Background and Purpose-Ischemic symptoms in patients with moyamoya syndrome (MMS) are usually due to hemodynamical ly mediated perfusion failure. and identification of abnormal tissue perfusion in these patients is therefore clinically important. Although dynamic susceptibility contrast (DSC) MRI can be used to study tissue perfusion. there are potential technical problems in MMS. This study investigates the scope and limitations of perfusion MRI in the clinical evaluation of such patients. Methods-Thirteen patients with bilateral MMS were studied with the use of structural. diffusion, and perfusion MRI. The DSC MRI data were analyzed both visually and by a quantitative regional analysis, and the relationship between perfusion Status and clinical symptoms was investigated. Results-Extensive bilateral DSC MRI abnormalities were observed in all the patients. There was a very heterogeneous distribution of bolus arrival time. The areas of abnormality included the major arterial border zones in all cases, although these usually appeared normal on structural and diffusion MRI. Only the most clinically unstable patients had peak width (defined as time to peak minus bolus arrival time) > 5 seconds on the quantitative regional analysis. Several technical limitations of perfusion quantification in MMS are described. as well Lis the implications of these limitations in patients with other forms of occlusive large-vessel disease. Conclusions-The technical limitations of DSC MRI described in this study are important for the accurate interpretation of perfusion MRI in MMS. Despite these limitations, these preliminary findings suggest that the use of quantitative regional analysis of summary parameters may provide clinically useful information in patients with MMS.
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Univ Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Joo, K. D.
Kim, W. S.
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Univ Ulsan, Dept Family Med, Seoul Asan Hosp, Asan Med Ctr,Coll Med, Seoul, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Kim, W. S.
Bae, M. J.
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Univ Ulsan, Dept Family Med, Seoul Asan Hosp, Asan Med Ctr,Coll Med, Seoul, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Bae, M. J.
Choi, M. H.
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Univ Ulsan, Dept Family Med, Seoul Asan Hosp, Asan Med Ctr,Coll Med, Seoul, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Choi, M. H.
Han, J. S.
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Univ Ulsan, Dept Family Med, Seoul Asan Hosp, Asan Med Ctr,Coll Med, Seoul, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Han, J. S.
Jung, J. M.
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Univ Ulsan, Gangneung Asan Hosp, Dept Family Med, Coll Med, Kangnung, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Jung, J. M.
Yang, H. J.
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Univ Ulsan, Gangneung Asan Hosp, Dept Family Med, Coll Med, Kangnung, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea
Yang, H. J.
Lee, J. H.
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Univ Ulsan, Gangneung Asan Hosp, Dept Diagnost Radiol, Coll Med, Kangnung, South KoreaUniv Ulsan, Coll Med, Gangneung Asan Hosp, Dept Neurol, Kangnung, South Korea