Martins De Oliveira Filho Cilomar, Gavralidis Alexander
Mass General Brigham, Salem Hospital, Salem, MA, USA.
Case Rep Hematol. 2022 Nov 22;2022:4948115. doi: 10.1155/2022/4948115. eCollection 2022.
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.
一名60岁女性因头痛、视力模糊、复视和头晕症状持续六周前来就诊。检查发现其血细胞比容升高、血小板增多、铁蛋白水平高,而促红细胞生成素正常。她被诊断为伴有JAK2 V617F突变的真性红细胞增多症。患者接受了磁共振静脉造影,结果显示左侧乙状窦静脉血栓形成。她开始使用低分子量肝素治疗,计划四周后转为口服抗凝治疗,并在三个月后重复进行影像学检查以评估血栓是否溶解。真性红细胞增多症患者可能发生血栓事件,而JAK2突变会进一步增加这种风险。即便如此,颅内静脉血栓形成并非最常见的事件,对于任何出现新的神经系统症状的骨髓增殖性肿瘤患者,都应将其列入鉴别诊断范围。