Delayed emergence of parkinson’s disease after reversible manganese-induced parkinsonism: a case report
Year: 2025
Type: article
Study design: Case Report
Abstract: BACKGROUND: Chronic manganese (Mn) exposure, particularly in occupational settings such as welding, can lead to Mn-induced parkinsonism, a condition typically considered reversible and distinct from idiopathic Parkinson's disease (PD). However, the neurotoxic effects of Mn may contribute to or accelerate dopaminergic degeneration in susceptible individuals. CASE PRESENTATION: We report the case of a 53-year-old male welder who initially presented with symmetrical parkinsonism and characteristic T1 hyperintensities in the globus pallidus in Brain MRI, consistent with Mn-induced parkinsonism. Symptoms and Brain MRI abnormalities fully resolved one year after cessation of Mn exposure. Three years later, the patient developed new, progressive, and asymmetric parkinsonian symptoms, including a unilateral resting tremor and bradykinesia. 18- fluoropropyl-2β-carbomethoxy-3β-4-iodophenyl nortropane positron emission tomography imaging demonstrated a marked reduction in striatal dopamine transporter uptake, and the patient responded well to levodopa, confirming the diagnosis of idiopathic PD. CONCLUSIONS: This case illustrates a rare longitudinal transition from reversible Mn-induced parkinsonism to idiopathic PD, suggesting that prior Mn exposure may act as a precipitating or accelerating factor for PD pathogenesis. Functional neuroimaging is critical for differentiating between these two syndromes. This report underscores the importance of long-term neurological follow-up in patients with occupational Mn exposure and supports the hypothesis that environmental toxins can contribute to neurodegenerative processes.
Source: BMC Neurology
Author: Hae-Won Shin
Institutions: Chung-Ang University Healthcare System, Chung-Ang University
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,090
OpenAlex ID: W4415148769
