Advertisement
Review Article| Volume 38, ISSUE 4, P749-763, November 2020

Toxin-Induced Neuropathies

Published:September 12, 2020DOI:https://doi.org/10.1016/j.ncl.2020.06.002

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribers receive full online access to your subscription and archive of back issues up to and including 2002.

      Content published before 2002 is available via pay-per-view purchase only.

      Subscribe:

      Subscribe to Neurologic Clinics
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Mellion M.
        • Gilchrist J.M.
        • de la Monte S.
        Alcohol-related peripheral neuropathy: nutritional, toxic, or both?.
        Muscle Nerve. 2011; 43: 309-316
        • Substance Abuse and Mental Health Services Administration
        Key substance use and mental health indicators in the United States: results from the 2018 national Survey on drug use and health (HHS publication No. PEP19-5068, NSDUH Series H-54).
        Center for Behavioral Health Statistics and Quality, Substance Abuse and Mental Health Services Administration, Rockville, MD2019 (Available at:)
        • Mellion M.L.
        • Nguyen V.
        • Tong M.
        • et al.
        Experimental model of alcohol-related peripheral neuropathy.
        Muscle Nerve. 2013; 48: 204-211
        • Feldman R.G.
        • Niles C.A.
        • Kelly-Hayes M.
        • et al.
        Peripheral neuropathy in arsenic smelter workers.
        Neurology. 1979; 29: 939-944
        • Trivedi S.
        • Pandit A.
        • Ganguly G.
        • et al.
        Epidemiology of peripheral neuropathy: an Indian perspective.
        Ann Indian Acad Neurol. 2017; 20: 173-184
        • Chakraborti D.
        • Mukherjee S.C.
        • Saha K.C.
        • et al.
        Arsenic toxicity from homeopathic treatment.
        J Toxicol Clin Toxicol. 2003; 41: 963-967
        • Greenberg S.A.
        Acute demyelinating polyneuropathy with arsenic ingestion.
        Muscle Nerve. 1996; 19: 1611-1613
        • Choucair A.K.
        • Ajax E.T.
        Hair and nails in arsenical neuropathy.
        Ann Neurol. 1988; 23: 628-629
        • Kosnett M.J.
        • Wedeen R.P.
        • Rothenberg S.J.
        • et al.
        Recommendations for medical management of adult lead exposure.
        Environ Health Perspect. 2007; 115: 463-471
        • Wu M.L.
        • Deng J.F.
        • Lin K.P.
        • et al.
        Lead, mercury, and arsenic poisoning due to topical use of traditional Chinese medicines.
        Am J Med. 2013; 126: 451-454
        • Little A.A.
        • Albers J.W.
        Clinical description of toxic neuropathies.
        Handb Clin Neurol. 2015; 131: 253-296
        • Franzblau A.
        • d'Arcy H.
        • Ishak M.B.
        • et al.
        Low-level mercury exposure and peripheral nerve function.
        Neurotoxicology. 2012; 33: 299-306
        • Zhao G.
        • Ding M.
        • Zhang B.
        • et al.
        Clinical manifestations and management of acute thallium poisoning.
        Eur Neurol. 2008; 60: 292-297
        • Hoffman R.S.
        • Stringer J.A.
        • Feinberg R.S.
        • et al.
        Comparative efficacy of thallium adsorption by activated charcoal, prussian blue, and sodium polystyrene sulfonate.
        J Toxicol Clin Toxicol. 1999; 37: 833-837
        • Liu C.H.
        • Huang C.Y.
        • Huang C.C.
        Occupational neurotoxic diseases in taiwan.
        Saf Health Work. 2012; 3: 257-267
        • Gottfried M.R.
        • Graham D.G.
        • Morgan M.
        • et al.
        The morphology of carbon disulfide neurotoxicity.
        Neurotoxicology. 1985; 6: 89-96
        • Huang C.C.
        Polyneuropathy induced by n-hexane intoxication in Taiwan.
        Acta Neurol Taiwan. 2008; 17: 3-10
        • Chang A.P.
        • England J.D.
        • Garcia C.A.
        • et al.
        Focal conduction block in n-hexane polyneuropathy.
        Muscle Nerve. 1998; 21: 964-969
