A rare clinical presentation of metronidazole-induced dysarthria: A Case report with literature review
Year: 2025
Type: article
Study design: Case Report
Abstract: We described a case of a rare, but notable adverse effect of metronidazole therapy, where a 55-year-old chronic alcoholic patient developed dysarthria following a four-week course of the drug for the treatment of pyogenic liver abscesses. Dysarthria, characterized by slurred or unclear speech, is an uncommon complication of metronidazole, which is generally well-tolerated but has the potential to cause neurotoxic effects in some individuals, especially with prolonged use or high cumulative doses. In this case, the Magnetic Resonance Imaging (MRI) brain revealed T2/FLAIR hyperintensities involving the bilateral dentate nuclei, a key finding associated with metronidazole-induced encephalopathy. The exclusion of other possible causes for dysarthria led to the conclusion that the symptoms were likely induced by metronidazole. This highlights the importance of considering drug-induced neurotoxicity in patients presenting with new neurological symptoms, particularly when there is a history of prolonged antibiotic therapy. The patient's improvement after discontinuing metronidazole and switching to alternative treatment further supports this diagnosis. This case underscores the necessity of closely monitoring patients on metronidazole, especially those receiving prolonged treatment, for any emerging neurological signs. Typical MRI findings play a crucial role in the vigilance for the diagnosis and treatment of such clinical situations. Timely recognition and intervention can help prevent permanent damage and facilitate recovery.
Source: Radiology Case Reports
Authors: Arpan Mitra, Niraj Kumar Srivastava, Ankur Vivek, Nayana Bhuyan, Akansha Jain, Subhraneel Paul, Vijaya Nath Mishra, Abhishek Pathak
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $600
OpenAlex ID: W4408255298
