Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera

A 60-year-old female presented with headaches, blurry vision, diplopia, and dizziness for six weeks. Her workup revealed an elevated hematocrit, thrombocytosis, high ferritin, and normal erythropoietin. She was diagnosed with polycythemia vera with the JAK2 V617F mutation. The patient underwent magn...

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Main Authors: Cilomar Martins De Oliveira Filho, Alexander Gavralidis
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2022/4948115
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author Cilomar Martins De Oliveira Filho
Alexander Gavralidis
author_facet Cilomar Martins De Oliveira Filho
Alexander Gavralidis
author_sort Cilomar Martins De Oliveira Filho
collection DOAJ
description A 60-year-old female presented with headaches, blurry vision, diplopia, and dizziness for six weeks. Her workup revealed an elevated hematocrit, thrombocytosis, high ferritin, and normal erythropoietin. She was diagnosed with polycythemia vera with the JAK2 V617F mutation. The patient underwent magnetic resonance venography, which showed left-sided sigmoid venous thrombosis. She was placed on low-molecular-weight heparin, with a plan to transition to oral anticoagulation after four weeks and repeat imaging in three months to assess for resolution. Thrombotic events may occur in patients with polycythemia vera, and a JAK2 mutation further heightens that risk. Even so, intracranial venous thrombosis is not among the most common events, and it should be kept in the differential for any patient with myeloproliferative neoplasms presenting with new neurological symptoms.
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spelling doaj-art-fbeb2a6442984d9387560214fa7d54e62025-02-03T01:00:43ZengWileyCase Reports in Hematology2090-65792022-01-01202210.1155/2022/4948115Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia VeraCilomar Martins De Oliveira Filho0Alexander Gavralidis1Mass General BrighamMass General BrighamA 60-year-old female presented with headaches, blurry vision, diplopia, and dizziness for six weeks. Her workup revealed an elevated hematocrit, thrombocytosis, high ferritin, and normal erythropoietin. She was diagnosed with polycythemia vera with the JAK2 V617F mutation. The patient underwent magnetic resonance venography, which showed left-sided sigmoid venous thrombosis. She was placed on low-molecular-weight heparin, with a plan to transition to oral anticoagulation after four weeks and repeat imaging in three months to assess for resolution. Thrombotic events may occur in patients with polycythemia vera, and a JAK2 mutation further heightens that risk. Even so, intracranial venous thrombosis is not among the most common events, and it should be kept in the differential for any patient with myeloproliferative neoplasms presenting with new neurological symptoms.http://dx.doi.org/10.1155/2022/4948115
spellingShingle Cilomar Martins De Oliveira Filho
Alexander Gavralidis
Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera
Case Reports in Hematology
title Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera
title_full Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera
title_fullStr Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera
title_full_unstemmed Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera
title_short Sigmoid Venous Thrombosis in JAK2 V617F Mutated Polycythemia Vera
title_sort sigmoid venous thrombosis in jak2 v617f mutated polycythemia vera
url http://dx.doi.org/10.1155/2022/4948115
work_keys_str_mv AT cilomarmartinsdeoliveirafilho sigmoidvenousthrombosisinjak2v617fmutatedpolycythemiavera
AT alexandergavralidis sigmoidvenousthrombosisinjak2v617fmutatedpolycythemiavera