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Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report

Polycythemia vera is a myeloproliferative disorder caused by clonal expansion of erythroid precursors in the bone marrow commonly due to a mutation in the Janus kinase 2 (JAK2) gene located in the short arm of chromosome 9. Hyperviscosity of blood due to high hematocrit causes a low flow state that...

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Autor principal: Krishnan, Prasad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167854/
https://www.ncbi.nlm.nih.gov/pubmed/37181843
http://dx.doi.org/10.4103/bc.bc_37_22
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author Krishnan, Prasad
author_facet Krishnan, Prasad
author_sort Krishnan, Prasad
collection PubMed
description Polycythemia vera is a myeloproliferative disorder caused by clonal expansion of erythroid precursors in the bone marrow commonly due to a mutation in the Janus kinase 2 (JAK2) gene located in the short arm of chromosome 9. Hyperviscosity of blood due to high hematocrit causes a low flow state that may predispose to infarct. These commonly occur in the supratentorial compartment. The case of a 46-year-old man who had an isolated cerebellar infarct with high hematocrit and hemoglobin levels and low serum erythropoietin levels is described. Further investigations eventually led to the unmasking of a JAK2 mutation-negative polycythemia vera.
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spelling pubmed-101678542023-05-10 Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report Krishnan, Prasad Brain Circ Case Report Polycythemia vera is a myeloproliferative disorder caused by clonal expansion of erythroid precursors in the bone marrow commonly due to a mutation in the Janus kinase 2 (JAK2) gene located in the short arm of chromosome 9. Hyperviscosity of blood due to high hematocrit causes a low flow state that may predispose to infarct. These commonly occur in the supratentorial compartment. The case of a 46-year-old man who had an isolated cerebellar infarct with high hematocrit and hemoglobin levels and low serum erythropoietin levels is described. Further investigations eventually led to the unmasking of a JAK2 mutation-negative polycythemia vera. Wolters Kluwer - Medknow 2022-12-06 /pmc/articles/PMC10167854/ /pubmed/37181843 http://dx.doi.org/10.4103/bc.bc_37_22 Text en Copyright: © 2022 Brain Circulation https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Krishnan, Prasad
Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report
title Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report
title_full Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report
title_fullStr Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report
title_full_unstemmed Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report
title_short Isolated cerebellar infarction in a case of JAK 2 mutation-negative polycythemia vera: A case report
title_sort isolated cerebellar infarction in a case of jak 2 mutation-negative polycythemia vera: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167854/
https://www.ncbi.nlm.nih.gov/pubmed/37181843
http://dx.doi.org/10.4103/bc.bc_37_22
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