Cargando…
Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report
RATIONALE: Acquired neuromyotonia syndrome is a rare form of peripheral nerve hyperexcitability syndrome. It is characterized by spontaneous and continuous muscle contractions. Acquired neuromyotonia syndrome is mainly observed in patients with autoimmune diseases or tumors, but it is a rare neurolo...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360472/ https://www.ncbi.nlm.nih.gov/pubmed/34397926 http://dx.doi.org/10.1097/MD.0000000000026910 |
_version_ | 1783737748794900480 |
---|---|
author | Ran, Enrong Wang, Maohe Yi, Yanxia Feng, Mei Liu, Yuanjun |
author_facet | Ran, Enrong Wang, Maohe Yi, Yanxia Feng, Mei Liu, Yuanjun |
author_sort | Ran, Enrong |
collection | PubMed |
description | RATIONALE: Acquired neuromyotonia syndrome is a rare form of peripheral nerve hyperexcitability syndrome. It is characterized by spontaneous and continuous muscle contractions. Acquired neuromyotonia syndrome is mainly observed in patients with autoimmune diseases or tumors, but it is a rare neurological clinical manifestation in patients with mercury poisoning. PATIENT CONCERNS: A 56-year-old woman presented with continuous and involuntary muscle twitching in her legs for 2 months; it was accompanied by a burning sensation in the lower limbs, insomnia, fatigue, and night sweats. These symptoms did not disappear during sleep. DIAGNOSES: Toxicological blood analysis via atomic fluorescence spectrometry revealed that the level of mercury was 0.07 μmol/L (normal level: <0.05 μmol/L). Her urinary mercury level measured using the cold atomic absorption method was 217.50 μmol/mol creatinine, which was considerably higher than the reference range (0–2.25 μmol/mol creatinine for people not in contact with mercury, 0–20 μmol/mol creatinine following long-term exposure). Upon further testing, a high level of mercury (10,572 mg/kg) was detected in the patient's cream. Accordingly, this patient was diagnosed with mercury poisoning. INTERVENTIONS: Treatment with 2,3-dimercapto-1-propanesulfonic acid (DMPS) was initiated. Her urinary mercury level decreased to 9.67 μmol/mol creatinine, and her neuromyotonia syndrome and hyponatremia were relieved, with urine protein completely disappearing after 3 months of treatment. OUTCOMES: After DMPS treatment, the clinical manifestations of the nervous system disappeared and electrolyte parameters returned to normal levels. LESSONS: Acquired neuromyotonia syndrome is a rare disorder caused by the hyperexcitability of peripheral nerves, resulting in spontaneous and continuous muscle contraction. Mercury poisoning should be considered in patients with neuromyotonia syndrome. Early detection of mercury poisoning can prevent unnecessary examinations and treatments. |
format | Online Article Text |
id | pubmed-8360472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-83604722021-08-17 Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report Ran, Enrong Wang, Maohe Yi, Yanxia Feng, Mei Liu, Yuanjun Medicine (Baltimore) 7200 RATIONALE: Acquired neuromyotonia syndrome is a rare form of peripheral nerve hyperexcitability syndrome. It is characterized by spontaneous and continuous muscle contractions. Acquired neuromyotonia syndrome is mainly observed in patients with autoimmune diseases or tumors, but it is a rare neurological clinical manifestation in patients with mercury poisoning. PATIENT CONCERNS: A 56-year-old woman presented with continuous and involuntary muscle twitching in her legs for 2 months; it was accompanied by a burning sensation in the lower limbs, insomnia, fatigue, and night sweats. These symptoms did not disappear during sleep. DIAGNOSES: Toxicological blood analysis via atomic fluorescence spectrometry revealed that the level of mercury was 0.07 μmol/L (normal level: <0.05 μmol/L). Her urinary mercury level measured using the cold atomic absorption method was 217.50 μmol/mol creatinine, which was considerably higher than the reference range (0–2.25 μmol/mol creatinine for people not in contact with mercury, 0–20 μmol/mol creatinine following long-term exposure). Upon further testing, a high level of mercury (10,572 mg/kg) was detected in the patient's cream. Accordingly, this patient was diagnosed with mercury poisoning. INTERVENTIONS: Treatment with 2,3-dimercapto-1-propanesulfonic acid (DMPS) was initiated. Her urinary mercury level decreased to 9.67 μmol/mol creatinine, and her neuromyotonia syndrome and hyponatremia were relieved, with urine protein completely disappearing after 3 months of treatment. OUTCOMES: After DMPS treatment, the clinical manifestations of the nervous system disappeared and electrolyte parameters returned to normal levels. LESSONS: Acquired neuromyotonia syndrome is a rare disorder caused by the hyperexcitability of peripheral nerves, resulting in spontaneous and continuous muscle contraction. Mercury poisoning should be considered in patients with neuromyotonia syndrome. Early detection of mercury poisoning can prevent unnecessary examinations and treatments. Lippincott Williams & Wilkins 2021-08-13 /pmc/articles/PMC8360472/ /pubmed/34397926 http://dx.doi.org/10.1097/MD.0000000000026910 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 7200 Ran, Enrong Wang, Maohe Yi, Yanxia Feng, Mei Liu, Yuanjun Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report |
title | Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report |
title_full | Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report |
title_fullStr | Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report |
title_full_unstemmed | Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report |
title_short | Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report |
title_sort | mercury poisoning complicated by acquired neuromyotonia syndrome: a case report |
topic | 7200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360472/ https://www.ncbi.nlm.nih.gov/pubmed/34397926 http://dx.doi.org/10.1097/MD.0000000000026910 |
work_keys_str_mv | AT ranenrong mercurypoisoningcomplicatedbyacquiredneuromyotoniasyndromeacasereport AT wangmaohe mercurypoisoningcomplicatedbyacquiredneuromyotoniasyndromeacasereport AT yiyanxia mercurypoisoningcomplicatedbyacquiredneuromyotoniasyndromeacasereport AT fengmei mercurypoisoningcomplicatedbyacquiredneuromyotoniasyndromeacasereport AT liuyuanjun mercurypoisoningcomplicatedbyacquiredneuromyotoniasyndromeacasereport |