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Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis

Nitrous oxide (N(2)O), commonly known as laughing gas, is widely used in clinical practice and food industry. However, an increasing number of young people have been abusing N(2)O for recreational purpose, resulting in many functional disorders and sometimes irreversible nerve damage. We present the...

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Autores principales: Dong, Mei-Xue, Wang, Qing, Xu, Jun-Feng, Hu, Ling, Yu, Ying, Li, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702802/
https://www.ncbi.nlm.nih.gov/pubmed/36452172
http://dx.doi.org/10.3389/fneur.2022.1033327
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author Dong, Mei-Xue
Wang, Qing
Xu, Jun-Feng
Hu, Ling
Yu, Ying
Li, Tao
author_facet Dong, Mei-Xue
Wang, Qing
Xu, Jun-Feng
Hu, Ling
Yu, Ying
Li, Tao
author_sort Dong, Mei-Xue
collection PubMed
description Nitrous oxide (N(2)O), commonly known as laughing gas, is widely used in clinical practice and food industry. However, an increasing number of young people have been abusing N(2)O for recreational purpose, resulting in many functional disorders and sometimes irreversible nerve damage. We present the case of a 20-year-old N(2)O abuser who gradually developed peripheral neuropathy after continuously inhaling N(2)O for 2 months. The neurological symptoms of the patient had kept exacerbation for the next 2 months until she came for medical care sitting in a wheelchair. We suggested the patient halting N(2)O intake and supplementing methylcobalamine according to the standardized protocol. Her symptoms had partly recovered during the following 2 weeks but remained unchanged in another 2 weeks. Antibodies against ganglioside complexes were detected and anti-GM1 IgM antibodies were positive in both cerebrospinal fluid and serum. Intravenous immunoglobulin was given as an additional treatment and the patient's symptoms had significantly recovered further. The patient discharged walking by herself. Then she has been continuously followed up in outpatient department for the next 4 months and taking steroid hormone as well as methylcobalamine. Her symptoms gradually disappeared and all the electrophysiological parameters significantly improved. With this case we were able to show that N(2)O-related peripheral neuropathy is not only a metabolic disorder but also an immune-mediated disease. N(2)O intake can trigger a mimic Guillain-Barré syndrome.
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spelling pubmed-97028022022-11-29 Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis Dong, Mei-Xue Wang, Qing Xu, Jun-Feng Hu, Ling Yu, Ying Li, Tao Front Neurol Neurology Nitrous oxide (N(2)O), commonly known as laughing gas, is widely used in clinical practice and food industry. However, an increasing number of young people have been abusing N(2)O for recreational purpose, resulting in many functional disorders and sometimes irreversible nerve damage. We present the case of a 20-year-old N(2)O abuser who gradually developed peripheral neuropathy after continuously inhaling N(2)O for 2 months. The neurological symptoms of the patient had kept exacerbation for the next 2 months until she came for medical care sitting in a wheelchair. We suggested the patient halting N(2)O intake and supplementing methylcobalamine according to the standardized protocol. Her symptoms had partly recovered during the following 2 weeks but remained unchanged in another 2 weeks. Antibodies against ganglioside complexes were detected and anti-GM1 IgM antibodies were positive in both cerebrospinal fluid and serum. Intravenous immunoglobulin was given as an additional treatment and the patient's symptoms had significantly recovered further. The patient discharged walking by herself. Then she has been continuously followed up in outpatient department for the next 4 months and taking steroid hormone as well as methylcobalamine. Her symptoms gradually disappeared and all the electrophysiological parameters significantly improved. With this case we were able to show that N(2)O-related peripheral neuropathy is not only a metabolic disorder but also an immune-mediated disease. N(2)O intake can trigger a mimic Guillain-Barré syndrome. Frontiers Media S.A. 2022-11-14 /pmc/articles/PMC9702802/ /pubmed/36452172 http://dx.doi.org/10.3389/fneur.2022.1033327 Text en Copyright © 2022 Dong, Wang, Xu, Hu, Yu and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Dong, Mei-Xue
Wang, Qing
Xu, Jun-Feng
Hu, Ling
Yu, Ying
Li, Tao
Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
title Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
title_full Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
title_fullStr Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
title_full_unstemmed Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
title_short Case report: Recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
title_sort case report: recreational nitrous oxide abuse triggered peripheral neuropathy possibly through the immune-mediated pathogenesis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702802/
https://www.ncbi.nlm.nih.gov/pubmed/36452172
http://dx.doi.org/10.3389/fneur.2022.1033327
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