        • Misirli H.
        • Domac F.M.
        • Somay G.
        • et al.
        N-hexane induced polyneuropathy: a clinical and electrophysiological follow up.
        Electromyogr Clin Neurophysiol. 2008; 48: 103-108
        • Mowry J.B.
        • Spyker D.A.
        • Cantilena Jr., L.R.
        • et al.
        2012 annual report of the American Association of Poison Control Centers' National Poison Data System (NPDS): 30th Annual Report.
        Clin Toxicol (Phila). 2013; 51: 949-1229
        • Chai P.R.
        • Hayes B.D.
        • Erickson T.B.
        • et al.
        Novichok agents: a historical, current, and toxicological perspective.
        Toxicol Commun. 2018; 2: 45-48
        • Hoffman A.
        • Eisenkraft A.
        • Finkelstein A.
        • et al.
        A decade after the Tokyo sarin attack: a review of neurological follow-up of the victims.
        Mil Med. 2007; 172: 607-610
        • Senanayake N.
        • Karalliedde L.
        Neurotoxic effects of organophosphorus insecticides. An intermediate syndrome.
        N Engl J Med. 1987; 316: 761-763
        • Thompson A.G.
        • Leite M.I.
        • Lunn M.P.
        • et al.
        Whippits, nitrous oxide and the dangers of legal highs.
        Pract Neurol. 2015; 15: 207-209
        • Aoun M.
        • Jacquy C.
        • Debusscher L.
        • et al.
        Peripheral neuropathy associated with fluoroquinolones.
        Lancet. 1992; 340: 127
        • Etminan M.
        • Brophy J.M.
        • Samii A.
        Oral fluoroquinolone use and risk of peripheral neuropathy: a pharmacoepidemiologic study.
        Neurology. 2014; 83: 1261-1263
        • Morales D.
        • Pacurariu A.
        • Slattery J.
        • et al.
        Association between peripheral neuropathy and exposure to oral fluoroquinolone or amoxicillin-clavulanate therapy.
        JAMA Neurol. 2019; 76: 827-833
        • Staff N.P.
        • Dyck P.J.B.
        On the association between fluoroquinolones and neuropathy.
        JAMA Neurol. 2019; 76: 753-754
        • Sanders R.D.
        • Weimann J.
        • Maze M.
        Biologic effects of nitrous oxide: a mechanistic and toxicologic review.
        Anesthesiology. 2008; 109: 707-722
        • Ghavanini A.A.
        • Kimpinski K.
        Revisiting the evidence for neuropathy caused by pyridoxine deficiency and excess.
        J Clin Neuromuscul Dis. 2014; 16: 25-31
        • Leklem J.E.
        Vitamin B-6: a status report.
        J Nutr. 1990; 120 (Suppl 11(4)): 1503-1507
        • Staff N.P.
        • Grisold A.
        • Grisold W.
        • et al.
        Chemotherapy-induced peripheral neuropathy: A current review.
        Ann Neurol. 2017; 81: 772-781
        • Stubgen J.P.
        Lymphoma-associated dysimmune polyneuropathies.
        J Neurol Sci. 2015; 355: 25-36
        • Tomita M.
        • Koike H.
        • Kawagashira Y.
        • et al.
        Clinicopathological features of neuropathy associated with lymphoma.
        Brain. 2013; 136: 2563-2578
        • Bayat E.
        • Kelly J.J.
        Neurological complications in plasma cell dyscrasias.
        Handb Clin Neurol. 2012; 105: 731-746
        • Shin S.C.
        • Robinson-Papp J.
        Amyloid neuropathies.
        Mt Sinai J Med. 2012; 79: 733-748
        • Hershman D.L.
        • Lacchetti C.
        • Dworkin R.H.
        • et al.
        Prevention and management of chemotherapy-induced peripheral neuropathy in survivors of adult cancers: American Society of Clinical Oncology clinical practice guideline.
        J Clin Oncol. 2014; 32: 1941-1967
        • Lee D.
        • Kanzawa-Lee G.
        • Knoerl R.
        • et al.
        Characterization of internal validity threats to phase III clinical trials for chemotherapy-induced peripheral neuropathy management: a systematic review.
        Asia Pac J Oncol Nurs. 2019; 6: 318-332
        • Loprinzi C.
        • Le-Rademacher J.G.
        • Majithia N.
        • et al.
