Acute stroke syndromes with isolated hypoperfusion on MRI: a clinical and MRI study

Background: Acute stroke syndromes with negative diffusion-weighted imaging (DWI) but extensive perfusion deficits are rare and constitute a diagnostic challenge due to different operational definitions of penumbral hypoperfusion in acute stroke patients based on MRI criteria. Methods: MR profiles o...

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Hauptverfasser: Alonso, Angelika (VerfasserIn) , Szabo, Kristina (VerfasserIn) , Wolf, Marc (VerfasserIn) , Ebert, Anne (VerfasserIn) , Griebe, Martin (VerfasserIn) , Hennerici, Michael G. (VerfasserIn) , Gass, Achim (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: January 7, 2016
In: European neurology
Year: 2016, Jahrgang: 75, Heft: 1-2, Pages: 27-32
ISSN:1421-9913
DOI:10.1159/000443305
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1159/000443305
Verlag, Volltext: https://www-karger-com.ezproxy.medma.uni-heidelberg.de/Article/FullText/443305
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Verfasserangaben:Angelika Alonso, Kristina Szabo, Marc E. Wolf, Anne D. Ebert, Martin Griebe, Michael G. Hennerici, Achim Gass

MARC

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520 |a Background: Acute stroke syndromes with negative diffusion-weighted imaging (DWI) but extensive perfusion deficits are rare and constitute a diagnostic challenge due to different operational definitions of penumbral hypoperfusion in acute stroke patients based on MRI criteria. Methods: MR profiles of 19 patients presenting with acute stroke syndromes with negative DWI in the presence of an extensive area of hypoperfusion on time-to-peak (TTP) maps of dynamic susceptibility contrast perfusion-weighted imaging (PWI) were analysed. DWI and PWI lesions were quantified and interpreted with regard to the clinical course. Results: Despite the large area of abnormal perfusion on TTP maps, the clinical course was benign (median National Institute of Health Stroke Scale 2 at admission, 0 at discharge). The volume of hypoperfused tissue was significantly smaller on postprocessed TTP maps with a TTP delay of >4 s than on unprocessed TTP maps with manual contrast adjustment. Semiquantitatively assessed TTP lesion volume was associated with the presence of DWI lesions on follow-up. Conclusion: TTP maps are highly sensitive to demonstrate even small-scale perfusion abnormalities. The additional information from TTP delay thresholds indicates critically reduced perfusion and appears to be a good prognostic indicator in combination with MR angiography and symptomatology. 
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