2009
DOI: 10.1179/016164109x12445505689607
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Clinically presenting acute/subacute ischemic stroke: differential diagnosis of the non-enhanced CT hypodensity by advanced neuroimaging

Abstract: As presented in this review, although several diseases initially present a diagnostic dilemma upon presentation because of their clinical and non-enhanced CT similarities to cerebral infarction, advanced diagnostic neuroimaging readily establishes their unique pathologies.

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Cited by 6 publications
(3 citation statements)
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“…However, in the clinical setting, old cerebral infarction (OCI) and asymmetric leukoaraiosis (LA) similarly display slightly hypodense lesions. Thus, it is sometimes challenging to distinguish AIS from these two types of lesions [ 5 ]. AIS and OCI can occur anywhere in the brain and present as solitary or multiple lesions, especially in the basal ganglia region.…”
Section: Introductionmentioning
confidence: 99%
“…However, in the clinical setting, old cerebral infarction (OCI) and asymmetric leukoaraiosis (LA) similarly display slightly hypodense lesions. Thus, it is sometimes challenging to distinguish AIS from these two types of lesions [ 5 ]. AIS and OCI can occur anywhere in the brain and present as solitary or multiple lesions, especially in the basal ganglia region.…”
Section: Introductionmentioning
confidence: 99%
“…However, the treatment of intravenous thrombolysis with recombinant tissue thrombolytic plasminogen activator (rt-PA) window-time is very narrow, usually within 3.0–4.5 h after the onset of neurologic symptoms, which delays the diagnostic time for visible neuroimaging techniques [ 5 , 6 ]. On the other hand, it is difficult to distinguish ischemic stroke subtypes from these similar focal neurological deficits, such as complex migraine, demyelinating diseases, and vascular diseases [ 7 ]. In addition, the utility of advanced MRI technology current is limited because of lacking available emergency services or vascular neurologists [ 8 ].…”
Section: Introductionmentioning
confidence: 99%
“…However, the treatment of intravenous thrombolysis with recombinant tissue thrombolytic plasminogen activator (rt-PA) window-time is very narrow, usually within 3.0-4.5 hours after the onset of neurologic symptoms, which delays the diagnostic time for visible neuroimaging techniques [5,6]. On the other hand, it is di cult to distinguish ischemic stroke subtypes from these similar focal neurological de cits, such as complex migraine, demyelinating diseases, metabolic and vascular diseases [7]. In addition, the utility of advanced MRI technology current is limited because of lacking available emergency services or vascular neurologists [8].…”
Section: Introductionmentioning
confidence: 99%