2616 Unilateral posterior reversible encephalopathy syndrome: a case of Hickam’s Dictum

ObjectiveTo describe a rare and diagnostically challenging case of unilateral posterior reversible encephalopathy syndrome (PRES), contralateral to a chronically occluded right internal carotid artery (ICA), in a patient with multiple sclerosis (MS).BackgroundPRES is a clinicoradiological diagnosis...

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Veröffentlicht in:BMJ neurology open 2023-08, Vol.5 (Suppl 1), p.A21-A21
Hauptverfasser: Hayes, Michael TG, Lefever, Kristen, Devlin, Michael
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creator Hayes, Michael TG
Lefever, Kristen
Devlin, Michael
description ObjectiveTo describe a rare and diagnostically challenging case of unilateral posterior reversible encephalopathy syndrome (PRES), contralateral to a chronically occluded right internal carotid artery (ICA), in a patient with multiple sclerosis (MS).BackgroundPRES is a clinicoradiological diagnosis based on typical clinical features and risk factors, supported by MRI findings. MRI typically shows bilateral cortical and subcortical vasogenic oedema. Cases involving unilateral vasogenic oedema are very rare.Case PresentationWe report the case of a 66-year-old female brought to the emergency department as a code stroke for right-sided hemiplegia preceded by her first ever seizure. She was confused and severely hypertensive on arrival. CT stroke protocol showed a chronically occluded right ICA, delayed cerebral perfusion in the right anterior circulation and no core infarct. MRI findings were consistent with vasogenic oedema in the superior left frontal and parietal lobes. The patient had multiple sclerosis with preexisting periventricular white matter lesions, one of which had enlarged on her most recent surveillance MRI. She had not been taking disease modifying therapy for the past 10 years. CSF studies for infectious aetiologies were negative. A left renal artery occlusion was identified and treated conservatively. The hypertension resolved with medical therapy. The patient recovered and a follow-up MRI showed resolution of vasogenic oedema.ConclusionThis case illustrates a rare presentation of unilateral PRES. An occluded ICA protected the ipsilateral anterior circulation from the significantly elevated perfusion pressures, and subsequent endothelial dysfunction, experienced by the contralateral hemisphere in the setting of severe hypertension.
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MRI typically shows bilateral cortical and subcortical vasogenic oedema. Cases involving unilateral vasogenic oedema are very rare.Case PresentationWe report the case of a 66-year-old female brought to the emergency department as a code stroke for right-sided hemiplegia preceded by her first ever seizure. She was confused and severely hypertensive on arrival. CT stroke protocol showed a chronically occluded right ICA, delayed cerebral perfusion in the right anterior circulation and no core infarct. MRI findings were consistent with vasogenic oedema in the superior left frontal and parietal lobes. The patient had multiple sclerosis with preexisting periventricular white matter lesions, one of which had enlarged on her most recent surveillance MRI. She had not been taking disease modifying therapy for the past 10 years. CSF studies for infectious aetiologies were negative. A left renal artery occlusion was identified and treated conservatively. The hypertension resolved with medical therapy. The patient recovered and a follow-up MRI showed resolution of vasogenic oedema.ConclusionThis case illustrates a rare presentation of unilateral PRES. An occluded ICA protected the ipsilateral anterior circulation from the significantly elevated perfusion pressures, and subsequent endothelial dysfunction, experienced by the contralateral hemisphere in the setting of severe hypertension.</description><identifier>EISSN: 2632-6140</identifier><identifier>DOI: 10.1136/bmjno-2023-ANZAN.56</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Edema ; Hypertension ; Multiple sclerosis ; Poster Abstract</subject><ispartof>BMJ neurology open, 2023-08, Vol.5 (Suppl 1), p.A21-A21</ispartof><rights>Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2023 Author(s) (or their employer(s)) 2023. No commercial re-use. 