后天性冯-维勒布兰德综合征并发多发性红细胞症引起的多发性脑栓塞的治疗方法

IF 0.4 Q4 CLINICAL NEUROLOGY
Masashi Watanabe, Haruki Ohtsubo, Akira Shiraoka, Itaru Kyoraku, Kensho Okamoto
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引用次数: 0

摘要

多发性红细胞增多症(PV)是一种罕见的血液疾病,与血栓形成或获得性冯-维勒布兰德综合征(AvWS)相关,但两者同时存在的情况并不多见。在此,我们报告了一名同时患有缺血性脑卒中(IS)和获得性冯-威廉综合征(AvWS)的 59 岁红细胞增多症男性患者。虽然患者没有血栓形成病史,但两年前曾出现难治性鼻衄。脑磁共振成像和血管造影(MRI 和 MRA)显示左侧颈动脉远端有新的 IS 和壁层血栓。实验室检查显示血红蛋白和血细胞比容水平升高,伴有轻度白细胞和血小板增多,与前列腺增生症相符。此外,尽管 von Willebrand 因子的抗原正常,但血小板聚集和活性受到抑制,这表明存在 AvWS。虽然患者拒绝接受建议的羟基脲治疗,但适当的反复抽血成功解决了 MRA 异常,并防止了 IS 复发。本病例强调,对于伴随 AvWS 出现 IS 的 PV 患者,需要采取谨慎的管理措施以防止 IS 复发和大出血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of multiple cerebral embolisms due to polycythemia vera with acquired von Willebrand syndrome
Polycythemia vera (PV) is a rare blood disorder associated with thrombosis or acquired von Willebrand syndrome (AvWS); however, their coexistence is unusual. Here, we report about a 59‐year‐old man with PV who developed both ischemic stroke (IS) and AvWS. Although the patient had no history of thrombosis, he had refractory epistaxis 2 years prior. Brain magnetic resonance imaging and angiography (MRI and MRA) revealed new IS and mural thrombi at the left distal carotid artery. Laboratory investigations showed elevated hemoglobin and hematocrit levels with mild leukocytosis and thrombocytosis, corresponding to PV. Additionally, suppressed platelet aggregation and activity despite normal antigen of von Willebrand factor indicated AvWS. Appropriate repeated phlebotomies successfully resolved the MRA abnormalities and prevented IS recurrence, although the patient refused the recommended treatment with hydroxyurea. This case highlights the need for careful management to prevent recurrent IS and major bleeding in patients with PV who develop IS accompanying AvWS.
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CiteScore
0.80
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