2.Construction and validation of a nomogram for predicting the risk of secondary peripheral neuropathy in patients with advanced lung cancer.
Journal of Zhejiang University. Medical sciences 2022;51(6):716-723
OBJECTIVE:
To construct and validate a nomogram for predicting the risk of secondary peripheral neuropathy in patients with advanced lung cancer.
METHODS:
The sociodemographic and clinical data of 335 patients with advanced lung cancer admitted to Department of Respiratory, the First Affiliated Hospital of Zhejiang University School of Medicine from May 2020 to May 2021 were retrospectively collected. Pearson correlation analysis, univariate and multivariate logistic regression analyses were used to identify the risk factors of secondary peripheral neuropathy in patients with advanced lung cancer. A nomogram was constructed according to the contribution of each risk factor to secondary peripheral neuropathy, and the receiver operating characteristic (ROC) curve, Calibration curve and clinical decision curve were used to evaluate differentiation, calibration, and the clinical utility of the model. The nomogram was further validated with data from 64 patients with advanced lung cancer admitted between June 2021 and August 2021.
RESULTS:
The incidences of secondary peripheral neuropathy in two series of patients were 34.93% (117/335) and 40.63% (26/64), respectively. The results showed that drinking history ( OR=3.650, 95% CI: 1.523-8.746), comorbid diabetes ( OR=3.753, 95% CI: 1.396-10.086), chemotherapy ( OR=2.887, 95% CI: 1.046-7.970), targeted therapy ( OR=8.671, 95% CI: 4.107-18.306), immunotherapy ( OR=2.603, 95% CI: 1.337-5.065) and abnormal liver and kidney function ( OR=12.409, 95% CI: 4.739-32.489) were independent risk factors for secondary peripheral neuropathy (all P<0.05). A nomogram was constructed based on the above risk factors. The area under the ROC curve (AUC) of the nomogram for predicting the secondary peripheral neuropathy was 0.913 (95% CI: 0.882-0.944); and sensitivity, specificity, positive and negative predictive values were 85.47%, 81.65%, 71.43% and 91.28%, respectively. The Calibration curve and clinical decision curve showed good calibration and clinical utility. External validation results showed that the AUC was 0.764 (95% CI: 0.638-0.869); and sensitivity, specificity, positive and negative predictive values were 79.28%, 85.79%, 73.25% and 85.82%, respectively.
CONCLUSIONS
Advanced lung cancer patients have a high risk of secondary peripheral neuropathy after anticancer therapy. Drinking history, comorbid diabetes, chemotherapy, targeted therapy, immunotherapy, abnormal liver and kidney function are independent risk factors. The nomogram prediction model constructed in the study is effective and may be used for the risk assessment of secondary peripheral neuropathy in patients with advanced lung cancer.
Humans
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Nomograms
;
Retrospective Studies
;
Peripheral Nervous System Diseases/etiology*
;
Risk Factors
;
Lung Neoplasms/complications*
3.Progressive atypical peripheral neuropathy following nephrectomy in a patient with renal cell carcinoma.
Journal of Korean Medical Science 1992;7(2):167-169
Peripheral neuropathy or amyotropic lateral sclerosis can be associated with renal cell carcinoma. We report a 63-year-old male patient with renal cell carcinoma who developed an atypical, progressive neuropathy after nephrectomy.
Carcinoma, Renal Cell/*complications/pathology
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Humans
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Kidney Neoplasms/*complications/pathology
;
Male
;
Middle Aged
;
Nephrectomy
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Peripheral Nervous System Diseases/*etiology
4.A Clinical Study of Peripheral Neuropathy in Carbon Monoxide Intoxication.
Yonsei Medical Journal 1982;23(2):174-177
Twenty cases of peripheral neuropathy as sequelae of carbon monoxide intoxication have been analyzed clinically. The incidence of pheripheral neuropathy was 0.84% in a total of 2,360 cases and 3.64% in 549 admitted cases of carbon monoxide intoxication. The ratio of male to female was 1:1.2 (9:11). Their ages ranged from 17 to 52 years (mean 29.5 years), with a peak incidence in the 3rd decade (55%). The lower extremity was exclusively involved, and the left side was more involved than the right. Symptoms were a burning sensation, tingling sensation, shooting pain and weakness. Other associated sequelae were local swelling, acute renal failure, delayed neurologic sequelae, and Volkman's contracture in that order. Of 20 cases, 6 showed abnormal findings in the electromyogram only, and 14 were abnormal in both electro-myogram and nerve conduction velocity. Fifteen cases recoved within 3 to 6 months.