        Scrambler therapy for chemotherapy neuropathy: a randomized phase II pilot trial.
        Support Care Cancer. 2019; 28: 1183-1197
        • Omlin A.
        • Sartor O.
        • Rothermundt C.
        • et al.
        Analysis of side effect profile of alopecia, nail changes, peripheral neuropathy, and dysgeusia in prostate cancer patients treated with docetaxel and cabazitaxel.
        Clin Genitourin Cancer. 2015; 13: e205-e208
        • Reeves B.N.
        • Dakhil S.R.
        • Sloan J.A.
        • et al.
        Further data supporting that paclitaxel-associated acute pain syndrome is associated with development of peripheral neuropathy: North Central Cancer Treatment Group trial N08C1.
        Cancer. 2012; 118: 5171-5178
        • Lavoie Smith E.M.
        • Li L.
        • Chiang C.
        • et al.
        Patterns and severity of vincristine-induced peripheral neuropathy in children with acute lymphoblastic leukemia.
        J Peripher Nerv Syst. 2015; 20: 37-46
        • Atas E.
        • Korkmazer N.
        • Artik H.A.
        • et al.
        Raynaud's phenomenon in a child with medulloblastoma as a late effect of chemotherapy.
        J Cancer Res Ther. 2015; 11: 666
        • Rosenthal S.
        • Kaufman S.
        Vincristine neurotoxicity.
        Ann Intern Med. 1974; 80: 733-737
        • Carlson K.
        • Ocean A.J.
        Peripheral neuropathy with microtubule-targeting agents: occurrence and management approach.
        Clin Breast Cancer. 2011; 11: 73-81
        • Gopal A.K.
        • Ramchandren R.
        • O'Connor O.A.
        • et al.
        Safety and efficacy of brentuximab vedotin for Hodgkin lymphoma recurring after allogeneic stem cell transplantation.
        Blood. 2012; 120: 560-568
        • Krop I.E.
        • Modi S.
        • LoRusso P.M.
        • et al.
        Phase 1b/2a study of trastuzumab emtansine (T-DM1), paclitaxel, and pertuzumab in HER2-positive metastatic breast cancer.
        Breast Cancer Res. 2016; 18: 34
        • Gill J.S.
        • Windebank A.J.
        Cisplatin-induced apoptosis in rat dorsal root ganglion neurons is associated with attempted entry into the cell cycle.
        J Clin Invest. 1998; 101: 2842-2850
        • Johnson C.
        • Pankratz V.S.
        • Velazquez A.I.
        • et al.
        Candidate pathway-based genetic association study of platinum and platinum-taxane related toxicity in a cohort of primary lung cancer patients.
        J Neurol Sci. 2015; 349: 124-128
        • Lehky T.J.
        • Leonard G.D.
        • Wilson R.H.
        • et al.
        Oxaliplatin-induced neurotoxicity: acute hyperexcitability and chronic neuropathy.
        Muscle Nerve. 2004; 29: 387-392
        • Moreau P.
        • Pylypenko H.
        • Grosicki S.
        • et al.
        Subcutaneous versus intravenous bortezomib in patients with relapsed multiple myeloma: subanalysis of patients with renal impairment in the phase III MMY-3021 study.
        Haematologica. 2015; 100: e207-e210
        • Mauermann M.L.
        • Blumenreich M.S.
        • Dispenzieri A.
        • et al.
        A case of peripheral nerve microvasculitis associated with multiple myeloma and bortezomib treatment.
        Muscle Nerve. 2012; 46: 970-977
        • Grover J.K.
        • Uppal G.
        • Raina V.
        The adverse effects of thalidomide in relapsed and refractory patients of multiple myeloma.
        Ann Oncol. 2002; 13: 1636-1640
        • Dalla Torre C.
        • Zambello R.
        • Cacciavillani M.
        • et al.
        Lenalidomide long-term neurotoxicity: Clinical and neurophysiologic prospective study.
        Neurology. 2016; 87: 1161-1166
        • Siegel D.S.
        • Weisel K.C.
        • Dimopoulos M.A.
        • et al.
        Pomalidomide plus low-dose dexamethasone in patients with relapsed/refractory multiple myeloma and moderate renal impairment: a pooled analysis of three clinical trials.
        Leuk Lymphoma. 2016; 57: 2833-2838