2004
DOI: 10.1016/j.parkreldis.2004.04.008
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Comparison of magnetic resonance imaging in subtypes of multiple system atrophy

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Cited by 73 publications
(67 citation statements)
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References 30 publications
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“…In the previous study, the FLAIR sequence was performed at a lower 1.0-tesla magnetic field strength, so the difference in the magnetic field strength, which affects the signal-to-noise ratio, was assumed to a reason for the higher sensitivity detected in our study. Contrary to the results of the present study, a previous study reported that FLAIR displayed low specificity for the diagnosis of MSA [26]. The reason for this was not discussed, but mild slit-like hyperintensity of the lateral putamen caused by age-related reactive gliosis might have caused this misinterpretation [6].…”
Section: Discussioncontrasting
confidence: 99%
See 1 more Smart Citation
“…In the previous study, the FLAIR sequence was performed at a lower 1.0-tesla magnetic field strength, so the difference in the magnetic field strength, which affects the signal-to-noise ratio, was assumed to a reason for the higher sensitivity detected in our study. Contrary to the results of the present study, a previous study reported that FLAIR displayed low specificity for the diagnosis of MSA [26]. The reason for this was not discussed, but mild slit-like hyperintensity of the lateral putamen caused by age-related reactive gliosis might have caused this misinterpretation [6].…”
Section: Discussioncontrasting
confidence: 99%
“…In addition, in the present study, the subjects with a symptom duration shorter than 4 years tended not to display HPR on T2W sequences (false negativity rate: 57%, 8/14). Thus, the low sensitivity of T2W sequences for detecting HPR poses a diagnostic problem in spite of its higher specificity compared with other findings such as putaminal hypointensity [26,27]. However, in these studies, the presence of HPR was only evaluated on T2W sequences.…”
Section: Discussionmentioning
confidence: 99%
“…2 ), atrophy of the cerebellum, and hyperintensity in the middle cerebellar peduncle (MCP) [38,43,[51][52][53] . When comparing MSA-P with MSA-C, putaminal abnormalities at 1.5 T seem to appear more often and earlier in MSA-P than MSA-C, and conversely infratentorial abnormalities seem to appear more often and earlier in MSA-C than in MSA-P [54][55][56] . Specificity of abnormalities to differentiate MSA from PD and healthy controls is considered quite high, whereas sensitivity -particularly in early disease stages -seems to be insufficient [38,53,54,57] .…”
Section: Summary Of the Mr-based Neuroimaging Studies In The Differenmentioning
confidence: 82%
“…When comparing MSA-P with MSA-C, putaminal abnormalities at 1.5 T seem to appear more often and earlier in MSA-P than MSA-C, and conversely infratentorial abnormalities seem to appear more often and earlier in MSA-C than in MSA-P [54][55][56] . Specificity of abnormalities to differentiate MSA from PD and healthy controls is considered quite high, whereas sensitivity -particularly in early disease stages -seems to be insufficient [38,53,54,57] . For instance, putaminal atrophy appears to specifically delineate MSA from PD, but T 2 putaminal hypointensity and a putaminal hyperintense rim may be observed in both diseases [55,[58][59][60] .…”
Section: Summary Of the Mr-based Neuroimaging Studies In The Differenmentioning
confidence: 82%
“…Other disorders associated with parkinsonism, such as Parkinson's disease with autonomic failure, progressive supranuclear palsy (PSP), and diffuse Lewy body disease (DLBD), may often be misdiagnosed as MSA-P [7,8,9,10,11,12]. A neuropathological study showed that Table 1.…”
Section: Discussionmentioning
confidence: 99%