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Newly diagnosed PRES in a sickle cell diseased patient: a case report

Sickle cell disease has many clinical impacts, one such rare finding is systemic hypertension although the literature to support it is debatable. Hypertension along with other key components of sickle cell pathology is one of the reversible causes of posterior reversible encephalopathy syndrome (PRE...

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Autores principales: Gurumurthy, Vaishnavi, Jain, Gauri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205325/
https://www.ncbi.nlm.nih.gov/pubmed/37229077
http://dx.doi.org/10.1097/MS9.0000000000000523
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author Gurumurthy, Vaishnavi
Jain, Gauri
author_facet Gurumurthy, Vaishnavi
Jain, Gauri
author_sort Gurumurthy, Vaishnavi
collection PubMed
description Sickle cell disease has many clinical impacts, one such rare finding is systemic hypertension although the literature to support it is debatable. Hypertension along with other key components of sickle cell pathology is one of the reversible causes of posterior reversible encephalopathy syndrome (PRES). Although its triggering factors and pathophysiology is not well documented, hypertension is one of the easily reversible causes of PRES. A well-controlled blood pressure is an aim for reversibility and future recurrence of PRES. However, the addition of other medications like anticonvulsants (levetiracetam and lacosamide) to prevent seizures as a consequence of PRES still remains debatable. Considering the case reported below, the addition of Hydroxyurea to the treatment can be another cause of the recurrence of PRES and needs to be weighed for its risks and benefits.
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spelling pubmed-102053252023-05-24 Newly diagnosed PRES in a sickle cell diseased patient: a case report Gurumurthy, Vaishnavi Jain, Gauri Ann Med Surg (Lond) Case Reports Sickle cell disease has many clinical impacts, one such rare finding is systemic hypertension although the literature to support it is debatable. Hypertension along with other key components of sickle cell pathology is one of the reversible causes of posterior reversible encephalopathy syndrome (PRES). Although its triggering factors and pathophysiology is not well documented, hypertension is one of the easily reversible causes of PRES. A well-controlled blood pressure is an aim for reversibility and future recurrence of PRES. However, the addition of other medications like anticonvulsants (levetiracetam and lacosamide) to prevent seizures as a consequence of PRES still remains debatable. Considering the case reported below, the addition of Hydroxyurea to the treatment can be another cause of the recurrence of PRES and needs to be weighed for its risks and benefits. Lippincott Williams & Wilkins 2023-04-10 /pmc/articles/PMC10205325/ /pubmed/37229077 http://dx.doi.org/10.1097/MS9.0000000000000523 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/) (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Case Reports
Gurumurthy, Vaishnavi
Jain, Gauri
Newly diagnosed PRES in a sickle cell diseased patient: a case report
title Newly diagnosed PRES in a sickle cell diseased patient: a case report
title_full Newly diagnosed PRES in a sickle cell diseased patient: a case report
title_fullStr Newly diagnosed PRES in a sickle cell diseased patient: a case report
title_full_unstemmed Newly diagnosed PRES in a sickle cell diseased patient: a case report
title_short Newly diagnosed PRES in a sickle cell diseased patient: a case report
title_sort newly diagnosed pres in a sickle cell diseased patient: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205325/
https://www.ncbi.nlm.nih.gov/pubmed/37229077
http://dx.doi.org/10.1097/MS9.0000000000000523
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