HomeStrokeVol. 39, No. 2Global Hemispheric CT Hypoperfusion May Differentiate Headache With Associated Neurological Deficits and Lymphocytosis From Acute Stroke Free AccessReview ArticlePDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessReview ArticlePDF/EPUBGlobal Hemispheric CT Hypoperfusion May Differentiate Headache With Associated Neurological Deficits and Lymphocytosis From Acute Stroke Jacqueline A. Pettersen, MD, MSc, FRCPC, Richard I. Aviv, MBChB, FRCR(UK), Sandra E. Black, MD, FRCPC, Allan J. Fox, MD, FRCPC, Andrew Lim, MD and Brian J. Murray, MD, FRCPC Jacqueline A. PettersenJacqueline A. Pettersen From the LC Campbell Cognitive Neurology Research Unit and Heart and Stroke Foundation Centre for Stroke Recovery (J.A.P., S.E.B.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; the Neuroscience Research Program (J.A.P., R.I.A., S.E.B., A.J.F., B.J.M.), Sunnybrook Research Institute, Toronto, Ontario, Canada; and the Division of Neurology, Department of Medicine (J.A.P., S.E.B., A.L., B.J.M.) and Department of Medical Imaging (R.I.A., A.J.F.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. Search for more papers by this author , Richard I. AvivRichard I. Aviv From the LC Campbell Cognitive Neurology Research Unit and Heart and Stroke Foundation Centre for Stroke Recovery (J.A.P., S.E.B.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; the Neuroscience Research Program (J.A.P., R.I.A., S.E.B., A.J.F., B.J.M.), Sunnybrook Research Institute, Toronto, Ontario, Canada; and the Division of Neurology, Department of Medicine (J.A.P., S.E.B., A.L., B.J.M.) and Department of Medical Imaging (R.I.A., A.J.F.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. Search for more papers by this author , Sandra E. BlackSandra E. Black From the LC Campbell Cognitive Neurology Research Unit and Heart and Stroke Foundation Centre for Stroke Recovery (J.A.P., S.E.B.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; the Neuroscience Research Program (J.A.P., R.I.A., S.E.B., A.J.F., B.J.M.), Sunnybrook Research Institute, Toronto, Ontario, Canada; and the Division of Neurology, Department of Medicine (J.A.P., S.E.B., A.L., B.J.M.) and Department of Medical Imaging (R.I.A., A.J.F.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. Search for more papers by this author , Allan J. FoxAllan J. Fox From the LC Campbell Cognitive Neurology Research Unit and Heart and Stroke Foundation Centre for Stroke Recovery (J.A.P., S.E.B.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; the Neuroscience Research Program (J.A.P., R.I.A., S.E.B., A.J.F., B.J.M.), Sunnybrook Research Institute, Toronto, Ontario, Canada; and the Division of Neurology, Department of Medicine (J.A.P., S.E.B., A.L., B.J.M.) and Department of Medical Imaging (R.I.A., A.J.F.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. Search for more papers by this author , Andrew LimAndrew Lim From the LC Campbell Cognitive Neurology Research Unit and Heart and Stroke Foundation Centre for Stroke Recovery (J.A.P., S.E.B.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; the Neuroscience Research Program (J.A.P., R.I.A., S.E.B., A.J.F., B.J.M.), Sunnybrook Research Institute, Toronto, Ontario, Canada; and the Division of Neurology, Department of Medicine (J.A.P., S.E.B., A.L., B.J.M.) and Department of Medical Imaging (R.I.A., A.J.F.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. Search for more papers by this author and Brian J. MurrayBrian J. Murray From the LC Campbell Cognitive Neurology Research Unit and Heart and Stroke Foundation Centre for Stroke Recovery (J.A.P., S.E.B.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; the Neuroscience Research Program (J.A.P., R.I.A., S.E.B., A.J.F., B.J.M.), Sunnybrook Research Institute, Toronto, Ontario, Canada; and the Division of Neurology, Department of Medicine (J.A.P., S.E.B., A.L., B.J.M.) and Department of Medical Imaging (R.I.A., A.J.F.), Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. Search for more papers by this author Originally published3 Jan 2008https://doi.org/10.1161/STROKEAHA.107.493791Stroke. 