Assessment of Diffusion and Perfusion Deficits in Patients with Small Subcortical Ischemia

• Published in: American journal of neuroradiology : AJNR Vol. 24; no. 7; pp. 1355 - 1363
• Main Authors: Doege, Claudia A, Kerskens, Christian M, Romero, Berenice I, Brunecker, Peter, Junge-Hulsing, Jan, von Pannwitz, Wolfram, Muller, Bianca, Villringer, Arno
• Format: Journal Article
• Language: English
• Published: United States Am Soc Neuroradiology 01.08.2003; American Society of Neuroradiology
• Subjects: Adult; Aged; Brain; Brain Ischemia - diagnosis; Brain Ischemia - pathology; Brain Ischemia - physiopathology; Cerebral Infarction - diagnosis; Cerebral Infarction - pathology; Cerebral Infarction - physiopathology; Cerebrovascular Circulation - physiology; Diffusion Magnetic Resonance Imaging; Female; Germany; Humans; Magnetic Resonance Angiography; Male; Middle Aged; Prospective Studies; Germany
• ISSN: 0195-6108; 1936-959X

Using perfusion- and diffusion-weighted MR imaging in acute ischemic stroke of the middle cerebral artery (MCA), previous studies have shown a typical pathophysiologic pattern that is characterized by a perfusion deficit larger than the diffusion lesion (mismatch), with the final lesion usually comprising the initial diffusion lesion (core) plus parts of the initial mismatch area. Little is known about underlying pathophysiology in small ischemic stroke. In this study, we used perfusion- and diffusion-weighted MR imaging to investigate the underlying pathophysiology of small subcortical ischemia. Six consecutive patients (age range, 42-76 years) with small subcortical ischemia were examined by using a 1.5-T MR system 2-5, 22-55, and 144-392 hours after the onset of symptoms. T2-weighted, diffusion-weighted imaging at b=0 s/mm2 and b=1000 s/mm2, and bolus-track perfusion-weighted imaging were performed. Lesion sizes were determined on the basis of T2-weighted findings as well as those of apparent diffusion coefficient (ADC) maps and CBF. In every patient, the initial CBF lesion was smaller than the initial ADC lesion. Both the CBF lesion and the ADC lesion increased in size from first to second examination. In all instances, however, the CBF lesion remained smaller than the ADC lesion. The CBF lesion observed during the acute phase and the one seen on the following days were both smaller than the final T2 lesion. Our data suggest that in contrast to previous findings in MCA ischemia in small subcortical infarcts tissue damage may spread beyond the area of the initial perfusion disturbance. In light of the small number of patients, further studies will have to address the relevance of this observation.