Case Notes
History
71 year old male presenting with acute onset slurred or muffled speech, no weakness, was able to understand speech, with no loss of consciousness.Exam
Head MR FLAIR Sequence
Arterial stroke is not a single entity, but rather starts as an ictal event generating symptoms and then evolves. However, the ischemic process may have occurred earlier, but was clinically silent, and only becomes symptomatic following clot lysis with downstream secondary embolization or reperfusion hemorrhage. Likewise, collateralization begins immediately. If sufficient the ischemic event ends up as a TIA; if insufficient it ends up a stroke. However, the depth and duration of this event(s) determines whether there is a temporary neurologic deficit, a completed stroke (adds glutamate cascade with vasogenic edema), or a lesser ischemic injury (no glutamate cascade leaving only cytogenic edema). Thus, acute clinical stroke is actually an unstable dynamic process. The CTA venocapillary pool CT density provides information about depth of the ischemic injury at the time of the exam (i.e. is the venocapillary pool normal, or less than normal, or absent), but does not reflect the stroke-age.
MR FLAIR can provide information about stroke-age and depth and duration of the oligemic insult, but cannot distinguish these two effects. FLAIR becomes positive 2-3 hours after the stroke ictus from cytogenic edema (with minimal conspicuity). If the stroke is completed it becomes more positive (obvious conspicuity after 4-6 hours) with the onset of the proinflammatory response producing vasogenic edema. In essence, the conspicuity of FLAIR can reflect either the time of onset and the amount of ischemic injury. If there is no positive FLAIR the onset is either very early or the ischemic injury is minimal. If minimally positive the onset is either in the hyperacute timeframe or the depth of the stroke is less severe. If clearly positive, the stroke is passed the stroke therapy window and is likely likely to have moderate or greater ischemic injury. FLAIR positivity proceeds over time peaking in the acute phase (3 hours to 3 days). Thus, FLAIR adds useful information about the stroke timeline and/or the stroke depth and duration only during the initial period of stroke stabilization or if there has been a new event with progression of clinical findings. Findings on FLAIR, as used in this discussion, is graded as if on a stroke-age timeline (not positive=very early, somewhat positive=early, clearly positive=outside the treatment window). However, the FLAIR conspicuity could just as well be based on the stroke depth and duration (minimal, moderate, or advanced). Nevertheless, the less obvious the FLAIR the earlier the ischemic event for determining stroke therapy or the lesser the stroke injury (which is always good). It is up to the imager to use FLAIR conspicuity language to best fit the clinical context usually determined by timing of the MR exam relative to the stroke ictus and the interval from the CTA.
Purpose
1. Use FLAIR sequence to confirm recognizable ischemic arterial zone or zones (similar to the DWI scenario).
2. Use FLAIR to estimate the most likely stroke-age and/or depth of the ischemic injury based on the conspicuity of the FLAIR compared to the DWI sequences.
3. Use FLAIR to detect thrombus or prior recanalized thrombus (hyperintensity) in the wall of proximal arteries.
4. Use FLAIR to detect focal mass effect and/or whether there is herniation or impending herniation of brain.
Arterial stroke is not a single entity, but rather starts as an ictal event generating symptoms and then evolves. However, the ischemic process may have occurred earlier, but was clinically silent, and only becomes symptomatic following clot lysis with downstream secondary embolization or reperfusion hemorrhage. Likewise, collateralization begins immediately. If sufficient the ischemic event ends up as a TIA; if insufficient it ends up a stroke. However, the depth and duration of this event(s) determines whether there is a temporary neurologic deficit, a completed stroke (adds glutamate cascade with vasogenic edema), or a lesser ischemic injury (no glutamate cascade leaving only cytogenic edema). Thus, acute clinical stroke is actually an unstable dynamic process. The CTA venocapillary pool CT density provides information about depth of the ischemic injury at the time of the exam (i.e. is the venocapillary pool normal, or less than normal, or absent), but does not reflect the stroke-age.
MR FLAIR can provide information about stroke-age and depth and duration of the oligemic insult, but cannot distinguish these two effects. FLAIR becomes positive 2-3 hours after the stroke ictus from cytogenic edema (with minimal conspicuity). If the stroke is completed it becomes more positive (obvious conspicuity after 4-6 hours) with the onset of the proinflammatory response producing vasogenic edema. In essence, the conspicuity of FLAIR can reflect either the time of onset and the amount of ischemic injury. If there is no positive FLAIR the onset is either very early or the ischemic injury is minimal. If minimally positive the onset is either in the hyperacute timeframe or the depth of the stroke is less severe. If clearly positive, the stroke is passed the stroke therapy window and is likely likely to have moderate or greater ischemic injury. FLAIR positivity proceeds over time peaking in the acute phase (3 hours to 3 days). Thus, FLAIR adds useful information about the stroke timeline and/or the stroke depth and duration only during the initial period of stroke stabilization or if there has been a new event with progression of clinical findings. Findings on FLAIR, as used in this discussion, is graded as if on a stroke-age timeline (not positive=very early, somewhat positive=early, clearly positive=outside the treatment window). However, the FLAIR conspicuity could just as well be based on the stroke depth and duration (minimal, moderate, or advanced). Nevertheless, the less obvious the FLAIR the earlier the ischemic event for determining stroke therapy or the lesser the stroke injury (which is always good). It is up to the imager to use FLAIR conspicuity language to best fit the clinical context usually determined by timing of the MR exam relative to the stroke ictus and the interval from the CTA.
Purpose
1. Use FLAIR sequence to confirm recognizable ischemic arterial zone or zones (similar to the DWI scenario).
2. Use FLAIR to estimate the most likely stroke-age and/or depth of the ischemic injury based on the conspicuity of the FLAIR compared to the DWI sequences.
3. Use FLAIR to detect thrombus or prior recanalized thrombus (hyperintensity) in the wall of proximal arteries.
4. Use FLAIR to detect focal mass effect and/or whether there is herniation or impending herniation of brain.
Prior Study
Final Impression for Stroke Protocol CTA1. Prior occlusion of the posterior M3 trunk off the superior division Lt MCA, which has good pial collateral preventing extension of the stroke to most of the posterior superior division perfusion zone.
2. There is acute thrombus in single artery (artery to the central sulcus). The affected perfusion zone for this artery is much smaller than its’ full (normal) perfusion territory, which indicates there has been substantial retrograde pial collateralization from the A4 (ACA) pial vessels. However, there remains a small pial collateral gap in the mid-insula and the adjacent frontoparietal opercular cortex. In this case, the affected area includes the tongue part of the primary facial motor area, which correlates with the patients presenting symptom of dysarthria.
3. The improved CT density in the venocapillary pool is a good indication that the extent of final stroke-zone will remain quite small.
Findings for Diffusion: DWI/ADC Maps
Both the DWI & ADC maps are positive for a small stroke in mid-insula and adjacent intrasylvian frontoparietal operculum. This matches the expected perfusion zone of the proximal part of the artery to the central sulcus vascular territory. Thus, the distal lateral cortical part of the arteries expected perfusion zone is adequately perfused by retrograde ACA (A4) pial collaterals.