Adolescent
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Adult
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Carbon Monoxide Poisoning/complications*
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Extremities
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Female
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Human
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Male
;
Middle Age
;
Peripheral Nervous System Diseases/etiology*
6.Electrophysiological study of 16 patients with severe N-hexane neuropathy.
Hong JIANG ; Lei-qian CHEN ; Yue-yu HU
Chinese Journal of Industrial Hygiene and Occupational Diseases 2005;23(5):351-354
OBJECTIVETo observe electrophysiological changes of severe N-hexane neuropathy getting active therapies and discuss its prognosis.
METHODSA follow-up study involved 16 adult severe N-hexane neuropathy patients who got active therapies was performed. EMG in right muscle of thenar, tibial muscle, and vastus medialis, NCV in right median nerve, common peroneal nerve, and sural nerve were determined and analyzed before treatment and in the first, the third, the ninth, and the twenty-fourth month after treatment.
RESULTSThe electrophysiology in severe N-hexane neuropathy patients showed that the voluntary potential during muscle relaxation increased by 25.0%; the motor unit potential time limit prolonged by 20.8%, and the amplitude increased by 12.5%, and multiphasic wave increased by 16.5% during mild contraction; the raise decreased by 25.0% during strong contraction. In control group, the MCV, SCV, SNAP, DML, and CMAP of median nerve were (54.63 +/- 5.33) m/s, (59.25 +/- 6.45) m/s, (26.53 +/- 6.32) microV, (3.96 +/- 0.65)ms, and (9.89 +/- 2.30) mV respectively, the MCV, CMAP, DML of common peroneal nerve were (48.49 +/- 3.25) m/s, (5.47 +/- 1.77) mV, (5.20 +/- 1.27) ms respectively, and the SCV, SNAP of sural nerve were (63.21 +/- 9.30) m/s, (4.63 +/- 1.29) microV respectively. Severe N-hexane neuropathy patients presented significantly different abnormalities in the NCV and EMG (P < 0.01). The MCV, SCV, SNAP, DML, CMAP of median nerve were (46.00 +/- 4.32) m/s, (40.66 +/- 2.65) m/s, (7.98 +/- 1.05) microV, (4.28 +/- 0.63) ms, and (6.32 +/- 1.54) mV respectively. The MCV, CMAP, DML of common peroneal nerve were (48.49 +/- 3.25) m/s, (3.21 +/- 1.99) mV, (7.32 +/- 1.65) ms respectively. The SCV, SNAP of sural nerve were (36.48 +/- 5.20) m/s, (2.15 +/- 1.22) microV respectively. These parameters gradually recovered to normal levels in 24 months after treatment.
CONCLUSIONThe electrophysiological abnormalities in severe N-hexane neuropathy patients can restore after treatment, and clinical prognosis is good.
Adult ; Case-Control Studies ; Electromyography ; Female ; Hexanes ; poisoning ; Humans ; Neural Conduction ; Occupational Exposure ; Peripheral Nervous System Diseases ; etiology ; physiopathology
7.Peripheral neuropathy as a hypereosinophilic syndrome and anti-GM1 antibodies.
Geun Ho LEE ; Kwang Woo LEE ; Je Geun CHI
Journal of Korean Medical Science 1993;8(3):225-229
The acute peripheral neuropathy as one of hypereosinophilic syndrome is known to be a rare disorder. The authors experienced a dramatic case with acute peripheral neuropathy, hypereosinophilia in peripheral blood, and the positive anti-GM1 antibodies. The serum protein electrophoresis showed a diffusely increased gamma-globulin region and the polyclonal gammopathy was found by the immunoelectropheresis. There was no evidence of inflammatory myopathy in vastus lateralis muscle. The sural nerve biopsy was compatible with vascular neuropathy, as there were a few myelin digestion chambers, mild perineuronal fibrosis, and perivascular lymphoplasmocytic infiltration with focal organizing thrombosis. The clinical response to prednisone therapy was excellent.
