1型肌强直性营养不良和肺栓塞:达比加群舒张治疗成功解决血栓。

Q3 Medicine Acta Myologica Pub Date : 2018-09-01
Emanuele Gallinoro, Andrea Antonio Papa, Anna Rago, Simona Sperlongano, Antonio Cassese, Nadia Della Cioppa, Maria Cristina Giada Magliocca, Giovanni Cimmino, Paolo Golino
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引用次数: 0

摘要

1型肌强直性营养不良(DM1)是成人肌肉营养不良最常见的形式。它是一种常染色体显性遗传病,累及多系统。呼吸功能经常受到影响,呼吸衰竭是最常见的死亡原因。肺栓塞是DM1患者呼吸衰竭的罕见原因,因此这些患者的最佳抗凝策略仍不清楚。我们描述的病例肺栓塞在DM1患者,其中肺血栓完全解决与口服达比加群酯治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Myotonic dystrophy type 1 and pulmonary embolism: successful thrombus resolution with dabigatran etexilate therapy.

Myotonic dystrophy type 1 (DM1) is the most common form of adult muscular dystrophy. It is an autosomal dominant inherited disease with multisystemic involvement. Respiratory function is often affected and respiratory failure is the most common cause of death. Pulmonary embolism is a rare cause of respiratory failure in DM1 patients, so that the best anticoagulation strategy in these patients is still unclear. We describe the case of pulmonary embolism in a DM1 patient, in which pulmonary thrombus was completely resolved with oral dabigatran etexilate therapy.

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来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
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0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
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