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MRI typically shows bilateral cortical and subcortical vasogenic oedema. Cases involving unilateral vasogenic oedema are very rare.Case PresentationWe report the case of a 66-year-old female brought to the emergency department as a code stroke for right-sided hemiplegia preceded by her first ever seizure. She was confused and severely hypertensive on arrival. CT stroke protocol showed a chronically occluded right ICA, delayed cerebral perfusion in the right anterior circulation and no core infarct. MRI findings were consistent with vasogenic oedema in the superior left frontal and parietal lobes. The patient had multiple sclerosis with preexisting periventricular white matter lesions, one of which had enlarged on her most recent surveillance MRI. She had not been taking disease modifying therapy for the past 10 years. CSF studies for infectious aetiologies were negative. A left renal artery occlusion was identified and treated conservatively. The hypertension resolved with medical therapy. The patient recovered and a follow-up MRI showed resolution of vasogenic oedema.ConclusionThis case illustrates a rare presentation of unilateral PRES. An occluded ICA protected the ipsilateral anterior circulation from the significantly elevated perfusion pressures, and subsequent endothelial dysfunction, experienced by the contralateral hemisphere in the setting of severe hypertension.</description><subject>Edema</subject><subject>Hypertension</subject><subject>Multiple sclerosis</subject><subject>Poster Abstract</subject><issn>2632-6140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpFkL1OwzAUhS0kJKrSJ2CxxJzWf7lx2KryU6SqLHSBwbIdR01J4hCnSN268BC8Xp-EtEViOmf4dO_Rh9ANJWNKOUxMtal9xAjj0XT5Nl2OY7hAAwacRUAFuUKjEDaEEBYTIVMxQO8MKBz236u6KHXnWl3ixoe-FL7FrftybShM6bCrrWvWuvSN7tY7HHZ11vrK3WGNrQ4O-xzPC_uhq8P-J-D7wnbb6hpd5roMbvSXQ7R6fHidzaPFy9PzbLqIzHFzRK0kAgwVIIXJAMBoyTVkKWfWxjkTPIt1YnJDQBLJODhjcsZja5wEmeZ8iG7Pd5vWf25d6NTGb9u6f6lYyihNeZLInpqcqd7RP0CJOo5QJ3HqKE6dxKkY-C_yemZT</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Hayes, Michael TG</creator><creator>Lefever, Kristen</creator><creator>Devlin, Michael</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><scope>K9.</scope></search><sort><creationdate>202308</creationdate><title>2616 Unilateral posterior reversible encephalopathy syndrome: a case of Hickam’s Dictum</title><author>Hayes, Michael TG ; Lefever, Kristen ; Devlin, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1136-1c8046b14684bd666ba83a6d932cc5f243d5a7bfb06808236ebbf235cbe8689f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Edema</topic><topic>Hypertension</topic><topic>Multiple sclerosis</topic><topic>Poster Abstract</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hayes, Michael TG</creatorcontrib><creatorcontrib>Lefever, Kristen</creatorcontrib><creatorcontrib>Devlin, Michael</creatorcontrib><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>BMJ neurology open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Hayes, Michael TG</au><au>Lefever, Kristen</au><au>Devlin, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2616 Unilateral posterior reversible encephalopathy syndrome: a case of Hickam’s Dictum</atitle><jtitle>BMJ neurology open</jtitle><stitle>BMJ Neurol Open</stitle><date>2023-08</date><risdate>2023</risdate><volume>5</volume><issue>Suppl 1</issue><spage>A21</spage><epage>A21</epage><pages>A21-A21</pages><eissn>2632-6140</eissn><abstract>ObjectiveTo describe a rare and diagnostically challenging case of unilateral posterior reversible encephalopathy syndrome (PRES), contralateral to a chronically occluded right internal carotid artery (ICA), in a patient with multiple sclerosis (MS).BackgroundPRES is a clinicoradiological diagnosis based on typical clinical features and risk factors, supported by MRI findings. MRI typically shows bilateral cortical and subcortical vasogenic oedema. Cases involving unilateral vasogenic oedema are very rare.Case PresentationWe report the case of a 66-year-old female brought to the emergency department as a code stroke for right-sided hemiplegia preceded by her first ever seizure. She was confused and severely hypertensive on arrival. CT stroke protocol showed a chronically occluded right ICA, delayed cerebral perfusion in the right anterior circulation and no core infarct. MRI findings were consistent with vasogenic oedema in the superior left frontal and parietal lobes. The patient had multiple sclerosis with preexisting periventricular white matter lesions, one of which had enlarged on her most recent surveillance MRI. She had not been taking disease modifying therapy for the past 10 years. CSF studies for infectious aetiologies were negative. A left renal artery occlusion was identified and treated conservatively. The hypertension resolved with medical therapy. The patient recovered and a follow-up MRI showed resolution of vasogenic oedema.ConclusionThis case illustrates a rare presentation of unilateral PRES. An occluded ICA protected the ipsilateral anterior circulation from the significantly elevated perfusion pressures, and subsequent endothelial dysfunction, experienced by the contralateral hemisphere in the setting of severe hypertension.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><doi>10.1136/bmjno-2023-ANZAN.56</doi><oa>free_for_read</oa></addata></record>
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subjects Edema
Hypertension
Multiple sclerosis
Poster Abstract
title 2616 Unilateral posterior reversible encephalopathy syndrome: a case of Hickam’s Dictum
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