一名患有 APML 和 21 三体综合征的儿童的主动脉瓣血栓、中风和血管内血栓切除术。

IF 0.9 4区 医学 Q4 HEMATOLOGY Journal of Pediatric Hematology/Oncology Pub Date : 2024-07-01 Epub Date: 2024-06-05 DOI:10.1097/MPH.0000000000002858
Gayathri Plant, Adam Kirton, Gregory M T Guilcher, Mohammad AlNajjar, Kandice Mah, Alim P Mitha, Jay Riva-Cambrin, MacGregor Steele
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引用次数: 0

摘要

APML 是急性髓性白血病的一种亚型,治愈率高达 90% 以上。尽管治疗效果显著,但 APML 由于之前经常发生弥散性血管内凝血,因此出血风险较高。血栓形成的风险较少被认识到,但却至关重要。我们记录了一个独特的儿科病例:一名 13 岁的 21 三体综合征患儿被诊断为 APML,无症状的主动脉瓣血栓导致血栓栓塞性动脉缺血性中风。通过血管内血栓切除术,重新建立了脑循环,取出了带有 APML 细胞的纤维蛋白血栓。神经功能迅速恢复。该报告强调了警惕 APML 血栓并发症的重要性,突出了被忽视的风险的潜在严重性。
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Aortic Valve Thrombus, Stroke, and Endovascular Thrombectomy in a Child With APML and Trisomy 21.

APML, a subtype of acute myeloid leukemia, is highly curable, with cure rates over 90%. Despite its therapeutic success, APML poses elevated bleeding risks due to frequent prior disseminated intravascular coagulation. Less commonly recognized but critical is the thrombotic risk. We document a unique pediatric case: a 13-year-old with trisomy 21 diagnosed with APML had an asymptomatic aortic valve thrombus leading to thromboembolic arterial ischemic stroke. Through endovascular thrombectomy, cerebral circulation was re-established, extracting a fibrin thrombus with APML cells. Neurological recovery was swift. This report underscores the importance of vigilance for thrombotic complications in APML, highlighting the potential severity of overlooked risks.

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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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