Evidence map›Paper›PMID 42016615›Full record

ArticleClinical case reports2026

Vincristine-Induced Unilateral Foot Drop in a Patient With Diffuse Large B-Cell Lymphoma: A Rare Presentation of Severe Motor Axonopathy.

Nishchal Regmi, Prashant Pant, Umang Gupta, Mipsang Lama

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Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nishchal RegmiDepartment of Internal Medicine Patan Academy of Health Sciences Lalitpur Nepal.ORCID https://orcid.org/0009-0009-4965-1246
Prashant PantDepartment of Internal Medicine Patan Academy of Health Sciences Lalitpur Nepal.
Umang GuptaPalisades Medical Center Hackensack Meridian Health North Bergen New Jersey USA.
Mipsang LamaDepartment of Hematology Patan Academy of Health Sciences Lalitpur Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vincristine is a cornerstone chemotherapeutic agent in combination regimens for lymphoid malignancies; however, its neurotoxicity remains a major dose-limiting adverse effect. While vincristine-induced peripheral neuropathy (VIPN) commonly presents as a symmetric, sensory-predominant polyneuropathy, isolated unilateral motor neuropathy causing foot drop is exceedingly rare. We report a case of a 64-year-old male with extranodal diffuse large B-cell lymphoma (DLBCL) of the left calf muscle, staged as Ann Arbor stage IE with Revised International Prognostic Index (R-IPI) score of 2, who developed left-sided foot drop following the second cycle of dose-adjusted R-DA-EPOCH chemotherapy. Neurological examination confirmed isolated left peroneal nerve palsy with mild sensory involvement, and nerve conduction studies revealed motor axonal neuropathy consistent with vincristine toxicity. MRI excluded local compressive or infiltrative pathology and demonstrated interval tumor response. Vincristine dosing did not exceed the capped dose of 2 mg during the first two cycles; from the third cycle onward, the dose was reduced by approximately 60%. Early physiotherapy, ankle-foot orthosis support, and symptomatic pharmacologic therapy were initiated, leading to gradual neurological recovery. This case highlights the importance of early recognition of vincristine-induced neuropathy and timely dose adjustment to prevent irreversible deficits while maintaining therapeutic efficacy.

Indexed as

chemotherapy‐induced neurotoxicitydiffuse large B‐cell lymphomafoot dropmotor axonopathyvincristine

Identifiers

PMID42016615
PMCPMC13093541

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