.theannals.com, DOI 10.1345/aph.1E162





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