BackgroundBackground: 123 I-Metaiodobenzylguanidine ( 123 I-MIBG) myocardial scintigraphy is a useful technique to differentiate Parkinson's disease (PD) from atypical parkinsonisms, since it is generally abnormal in PD and normal in the latter. Reduction of myocardial MIBG uptake is a supportive feature in the latest PD diagnostic criteria. Objectives Objectives: To explore the clinical contribution of myocardial scintigraphy in discriminating different forms of parkinsonisms, especially when atypical features are present. Methods Methods: Forty-one patients with parkinsonism underwent a 123 I-MIBG myocardial scintigraphy in our Movement Disorders Center. Disease evolution was reviewed by applying the latest disease criteria for PD, multiple system atrophy (MSA), progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS), as appropriate. Three diagnostic times were defined: T1 (before scintigraphy execution), T2 (immediately after the exam) and T3 (two years later). Early and delayed heart/mediastinum (H/M) ratios and washout rate (WR) were analyzed. Results Results: Myocardial scintigraphy showed impaired MIBG uptake in 12 out of 15 patients with a definite PD diagnosis, while normal uptake was found in 20 of 26 patients with no-PD. Early and delayed H/M ratios were significantly lower in PD compared to overall no-PD patients and MSA patients. 123 I-MIBG myocardial scintigraphy was abnormal in all PD patients with dysautonomia. After 123 I-MIBG myocardial scintigraphy (T2), in 9 patients (22%) an improvement of diagnostic accuracy was reached. Conclusions Conclusions: Diagnostic accuracy of myocardial scintigraphy in distinguishing PD from atypical parkinsonism was suboptimal. Nevertheless, this study confirmed the relevance of 123 I-MIBG myocardial scintigraphy for the discrimination of PD from atypical parkinsonism, especially when dysautonomic symptoms are present.Parkinson's disease (PD) is a chronic progressive neurodegenerative disorder clinically characterized by bradykinesia, rigidity, tremor at rest, and postural abnormalities with gait impairment. 1 Atypical parkinsonisms belong to a group of rare degenerative disorders, presenting with a relatively rapidly progressive parkinsonian syndrome, poor response to dopaminergic treatment, and additional clinical signs. Specifically, Multiple system atrophy (MSA) is characterized by a combination of autonomic failure, parkinsonism, and cerebellar signs. Cardinal features of progressive supranuclear palsy (PSP) include postural instability, early falls, and vertical gaze palsy. Finally, corticobasal syndrome (CBS) presents with an asymmetrical parkinsonism typically associated with limb dystonia, myoclonus, apraxia and alien limb phenomena. 2 Despite their distinct clinical features, the differential diagnosis between PD and atypical parkinsonisms is a recurrent clinical challenge, even among skilled neurologists and