汞暴露导致功能性维生素B12缺乏和亚急性合并变性:一例报告和文献复习。

IF 4.6 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2025-09-09 eCollection Date: 2025-01-01 DOI:10.3389/ftox.2025.1580275
Isidora Semnic, Valentino Rački, Olivia Perković, Vladimira Vuletić
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引用次数: 0

摘要

文献中已经报道了神经症状学与重金属暴露之间的关系。少数病例的锥体外系症状和亚急性合并变性已被描述为汞中毒的表现。我们报告一例患者表现为帕金森特征(震颤、强直和运动迟缓)、锥体缺陷、构音障碍、感觉异常、轻度认知衰退和情绪不稳定,血液和头发中汞含量升高,尿液中砷含量升高。病例:一名60岁男性,在废物管理和环境保护中心工作时有汞接触史,在持续震颤、肌肉痉挛、感觉异常和烦躁10个月后,出现运动迟缓、言语不清、僵硬、失眠和轻微认知能力下降。实验室调查显示功能性维生素B12和维生素D缺乏,而毒理学定量分析显示血汞水平升高(15.2 μg/L),发根水平升高(3 μg/g)。脑部MRI检查正常,而后颈椎MRI检查发现脊髓病征象。脑氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)显示双侧颞叶和顶叶葡萄糖代谢低下,最明显的是左侧顶叶下区和左侧颞上区。单光子发射计算机断层扫描(SPECT)显示纹状体多巴胺能神经元为阴性,患者对左旋多巴无反应。多种维生素治疗(维生素B、E和D)加硒,结合对症治疗(苯二氮卓类药物、肌肉松弛剂和抗抑郁药)提供了最小程度的缓解,导致引入n -乙酰半胱氨酸,导致症状适度改善。在这种情况下,物理和语言治疗非常重要。讨论:该病例是独特的,因为它代表了汞暴露3年以上治疗抵抗性锥体外系症状的发展,可能导致功能性维生素B12缺乏症引起的亚急性合并变性。流行病学资料描述了甲基汞中毒,即所谓的水俣病,其表现为躯体感觉缺陷、共济失调、帕金森病、构音障碍以及视觉和听力障碍。结论:对于出现不明原因、左旋多巴抵抗性锥体外系症状、行为和睡眠障碍、认知能力下降和其他非特异性神经症状的患者,应考虑进行血液和尿液重金属毒理学筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mercury exposure leading to functional vitamin B12 deficiency and subacute combined degeneration: a case report and literature review.

Mercury exposure leading to functional vitamin B12 deficiency and subacute combined degeneration: a case report and literature review.

Introduction: The association between neurological symptomatology and heavy metal exposure has been reported in the literature. A few cases of extrapyramidal symptomatology and subacute combined degeneration have been described as manifestations of mercury intoxication. We highlight a case of a patient presenting with Parkinsonian features (tremor, rigidity, and bradykinesia), pyramidal deficits, dysarthria, paresthesia, mild cognitive decline, and emotional lability, with proven elevated mercury levels in blood and hair and elevated arsenic in urine.

Case: A 60-year-old man, with history of mercury exposure while working at the Centre for Waste Management and Environmental Protection presented to a neurologist after 10 months of persistent tremors, muscle spasms, paresthesia, and irritability, followed by the onset of bradykinesia, slurred speech, rigidity, insomnia, and subtle cognitive decline. Laboratory investigations revealed functional vitamin B12 and vitamin D deficiencies, while toxicological quantitative analysis showed elevated blood mercury levels (15.2 μg/L) and hair root levels (3 μg/g). MRI of the brain was normal, whereas MRI of the posterior cervical spine detected signs of myelopathy. Florodeoxyglucose (FDG) Positron Emission Tomography (PET) of the brain revealed bilateral temporal and parietal glucose hypometabolism, most pronounced in the left inferior parietal and left superior temporal regions. Single-Photon Emission Computed Tomography (SPECT) imaging of dopaminergic neurons in the striatum was negative, and the patient was unresponsive to levodopa. Multivitamin therapy (vitamins B, E, and D) with selenium, in combination with symptomatic therapy (benzodiazepines, muscle relaxants, and antidepressants) provided minimal relief, leading to the introduction of N-acetyl cysteine, which resulted in moderate improvement of symptoms. Physical and speech therapy were of great importance in this case.

Discussion: This case is unique because it represents the development of therapy-resistant extrapyramidal symptoms over 3 years of mercury exposure, likely leading to subacute combined degeneration due to functional vitamin B12 deficiency. Epidemiological data describe methylmercury poisoning, known as Minamata disease, which presents with -somatosensory deficits, ataxia, parkinsonism, dysarthria, and visual and hearing impairments.

Conclusion: Toxicological screening for heavy metals in blood and urine should be considered in patients presenting with unexplained, levodopa-resistant extrapyramidal symptoms, behavioral and sleep disturbances, cognitive decline, and other non-specific neurological signs.

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