Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-m9kch Total loading time: 0 Render date: 2024-05-04T13:27:35.798Z Has data issue: false hasContentIssue false

12 - Behavioral neurology of stroke

from Section III - Diagnostics and syndromes

Published online by Cambridge University Press:  05 May 2010

Michael Brainin
Affiliation:
Zentrum für Klinische Neurowissenschaften, Donnau-Universität, Krems, Austria
Wolf-Dieter Heiss
Affiliation:
Universität zu Köln
Get access

Summary

Cognitive functions are related to our ability to build an internal representation of the world, the conceptual representation system, based on a large-scale neuronal network. This system is connected with more circumscribed and lateralized operational systems that allow us to translate thoughts into words (spoken, written or gestures), images, numbers or other symbols, to store and retrieve information when necessary and to make decisions or act upon them. Most of these operational abilities are subserved by distributed networks with areas of regional specialization, organized according to their specific processing capacities.

The pattern of cognitive/behavioral impairment observed after ischemic stroke is relatively stereotyped, since it follows the distribution of the vascular territories. However, in the hyperacute stage symptoms are likely to be amplified by additional regions of ischemic penumbra, mass effects and diaschisis (impairment of intact regions that are functionally connected with the damaged area), and, in the chronic stage, functional reorganization and brain plasticity mechanisms make neuroanatomical correlations loose and less predictable.

In hemorrhagic lesions, vasculitis, and cerebral venous thrombosis the pattern of cognitive defects is less stereotyped due to the variability of lesion localization, size and number, or particular pathogenic mechanisms that may cause diffuse impairment.

In this chapter we will present the most common cognitive and neurobehavioral deficits secondary to stroke, according to symptom presentation.

