The clinical distinction of Parkinson's disease (PD) from other disorders w
ith parkinsonian features is often difficult. Routine magnetic resonance im
aging of the brain (MRI) is typically normal in patients with PD. However,
it can be helpful in supporting a diagnosis of atypical parkinsonian disord
ers and excluding non-parkinsonian disorders that can mimic parkinsonism, s
uch as vascular parkinsonism or hydrocephalus. MRI in atypical parkinsonian
syndromes, such as multiple-system atrophy (MSA), progressive supranuclear
palsy (PSP) and corticobasal degeneration (CBD) can reveal characteristic
features that cannot only differentiate these syndromes from PD, but also h
elp to differentiate between these atypical disorders. These features inclu
de a hyperintense rim at the lateral putaminal edge and infratentorial sign
al change and atrophy in MSA, marked atrophy and hyperintensity of the midb
rain on T-2-weighted images in PSP, and asymmetrical parieto-frontal atroph
y in CBD. Although these findings are very specific, they are present in on
ly a proportion of patients with these diseases. MRI-spectroscopy (1H-MRS)
of the lentiform nucleus is similarly normal in patients with PD, but can s
how a reduced ratio of N-acetyl-aspartate (NAA) to creatine-phosphocreatine
(Cre) or choline (Cho) concentration in atypical parkinsonian disorders. T
he pattern of reduction of NAA/Cre or NAA/Cho in other areas of the brain m
ay also help to differentiate between atypical parkinsonian syndromes. Rout
ine-MRI and MRI-spectroscopy are useful tools to improve clinical diagnosis
of parkinsonian syndromes.