Successful treatment of acute right cardiac failure due to pulmonary thromboembolism in mixed connective tissue disease.

Y Ueda, Y Yamauchi, K Makizumi, R Kaji, H Ishibashi, K Nagasawa, Y Niho
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引用次数: 6

Abstract

Mixed connective tissue disease (MCTD) is characterized as a benign rheumatic disease with a favorable response to therapy. When pulmonary hypertension is a complication, however, it is often reported to be fatal. A 32-year-old female patient with MCTD who had developed rapidly progressive pulmonary hypertension and disseminated intravascular coagulopathy was admitted to our hospital and was successfully treated with corticosteroids and anticoagulants. The failure of microcirculation due to coagulopathy is considered to be one of the possible entities of pulmonary hypertension.

混合性结缔组织病肺血栓栓塞所致急性右心衰的成功治疗。
混合性结缔组织病(MCTD)是一种对治疗有良好反应的良性风湿病。然而,当肺动脉高压是一种并发症时,它通常是致命的。一名32岁女性MCTD患者因发展为快速进展性肺动脉高压和弥散性血管内凝血功能障碍而入住我院,并成功应用皮质类固醇和抗凝剂治疗。凝血功能障碍引起的微循环衰竭被认为是肺动脉高压的可能病因之一。
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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