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“Y形外观”梗死:由原发性血小板增多症引起。

"Y appearance" infarction: caused by essential thrombocythemia.

作者信息

Xiao Shuyue, Ding Yan, Xu Anding, Chen Menglong

机构信息

Department of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, 510630, China.

Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, 510630, China.

出版信息

Thromb J. 2024 Oct 7;22(1):88. doi: 10.1186/s12959-024-00656-x.

Abstract

Essential thrombocythemia (ET) is a myeloproliferative malignancy caused by the excessive proliferation of megakaryocytes in the bone marrow, resulting in the overproduction of peripheral platelets. ET can lead to thrombotic events, such as ischemic stroke (IS), though it is a rare cause of IS. Bilateral medial medullary infarction (BMMI), also known as "Y appearance" infarction due to its distinctive imaging morphology, is a rare clinical subtype of IS which typically has a poor prognosis and a high mortality rate. Herein, we report the case of a 43-year-old male with a history of ET. The patient's platelet count was poorly controlled, and he did not receive regular treatment. After developing symptoms such as dizziness, dysphagia, choking on water, slurred speech, blurred vision, and bilateral limb numbness. Head magnetic resonance imaging revealed a "Y appearance" infarction in the bilateral medial medulla. After admission, the patient was administered intravenous antiplatelet therapy with tirofiban. However, when he was switched to oral aspirin after three days, he experienced decreased muscle strength and worsening symptoms. Therefore, tirofiban was continued for 14 days. Upon discharge, the patient experienced residual limb numbness. His National Institutes of Health Stroke Scale score was 1, Modified Rankin Scale score was 0, and platelet count had decreased to the normal range. During the 9-month follow-up period after discharge, the patient still had only mild limb numbness. Our report presents a special case of "Y appearance" infarction due to ET. Owing to fluctuations in the patient's condition, he received long-term high-dose tirofiban, which ultimately led to a significant improvement in his symptoms.

摘要

原发性血小板增多症(ET)是一种骨髓增殖性恶性肿瘤,由骨髓中巨核细胞过度增殖引起,导致外周血小板过度生成。ET可导致血栓形成事件,如缺血性中风(IS),尽管它是IS的罕见病因。双侧内侧延髓梗死(BMMI),因其独特的影像学形态也被称为“Y形”梗死,是IS的一种罕见临床亚型,通常预后较差且死亡率高。在此,我们报告一例有ET病史的43岁男性病例。患者的血小板计数控制不佳,且未接受正规治疗。在出现头晕、吞咽困难、饮水呛咳、言语含糊、视力模糊和双侧肢体麻木等症状后。头部磁共振成像显示双侧内侧延髓有“Y形”梗死。入院后,患者接受替罗非班静脉抗血小板治疗。然而,三天后改为口服阿司匹林时,他出现肌力下降且症状加重。因此,继续使用替罗非班14天。出院时,患者仍有肢体麻木残留。他的美国国立卫生研究院卒中量表评分为1分,改良Rankin量表评分为0分,血小板计数已降至正常范围。出院后9个月的随访期间,患者仍仅有轻度肢体麻木。我们的报告呈现了一例因ET导致的“Y形”梗死特殊病例。由于患者病情波动,他接受了长期大剂量替罗非班治疗,最终症状有显著改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2186/11460061/b0192c198474/12959_2024_656_Fig1_HTML.jpg

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