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Neuropsychological Symptoms After Anterior Cerebral Artery Ischemic Stroke

Published online by Cambridge University Press:  10 July 2020

Michael Kim
Affiliation:
Department of Neurology and Neuroimaging Center (NIC) of the Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz,Mainz, Germany
Annette Spreer
Affiliation:
Department of Neurology and Neuroimaging Center (NIC) of the Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz,Mainz, Germany
Hannah Cuvenhaus
Affiliation:
Edith-Stein-Fachklinik, Bad Bergzabern, Germany
Frank Birklein
Affiliation:
Department of Neurology and Neuroimaging Center (NIC) of the Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz,Mainz, Germany
Frauke Zipp
Affiliation:
Department of Neurology and Neuroimaging Center (NIC) of the Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz,Mainz, Germany
Bernhard Baier*
Affiliation:
Department of Neurology and Neuroimaging Center (NIC) of the Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz,Mainz, Germany Edith-Stein-Fachklinik, Bad Bergzabern, Germany
*
Correspondence to: Bernhard Baier, Department of Neurology, Edith-Stein Fachklinik, Wiesenstraße 25, 76887Bad Bergzabern, Germany. Email: [email protected]
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Abstract

Type
Letter to the Editor
Copyright
© The Author(s), 2020. Published by Cambridge University Press on behalf of The Canadian Journal of Neurological Sciences Inc.

Clinical deficits after ischemic strokes can reflect neurotopological localization of neuronal function. It was shown – based on stroke lesion analysis – that spatial visual hemineglect (HN) and tilt of subjective visual vertical (SVV) were due to lesions affecting the right superior temporal cortex and the insula.Reference Baier, Suchan, Karnath and Dieterich1 These regions are also part of a distributed cortical vestibular network associated with a disturbed vertical perception and pusher phenomenon (PP). Nevertheless, with respect to lesion location, the anterior cerebral artery (ACA) territory is rarely affected in these patients.Reference Baier, Suchan, Karnath and Dieterich1,Reference Karnath, Suchan and Johannsen2 Therefore, the present case report depicts a unique description of a patient presenting vestibular, spatial, and postural deficits due to lesions in the ACA territory.

We report on a 67-year-old man, with no medical history of neurological disease, who developed a paresis of the left lower extremity. Initial computer tomography (CT) scan with CT angiography showed a pericallosal artery occlusion. Magnetic resonance imaging (MRI) three days after stroke onset depicted the acute ischemia in the vascular territory of the right ACA (Figure 1). Seventeen days after stroke onset, the patient had a severe hemiparesis (leg proximal and distal: 0/5; arm proximal and distal 3–4/5 (MRC scaling), dysarthria, as well as a central facial palsy. The muscle reflexes such as the brachioradialis reflex, the biceps reflex, the patellar reflex, and the Achilles reflex were hyperreflexic on the left side; a positive Babinksi response was obtained on the left side. Sensory testing revealed no abnormalities concerning pain, temperature, touch, or vibratory sensation. Due to the paresis, deficits were seen in the coordination such as in the finger-to-nose testing; a dysmetria could not be detected. The patient was unable to stand and walk because of the severe paresis of the lower extremity; thus, heel-to-shin testing and gait testing could not be conducted.

Figure 1: Horizontal T2-fluid-attenuated inversion recovery (FLAIR)-weighted MRI scan three days after stroke onset showed an extended stroke in the territory of the ACA but no ischemic lesions in middle or posterior cerebral artery territory (slice thickness: 5 mm).

Bells test and calculation of Center of Cancellation (CoC) score (0.428) revealed a severe spatial HN.Reference Baier, Suchan, Karnath and Dieterich1 In addition, a severe contraversive PP (score of 3 on the Scale for Contraversive Pushing (SCP)),Reference Karnath and Broetz3 which was tested in a sitting position, a contralesional tilt of SVVReference Baier, Suchan, Karnath and Dieterich1 with a deviation of 6.3°, and a visual extinctionReference Karnath, Baier and Nägele4 could be measured. SVV was measured by means of a luminous rod presented 1.55 m above the ground. The patient wore special goggles with which he was solely able to see the luminous rod. The patient was instructed to sit upright and to keep his head upright. The vertical head position was water level controlled to achieve highest accuracy. The SVV apparatus was positioned 1.50 m in front of the patient. There were three starting positions for the luminous rod: 20°, 30°, and 40° from vertical, each clockwise, and counterclockwise. The patient’s task was to verbally direct the experimenter to orient the luminous rod until “it is exactly vertical.” Each starting position was performed twice in a random order. The experimenter rotated the rod back and forth following the subject’s instructions until the patient was certain that it was exactly vertical. The individual values of the SVV were averaged over the 12 measurements indicating the angle between the SVV and the objective gravitational vertical in the patient’s roll plane.Reference Baier, Suchan, Karnath and Dieterich1 Anosognosia for hemiparesis or disturbed limb ownership was not obtained.Reference Karnath, Baier and Nägele4 The cognitive parameters of the Montreal Cognitive Assessment (MoCA) showed a score of 20 out of 30 indicating cognitive deficits.Reference Nasreddine, Phillips and Bédirian5 Deficits in the MoCA were seen in particular in the delayed recall – indicating a retrieval deficit – and the clock drawing tests (Figure 2); the latter indicated visuospatial deficits.