2008;39:492–493Other version(s) of this articleYou are viewing the most recent version of this article. Previous versions: January 3, 2008: Previous Version 1 Headache with associated neurological deficits and lymphocytosis (HaNDL) is characterized by temporary recurrent neurological deficits, moderate–severe headache, cerebrospinal fluid lymphocytosis, elevated protein, and increased opening pressure.1 Although CT and MRI should be normal, single photon emission CT may indicate focal hypoperfusion and electroencephalogram may reveal slowing or even epileptiform activity2 resolving once the patient is symptom-free (3 months). Catheter angiography also yields normal results but may trigger an acute neurological episode.3,4Because HaNDL is a benign, self-limited syndrome, it is important to differentiate it from cerebrovascular disease to avoid unnecessary interventions such as catheter angiography and thrombolysis. We present a case initially thought to be acute stroke in which the patient was considered for thrombolysis. CT perfusion changes atypical for stroke made stroke diagnosis questionable and thrombolysis was withheld.Case ReportA 31-year-old man with hypertension, dyslipidemia, and sleep apnea (treated with continuous positive airway pressure), but no history of prior migraine, was brought into our emergency department by ambulance with suspected acute ischemic stroke. He had become aphasic at work so his coworkers called 911. On examination, he was globally aphasic without focal weakness or obvious sensory changes aside from questionable mild right facial paresis (National Institutes of Health Stroke Scale score 6). A noncontrast CT and CT angiogram (CTA) were normal, but CT perfusion revealed a striking pattern of decreased and delayed perfusion to the entire left hemisphere (Figure A). Compared with the right hemisphere, there was a reduction in cerebral blood flow and volume to 80% and 95%, respectively, and the mean transit time was prolonged to 136%, all consistent with a pattern of benign oligemia rather than ischemia.5 Given these findings, he was not offered thrombolysis. Over the subsequent hour, his aphasia began to improve and he reported an evolving severe headache that was alleviated by acetaminophen. By 8 hours postonset, his symptoms had resolved. He experienced a second episode of global aphasia the next day accompanied by right arm paresthesias, which was followed by a severe, albeit gradual-onset, bilateral throbbing headache lasting for several hours. A third episode occurred while the patient was on a day pass 2 days later. He developed a recurrent severe headache with associated nausea/vomiting and concomitant confusion (he ran away from the ambulance attendants) that resolved within 12 hours while back in the hospital. Download figureDownload PowerPointFigure. Axial images reveal (A) prolonged CT mean transit time to the entire left hemisphere relative to the right at presentation (red denotes prolongation); (B) normal MRI fluid-attenuated inversion recovery performed 3 days after the acute event; and (C) normal and symmetric CT mean transit time 6 months postonset.Routine blood work, toxicology, and MRI, including diffusion-weighted imaging, MR angiography, and fluid-attenuated inversion recovery (Figure B), were normal. A lumbar puncture revealed elevated opening pressure of 270 mm H20, increased protein (834 mg/L), and pleocytosis (447×106/mL) with 96% lymphocytes. Glucose and Gram’s stain/culture were normal as was a complete viral workup, including herpes simplex, West Nile, cytomegalovirus, syphilis, and HIV. An electroencephalogram revealed intermittent delta wave slowing and transient sharp waves in the left temporal lobe.The patient was discharged on carbamazepine as a precaution for possible seizures. He had no further neurological episodes or headaches and returned to work. Repeat clinical examination, CT perfusion (see Figure C), electroencephalogram, and formal detailed neuropsychological testing all performed 4 to 7 months later were within normal limits. The carbamazepine was tapered and he remains symptom-free. A final diagnosis of HaNDL was given because his presentation met the diagnostic criteria in the absence of a more likely diagnosis.DiscussionIt is important for neurologists to be aware of HaNDL syndrome. The presentation of sudden-onset neurological deficits illustrates the clinical similarities between HaNDL and acute stroke. A plain CT may be unremarkable in both conditions. However, CT perfusion in acute stroke should reveal significant reductions in cerebral blood flow and possibly cerebral blood volume with a prolongation of mean transit time in an arterial territory. Ischemia of 3 vascular territories is unusual, but theoretically may be produced where an occluded proximal internal carotid artery supplies a fetal-type posterior communicating artery in the absence of an anterior communicating artery. Such an arrangement was excluded by CT angiography as was any vascular occlusion. Furthermore, hemiparesis would be