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Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report
RATIONALE: Whereas metronidazole-induced hepatotoxicity is quite rare in the general population, in individuals carrying a nucleotide excision repair disorder, namely Cockayne syndrome, there is a high risk of developing this complication. PATIENT CONCERNS: We report the case of a 44-year-old man, a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276075/ https://www.ncbi.nlm.nih.gov/pubmed/35623073 http://dx.doi.org/10.1097/MD.0000000000029416 |
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author | Vanoli, Jennifer Nava, Miriam Invernizzi, Chiara Panizzuti, Fabio Grassi, Guido |
author_facet | Vanoli, Jennifer Nava, Miriam Invernizzi, Chiara Panizzuti, Fabio Grassi, Guido |
author_sort | Vanoli, Jennifer |
collection | PubMed |
description | RATIONALE: Whereas metronidazole-induced hepatotoxicity is quite rare in the general population, in individuals carrying a nucleotide excision repair disorder, namely Cockayne syndrome, there is a high risk of developing this complication. PATIENT CONCERNS: We report the case of a 44-year-old man, affected by xeroderma pigmentosum, who was admitted to the hospital presenting aspiration pneumoniae caused by worsening dysphagia and with severe hepatotoxicity during the hospitalization. DIAGNOSES: Acute hepatitis, which was leading to acute liver failure, occurred during antibiotic treatment with metronidazole and ceftazidime with an elevation of liver enzymes consistent with hepatocellular damage pattern. INTERVENTIONS: Hydration with glucose 5% solution, pantoprazole and vitamin K were administered, meanwhile other causes of hepatitis were ruled out and the ongoing antibiotic treatment was stopped suspecting a drug-induced liver injury. OUTCOMES: Liver function nearly completely recovered 1 month later with a first rapid improvement, within few days, of aminotransferases and coagulation studies, and slower of cholestatic enzymes. LESSONS: We describe the first case available in the literature of hepatotoxicity associated with metronidazole treatment in a xeroderma pigmentosum patient. Clinicians therefore, based on this report and according to the possible underlying mechanism shared by other genetic diseases characterized by alterations in the pathway of DNA-repair, should consider such adverse event also in patients affected by this rare disease. |
format | Online Article Text |
id | pubmed-9276075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-92760752022-07-13 Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report Vanoli, Jennifer Nava, Miriam Invernizzi, Chiara Panizzuti, Fabio Grassi, Guido Medicine (Baltimore) 4500 RATIONALE: Whereas metronidazole-induced hepatotoxicity is quite rare in the general population, in individuals carrying a nucleotide excision repair disorder, namely Cockayne syndrome, there is a high risk of developing this complication. PATIENT CONCERNS: We report the case of a 44-year-old man, affected by xeroderma pigmentosum, who was admitted to the hospital presenting aspiration pneumoniae caused by worsening dysphagia and with severe hepatotoxicity during the hospitalization. DIAGNOSES: Acute hepatitis, which was leading to acute liver failure, occurred during antibiotic treatment with metronidazole and ceftazidime with an elevation of liver enzymes consistent with hepatocellular damage pattern. INTERVENTIONS: Hydration with glucose 5% solution, pantoprazole and vitamin K were administered, meanwhile other causes of hepatitis were ruled out and the ongoing antibiotic treatment was stopped suspecting a drug-induced liver injury. OUTCOMES: Liver function nearly completely recovered 1 month later with a first rapid improvement, within few days, of aminotransferases and coagulation studies, and slower of cholestatic enzymes. LESSONS: We describe the first case available in the literature of hepatotoxicity associated with metronidazole treatment in a xeroderma pigmentosum patient. Clinicians therefore, based on this report and according to the possible underlying mechanism shared by other genetic diseases characterized by alterations in the pathway of DNA-repair, should consider such adverse event also in patients affected by this rare disease. Lippincott Williams & Wilkins 2022-05-27 /pmc/articles/PMC9276075/ /pubmed/35623073 http://dx.doi.org/10.1097/MD.0000000000029416 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 4500 Vanoli, Jennifer Nava, Miriam Invernizzi, Chiara Panizzuti, Fabio Grassi, Guido Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report |
title | Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report |
title_full | Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report |
title_fullStr | Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report |
title_full_unstemmed | Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report |
title_short | Metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: A case report |
title_sort | metronidazole-induced hepatotoxicity in a patient with xeroderma pigmentosum: a case report |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276075/ https://www.ncbi.nlm.nih.gov/pubmed/35623073 http://dx.doi.org/10.1097/MD.0000000000029416 |
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