Language disorders

Language disorders, or aphasia, occur following perisylvian lesions (middle cerebral artery territory) of the left hemisphere and have a marked impact on the individual quality of life, autonomy and the ability to return to work or previous activities.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Kreisler, A, Godefroy, O, Delmaire, C, Debachy, B, Leclercq, M, Pruvo, JP, et al. The anatomy of aphasia revisited. Neurology 2000; 4:1117–23.CrossRefGoogle Scholar
Martin, A. The representation of object concepts in the brain. Annu Rev Psychol 2007; 58:25–45.CrossRefGoogle Scholar
Saur, D, Lange, R, Baumgaertner, A, Schraknepper, V, Willmes, K, Rijntjes, M, et al. Dynamics of language reorganization after stroke. Brain 2006; 129:1371–1384.CrossRefGoogle ScholarPubMed
Plaut, D, McClelland, J, Seidenberg, M, Patterson, K. Understanding normal and impaired word reading. Psychol Rev 1996; 103:56–115.CrossRefGoogle ScholarPubMed
Lambon Ralph, MA, Graham, NL. Acquired phonological and deep dyslexia. Neurocase 2000; 6:141–3.CrossRefGoogle Scholar
Philipose, , Gottesman, RF, Newhart, M, Kleinman, JT, Herskovits, EH, Pawlak, MA, et al. Neural regions essential for reading and spelling of words and pseudowords. Ann Neurol 2007; 62:481–92.CrossRefGoogle ScholarPubMed
Azouvi, P, Samuel, C, Louis-Dreyfus, A, Bernati, T, Bartolomeo, P, Beis, JM, et al. French Collaborative Study Group on Assessment of Unilateral Neglect (GEREN/GRECO). Sensitivity of clinical and behavioural tests of spatial neglect after right hemisphere stroke. J Neurol Neurosurg Psychiatry 2002; 73:160–6.CrossRefGoogle ScholarPubMed
Hillis, AE, Newhart, M, Heidler, J, Barker, PB, Herskovits, EH, Degaonkar, M. Anatomy of spatial attention: insights from perfusion imaging and hemispatial neglect in acute stroke. J Neurosci 2005; 25:3161–7.CrossRefGoogle ScholarPubMed
Tulving, E. Organization of memory: Quo vadis? In: Gazzaniga, M, ed. The Cognitive Neurosciences. Cambridge: MIT Press; 1995: 839–47.Google Scholar
Valenstein, E, Bowers, D, Verfaellie, M, Heilman, KM, Day, A, Watson, RT. Retrosplenial amnesia. Brain 1987; 110:1631–46.CrossRefGoogle ScholarPubMed
Victor, M, Angevine, JB, Mancall, EL, Fisher, CM. Memory loss with lesions of hippocampal formation. Report of a case with some remarks on the anatomical basis of memory. Arch Neurol 1961; 5:244–63.CrossRefGoogle Scholar
Graff-Radford, NR, Damasio, H, Yamada, T, Eslinger, PJ, Damasio, AR. Nonhaemorrhagic thalamic infarction. Clinical, neuropsychological and electrophysiological findings in four anatomical groups defined by computerized tomography. Brain 1985; 108:485–516.CrossRefGoogle ScholarPubMed
Hackett, ML, Anderson, CS. Health outcomes 1 year after subarachnoid hemorrhage: An international population-based study. The Australian Cooperative Research on Subarachnoid Hemorrhage Study Group. Neurology 2000; 55:658–62.CrossRefGoogle Scholar
Bendel, P, Koivisto, T, Hänninen, T, Kolehmainen, A, Könönen, M, Hurskainen, H, et al. Subarachnoid hemorrhage is followed by temporomesial volume loss: MRI volumetric study. Neurology 2006; 67:575–82.CrossRefGoogle ScholarPubMed
Gilboa, A, Alain, C, Stuss, DT, Melo, B, Miller, S, Moscovitch, M. Mechanisms of spontaneous confabulations: a strategic retrieval account. Brain 2006; 129:1399–1414.CrossRefGoogle ScholarPubMed
Collette, F, Hogge, M, Salmon, E, Linden, M. Exploration of the neural substrates of executive functioning by functional neuroimaging. Neuroscience 2006; 139:209–21.CrossRefGoogle ScholarPubMed
Nys, GM, Zandvoort, MJ, Kort, PL, Jansen, BP, Haan, EH, Kapeplle, LJ. Cognitive disorders in acute stroke: prevelance and clinical determinants. Cerebrovasc Dis 2007; 23:408–16.CrossRefGoogle Scholar
Zinn, S, Bosworth, HB, Hoenig, HM, Swartzwelder, HS. Executive function deficits in acute stroke. Arch Phys Med Rehabil 2007; 88:173–80.CrossRefGoogle ScholarPubMed
Keiter, KT, Copeland, D, Bernardini, GL, Bates, JE, Peery, S, Claassen, J, et al. Predictors of cognitive dysfunction after subarachnoid hemorrhage. Stroke 2002; 33:200–8.CrossRefGoogle Scholar
James, TW, Culham, J, Humphrey, GK, Milner, AD, Goodale, MA. Ventral occipital lesions impair object recognition but not object-directed grasping: an fMRI study. Brain 2003; 126:2463–75.CrossRefGoogle ScholarPubMed
Bouvier, SE, Engel, SA. Behavioral deficits and cortical damage loci in cerebral achromatopsia. Cereb Cortex 2006; 16:183–91.CrossRefGoogle ScholarPubMed
Gobbini, MI, Haxby, JV. Neural systems for recognition of familiar faces. Neuropsychologia 2007; 45:32–41.CrossRefGoogle ScholarPubMed
Sorger, B, Goebel, R, Schiltz, C, Rossion, B. Understanding the functional neuroanatomy of acquired prosopagnosia. Neuroimage 2007; 35:836–52.CrossRefGoogle ScholarPubMed
