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Updated: Sep 13, 2025

Nerve Excitability Assessment in Chemotherapy-induced Neurotoxicity
Published on: April 26, 2012
Voriconazole-associated peripheral polyneuropathy: A case report
Bárbara J González1, Paula Ivarola1, Miguel Miranda1
1Neurology Department, Hospital de Pediatría S.A.M.I.C. Prof. Dr. Juan P. Garrahan, Autonomous City of Buenos Aires, Argentina.
Abstract:
Invasive fungal infections, especially aspergillosis, severely affect immunocompromised patients. The use of azoles, particularly voriconazole, has been considered an effective antifungal therapy for the treatment of these infections and prevention. However, cases of peripheral neuropathy have been reported in patients treated with this drug. We present two clinical cases of patients with immunocompromise (acute myeloblastic leukemia and primary immunodeficiency) who, during treatment with voriconazole, developed peripheral sensory motor axonal polyneuropathy, which completely resolved after discontinuation of the medication. Given the rapid resolution of the clinical manifestations after discontinuation of the drug, we consider it essential to keep this neurotoxicity in mind as a differential diagnosis in children exposed to multiple medications.
Insights
Voriconazole, an antifungal, can cause peripheral neuropathy in immunocompromised patients. This neurotoxicity resolved after stopping the drug, highlighting its importance in differential diagnosis.
Area of Science:
- Medical Mycology
- Clinical Neurology
- Pharmacology
Background:
- Invasive fungal infections, particularly aspergillosis, pose a significant threat to immunocompromised individuals.
- Azole antifungals, such as voriconazole, are standard treatments for these infections.
- Voriconazole use has been associated with adverse events, including peripheral neuropathy.
Observation:
- Two cases of immunocompromised patients (acute myeloblastic leukemia and primary immunodeficiency) developed peripheral sensory motor axonal polyneuropathy.
- These neurological symptoms emerged during voriconazole treatment.
- The polyneuropathy completely resolved after voriconazole was discontinued.
Findings:
- Voriconazole can induce peripheral sensory motor axonal polyneuropathy in vulnerable patient populations.
- The neurotoxic effect of voriconazole appears to be reversible upon drug cessation.
- This adverse event warrants consideration in the differential diagnosis of neurological symptoms in patients receiving voriconazole.
Implications:
- Clinicians should consider voriconazole-induced neurotoxicity when evaluating peripheral neuropathy in immunocompromised patients.
- Early recognition and discontinuation of voriconazole may lead to complete recovery from polyneuropathy.
- This finding is particularly relevant for pediatric patients receiving multiple medications, where differentiating drug-induced effects is crucial.
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