expected with this distribution of ischemia. We speculate that our patient did not experience hemiparesis with such a large affected distribution because the degree of perfusion impairment (ie, oligemia rather than ischemia) may not have reached a unique threshold sufficient to impair motor function. Furthermore, cortical spreading depression may affect a more focal area of the brain reflected by the temporal lobe changes seen on electroencephalogram despite a larger distribution of oligemia that was observed on perfusion imaging. This may explain why language, and not motor function, was impaired in this case.Our findings corroborate those of Fuentes and colleagues2 who demonstrated globally reduced left hemispheric uptake on single photon emission CT during acute aphasia in a HaNDL case. Other reports describing more focal single photon emission CT changes after the acute event3 may have captured resolving perfusion deficits. Transcranial Doppler performed postevent in HaNDL has revealed decreased flow velocities in the ipsilateral middle cerebral artery.6 Taken together, the changes in blood flow and associated electroencephalogram activity further supports the hypothesis that a HaNDL neurological attack may represent a cortical spreading wave of depression with associated oligemia,2 presumed to be due to a viral or postviral etiology.3 Interestingly, perfusion is similarly decreased in migraine aura, although only within the occipital lobe.7To our knowledge, this is the first report of global hemispheric CT perfusion changes during an acute neurological attack of HaNDL. Given the benign, self-limited nature of this syndrome, such a finding in the absence of vascular occlusion may differentiate it from acute stroke avoiding unnecessary interventions. Compared with single photon emission CT, CT perfusion is a more accessible, available, and rapid form of blood flow assessment with less radiation exposure.8 We chose CT perfusion for the investigation of this case because it is routinely used at our center for the evaluation of suspected acute stroke due to its rapid acquisition and processing characteristics. However, it is likely that MR perfusion would have yielded similar hemispheric hypoperfusion findings. We conclude that CT perfusion may help differentiate stroke from the more benign HaNDL syndrome in the acute setting.We thank the patient for agreeing to share details of his clinical assessment. He provided signed informed consent.Sources of FundingJ.A.P. received fellowship funding through the Canadian Institute of Health Research (CIHR) and the Alberta Heritage Foundation of Medical Research (AHFMR).DisclosuresNone.FootnotesCorrespondence to Jacqueline A. Pettersen, MD, MSc, FRCPC, Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, A421-2075 Bayview Avenue, Toronto, Ontario, Canada M4N 3M5. E-mail [email protected] References 1 Headache Classification Subcommittee of the International Headache Society. The international classification of headache disorders: 2nd edition. Cephalalgia. 2004; 24 (suppl 1): 9–160.CrossrefMedlineGoogle Scholar2 Fuentes B, Diez Tejedor E, Pascual J, Coya J, Quirce R. Cerebral blood flow changes in pseudomigraine with pleocytosis analyzed by single photon emission computed tomography. A spreading depression mechanism? Cephalalgia. 1998; 18: 570–573;discussion 531.CrossrefMedlineGoogle Scholar3 Gomez-Aranda F, Canadillas F, Marti-Masso JF, Diez-Tejedor E, Serrano PJ, Leira R, Gracia M, Pascual J. Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis. A report of 50 cases. Brain. 1997; 120: 1105–1113.CrossrefMedlineGoogle Scholar4 Toth CC. Persistent cerebrospinal fluid abnormalities in the syndrome of headache, neurological deficit, and cerebrospinal fluid lymphocytosis despite resolution of clinical symptomatology. Headache. 2002; 42: 1038–1043.CrossrefMedlineGoogle Scholar5 Schaefer PW, Roccatagliata L, Ledezma C, Hoh B, Schwamm LH, Koroshetz W. First-pass quantitative CT perfusion identifies thresholds for salvageable penumbra in acute stroke patients treated with intra-arterial therapy. Am J Neuroradiol. 2006; 27: 20–25.MedlineGoogle Scholar6 Kappler J, Mohr S, Steinmetz H. Cerebral vasomotor changes in the transient syndrome of headache with neurologic deficits and CSF lymphocytosis (HaNDL). Headache. 1997; 37: 516–518.CrossrefMedlineGoogle Scholar7 Cutrer M, Sorensen GA, Weisskoff RM, Ostergaard L, Sanchez del Rio M, Lee EJ, Rosen BR, Moskovitz MA. Perfusion-weighted imaging defects during spontaneous migrainous aura. 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