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Metronidazole-Induced Hepatitis in a Teenager With Xeroderma Pigmentosum and Trichothiodystrophy Overlap.

Abstract
A teenage girl had the rare combined phenotype of xeroderma pigmentosum and trichothiodystrophy, resulting from mutations in the XPD (ERCC2) gene involved in nucleotide excision repair (NER). After treatment with antibiotics, including metronidazole for recurrent infections, she showed signs of acute and severe hepatotoxicity, which gradually resolved after withdrawal of the treatment. Cultured skin fibroblasts from the patient revealed cellular sensitivity to killing by metronidazole compared with cells from a range of other donors. This reveals that the metronidazole sensitivity was an intrinsic property of her cells. It is well recognized that patients with Cockayne syndrome, another NER disorder, are at high risk of metronidazole-induced hepatotoxicity, but this had not been reported in individuals with other NER disorders. We would urge extreme caution in the use of metronidazole in the management of individuals with the xeroderma pigmentosum and trichothiodystrophy overlap or trichothiodystrophy phenotypes.
AuthorsAdesoji Abiona, Nuno Cordeiro, Heather Fawcett, Deborah Tamura, Sikandar G Khan, John J DiGiovanna, Alan R Lehmann, Hiva Fassihi
JournalPediatrics (Pediatrics) Vol. 148 Issue 4 (10 2021) ISSN: 1098-4275 [Electronic] United States
PMID34593652 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2021 by the American Academy of Pediatrics.
Chemical References
  • Anti-Bacterial Agents
  • Metronidazole
  • Xeroderma Pigmentosum Group D Protein
  • ERCC2 protein, human
Topics
  • Adolescent
  • Anti-Bacterial Agents (adverse effects)
  • Chemical and Drug Induced Liver Injury (etiology)
  • Female
  • Fibroblasts (drug effects)
  • Humans
  • Metronidazole (adverse effects)
  • Mutation
  • Trichothiodystrophy Syndromes (complications, genetics)
  • Xeroderma Pigmentosum (complications, genetics)
  • Xeroderma Pigmentosum Group D Protein (genetics)

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