Figure 2: Clock drawing of the patient showing visuospatial deficits.

From day 17 to day 68 after stroke onset, the patient resided in an inpatient rehabilitation clinic where he received neuropsychological and physical therapy including optokinetic stimulation and therapy to improve spatial perception.

In a second testing, 68 d after stroke, neglect (CoC score of 0.016),Reference Baier, Suchan, Karnath and Dieterich1 PP (SCP score of 0),Reference Karnath and Broetz3 SVV (2.1°),Reference Baier, Suchan, Karnath and Dieterich1 and cognitive deficits (MoCA score of 28) normalized.Reference Nasreddine, Phillips and Bédirian5

Lesions of ACA ischemic strokes are usually not associated with the abovementioned neuropsychological phenomena.Reference Baier, Suchan, Karnath and Dieterich1,Reference Karnath, Suchan and Johannsen2,Reference Karnath and Rorden6 There is only one case in the literature with PP, HN, and disturbed SVV with a similar lesion.Reference Karnath, Suchan and Johannsen2

Our present case indicates that under certain circumstances and detailed investigations, ACA lesions might indeed provoke vestibular, spatial, and postural deficits. Usually, these signs are highly associated with lesions of the insular cortex.Reference Dieterich and Brandt7 The present and the previous casesReference Karnath, Suchan and Johannsen2 indicate that parts of the brain which belong to the ACA territory might be part of a cortical vestibular network and functionally related to the insular cortex, for example, via the superior longitudinal fasciculus which connects frontal, parietal, and insular regions or the adjacent superior occipitofrontal fascicle.Reference Dieterich and Brandt7,Reference Lunven, Thiebaut de Schotten and Bourlon8 It was shown that lesions of both the superior longitudinal fasciculus as well as the inferior occipitofrontal fascicle are affected in acute stroke patients with HN as well as in patients with tilt of SVV.Reference Baier, Suchan, Karnath and Dieterich1,Reference Karnath, Rorden and Ticini9 Thus, these white matter tracts seem to be involved in the vestibulo-cortical network for the perception of verticality in the roll plane as well as in the visuospatial system.

The patient was informed of the intent to publish his case report and gave his written consent. The examination was approved by the ethics committee of the Landesärztekammer Rheinland-Pfalz (#837.032.17 (10,866)) and was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.

Acknowledgments

The present study was supported by a grant from the Deutsche Forschungsgemeinschaft, DFG (BA 4097-1) to B.B. and F.B.

Disclosures

Dr. Zipp reports grants from DFG, grants from BMBF, during the conduct of the study; grants from DFG, grants from BMBF, grants from PMSA, grants from MPG, grants from Genzyme, personal fees from Merck Serono, personal fees from Roche, personal fees from Sanofi-Aventis, personal fees from Celgene, personal fees from ONO, personal fees from Octapharma, outside the submitted work.

Statement of Authorship

MK: conduction of experiments and writing of the MS. AS: design of experiment and writing and supervision of the MS. HC: conduction of the vestibular and neuropsychological testing. FB: writing of the MS, supervision, and financing. FZ: writing of the MS and supervision. BB: writing of the MS, conduction of testing, and supervision.

Footnotes

*

These authors contributed equally to this work.

References

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Figure 0

Figure 1: Horizontal T2-fluid-attenuated inversion recovery (FLAIR)-weighted MRI scan three days after stroke onset showed an extended stroke in the territory of the ACA but no ischemic lesions in middle or posterior cerebral artery territory (slice thickness: 5 mm).

Figure 1

Figure 2: Clock drawing of the patient showing visuospatial deficits.