Brandt, T, Steinke, W, Thie, A, Pessin, MS, Caplan, LR. Posterior cerebral artery territory infarcts: clinical features, infarct topography, causes and outcome. Multicenter results and a review of the literature. Cerebrovasc Dis 2000; 10:170–82.CrossRefGoogle Scholar
Hénon, H, Lebert, F, Durieu, I, Godefroy, O, Lucas, C, Pasquier, F, Leys, D. Confusional state in stroke: relation to preexisting dementia, patient characteristics, and outcome. Stroke 1999; 30:773–9.CrossRefGoogle Scholar
Caeiro, L, Ferro, JM, Albuquerque, R, Figueira, ML. Delirium in the first days of acute stroke. J Neurol 2004; 251:171–8.CrossRefGoogle ScholarPubMed
Gustafson, Y, Olsson, T, Eriksson, S, Asplund, K, Bucht, G. Acute confusional states (delirium) in stroke patients. Cerebrovasc Dis 1991; 1:257–64.CrossRefGoogle Scholar
Sheng, AZ, Shen, Q, Cordato, D, Zhang, YY, Yin Chan, DK. Delirium within three days of stroke in a cohort of elderly patients. J Am Geriatr Soc 2006; 54:1192–8.CrossRefGoogle Scholar
Caeiro, L, Menger, C, Ferro, JM, Albuquerque, R, Figueira, ML. Delirium in acute subarachnoid haemorrhage. Cerebrovasc Dis 2005; 19:31–38.CrossRefGoogle ScholarPubMed
Ghika-Schmid, F, Melle, G, Guex, P, Bogousslavsky, L. Subjective experience and behaviour in acute stroke: the Lausanne Emotion in Acute Stroke Study. Neurology 1999; 52:22–8.CrossRefGoogle ScholarPubMed
Paradiso, S, Robinson, RG, Arndt, S. Self-reported aggressive behavior in patients with stroke. J Nerv Ment Dis 1996; 184:746–53.CrossRefGoogle ScholarPubMed
Kim, JS, Choi, S, Kwon, SU, Seo, YS. Inability to control anger or aggression after stroke. Neurology 2002; 58:1106–8.CrossRefGoogle ScholarPubMed
Santos, CO, Caeiro, L, Ferro, JM, Albuquerque, R, Luísa Figueira, M. Anger, hostility and aggression in the first days of acute stroke. Eur J Neurol 2006; 13:351–8.CrossRefGoogle ScholarPubMed
Chan, KL, Campayo, A, Moser, DJ, Arndt, S, Robinson, RG. Aggressive behavior in patients with stroke: association with psychopathology and results of antidepressant treatment on aggression. Arch Phys Med Rehabil 2006; 87:793–8.CrossRefGoogle ScholarPubMed
Kumral, E, Oztürk, O. Delusional state following acute stroke. Neurology 2004; 62:110–13.CrossRefGoogle ScholarPubMed
Lampl, Y, Lorberboym, M, Gilad, R, Boaz, M, Sadeh, M. Auditory hallucinations in acute stroke. Behav Neurol 2005; 16:211–16.CrossRefGoogle ScholarPubMed
House, A, Dennis, M, Molyneux, A, Warlow, C, Hawton, K. Emotionalism after stroke. BMJ 1989; 298:991–4.CrossRefGoogle ScholarPubMed
Wilson, SAK. Some problems in neurology. II. Pathological laughing and crying. J Neurol Psychopathol 1923; 4:299–333.Google Scholar
Parvizi, J, Anderson, SW, Martin, CO, Damasio, H, Damasio, AR. Pathological laughter and crying: a link to the cerebellum. Brain 2001; 124:1708–19.CrossRefGoogle ScholarPubMed
Coelho, M, Ferro, JM. Fou rire prodromique. Case report and systematic review of literature. Cerebrovasc Dis 2003; 16:101–4.CrossRefGoogle ScholarPubMed
Burvill, PW, Johnson, GA, Jamrozik, KD, Anderson, CS, Stewart-Wynne, EG, Chakera, TM. Anxiety disorders after stroke: results from the Perth Community Stroke Study. Br J Psychiatry 1995; 166:328–32.CrossRefGoogle ScholarPubMed
Aström, M. Generalized anxiety disorder in stroke patients. A 3-year longitudinal study. Stroke 1996; 27:270–5.CrossRefGoogle ScholarPubMed
Robinson, RG. Poststroke anxiety disorders. Clinical and lesion correlates. In: Robinson, RG, ed. The Clinical Neuropsychiatry of Stroke. Cognitive, Behavioral, and Emotional Disorders Following Vascular Brain Injury, 2nd ed. Cambridge: Cambridge University Press; 2006: 326–33.Google Scholar
Bruggimann, L, Annoni, JM, Staub, F, Steinbüchel, N, Linden, M, Bogousslavsky, J. Chronic posttraumatic stress symptoms after nonsevere stroke. Neurology 2006; 66:513–16.CrossRefGoogle ScholarPubMed
Starkstein, SE, Pearlson, GD, Boston, JD, Robinson, RG. Mania after brain injury. A controlled study of causative factors. Arch Neurol 1987; 44:1069–73.CrossRefGoogle ScholarPubMed
Caeiro, L, Ferro, JM, Santos, CO, Figueira, ML. Depression in acute stroke. J Psychiatry Neurosci 2006; 31:377–83.Google ScholarPubMed
Hackett, ML, Yapa, C, Parag, V, Anderson, CS. Frequency of depression after stroke: a systematic review of observational studies. Stroke 2005; 36:1330–40.CrossRefGoogle ScholarPubMed
Carson, AJ, MacHale, S, Allen, K, Lawrie, SM, Dennis, M, House, A, et al. Depression after stroke and lesion location: a systematic review. Lancet 2000; 356:122–6.CrossRefGoogle ScholarPubMed
Hama, S, Yamashita, H, Shigenobu, M, Watanabe, A, Hiramoto, K, Kurisu, K, et al. Depression or apathy and functional recovery after stroke. Int J Geriatr Psychiatry 2007; 22:1046–51.CrossRefGoogle ScholarPubMed
Brodaty, H, Sachdev, PS, Withall, A, Altendorf, A, Valenzuela, MJ, Lorentz, L. Frequency and clinical, neuropsychological and neuroimaging correlates of apathy following stroke – the Sydney Stroke Study. Psychol Med 2005; 35:1707–16.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×