Acute Disease
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Adult
;
Antibodies/*blood
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G(M1) Ganglioside/*immunology
;
Humans
;
Hypereosinophilic Syndrome/*complications/immunology
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Male
;
Peripheral Nervous System Diseases/*etiology
8.Clinical and genetic analysis of a patient with Krabbe disease presented as peripheral neuropathy.
Wei WANG ; Yali QIN ; Renbin WANG ; Weihe ZHANG ; Linwei ZHANG ; Lei CUI ; Ming JIN ; Yujuan JIAO ; Jingsong JIAO
Chinese Journal of Medical Genetics 2019;36(8):821-825
OBJECTIVE:
To explore the clinical, electrophysiological and imaging features of a patient with Krabbe disease caused by GALC mutation.
METHODS:
A comprehensive analysis including clinical investigation and genetic testing was carried out.
RESULTS:
The patient presented with peripheral neuropathy with electrophysiological anomaly suggestive of asymmetric demyelinating neuropathy. Brain imaging revealed leukoencephalopathy. Genetic analysis has identified compound heterozygous mutations in exons 5 and 11 of the GALC gene, namely c.461C>A and c.1244G>A.
CONCLUSION
Krabbe disease is a group of disorders featuring substantial phenotypic heterogeneity. Genetic and enzyme testing has become indispensable for accurate diagnosis for this disease.
DNA Mutational Analysis
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Galactosylceramidase
;
genetics
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Genetic Testing
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Humans
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Leukodystrophy, Globoid Cell
;
complications
;
genetics
;
Mutation
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Peripheral Nervous System Diseases
;
etiology
9.Occupational Neurological Disorders in Korea.
Journal of Korean Medical Science 2010;25(Suppl):S26-S35
The purpose of this article was to provide a literature review of occupational neurological disorders and related research in Korea, focusing on chemical hazards. We reviewed occupational neurological disorders investigated by the Occupational Safety and Health Research Institute of Korean Occupational Safety and Health Agency between 1992 and 2009, categorizing them as neurological disorders of the central nervous system (CNS), of the peripheral nervous system (PNS) or as neurodegenerative disorders. We also examined peer-reviewed journal articles related to neurotoxicology, published from 1984 to 2009. Outbreaks of occupational neurological disorder of the CNS due to inorganic mercury and carbon disulfide poisoning had helped prompt the development of the occupational safety and health system of Korea. Other major neurological disorders of the CNS included methyl bromide intoxication and chronic toxic encephalopathy. Most of the PNS disorders were n-hexane-induced peripheral neuritis, reported from the electronics industry. Reports of manganese-induced Parkinsonism resulted in the introduction of neuroimaging techniques to occupational medicine. Since the late 1990s, the direction of research has been moving toward degenerative disorder and early effect of neurotoxicity. To understand the early effects of neurotoxic chemicals in the preclinical stage, more follow-up studies of a longer duration are necessary.
Adolescent
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Adult
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Central Nervous System Diseases/chemically induced/epidemiology
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Female
;
Humans
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Male
;
Middle Aged
;
Nervous System Diseases/chemically induced/*epidemiology/etiology
;
Neurodegenerative Diseases/chemically induced/epidemiology
;
Neurotoxicity Syndromes/*epidemiology/*etiology
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Occupational Diseases/chemically induced/*epidemiology/etiology
;
Parkinsonian Disorders/chemically induced/epidemiology
;
Peripheral Nervous System Diseases/chemically induced/epidemiology
;
Republic of Korea
10.Progress of peripheral nerve repair.
Chinese Journal of Traumatology 2002;5(6):323-325
Study on repair of peripheral nerve injury has been proceeding over a long period of time. With the use of microsurgery technique since 1960s the quality of nerve repair has been greatly improved. In the past 40 years, with the continuous increase of surgical repair methods, more progress has been made on the basic research of peripheral nerve repair.
Female
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Humans
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Injury Severity Score
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Male
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Microsurgery
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methods
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Nerve Regeneration
;
physiology
;
Neurosurgical Procedures
;
methods
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Peripheral Nerve Injuries
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Peripheral Nerves
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surgery
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Peripheral Nervous System Diseases
;
etiology
;
surgery
;
Prognosis
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Recovery of Function
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Treatment Outcome