[Pulmonary thromboembolism associated with antiphospholipid syndrome in scleroderma].

R. Tazawa, Y. Saijo, T. Abe, K. Satoh, A. Watanabe, S. Yamaki, T. Nukiwa
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引用次数: 2

Abstract

A 51-year-old woman was referred to our hospital with dyspnea. Chest roentgenogram on admission showed dilation of the pulmonary arteries and hyperlucency in the lung fields. An ultrasonic cardiographic examination showed that the right atrium and ventricle were dilated. Pulmonary thromboembolism due to left popliteal vein thrombosis was diagnosed by perfusion scintigram of the lung, which showed multiple wedge-shaped defects, and by digital subtraction angiogram, which showed a filing defect in the left popliteal vein. Antiphospholipid syndrome was diagnosed after IgG anticardiolipin antibody was defected. Scleroderma was subsequently diagnosed because the patient exhibited Raynaud's phenomenon and proximal scleroderma. Although closely associated with lupus erythematosus and other lupus variants, antiphospholipid syndrome has not been recognized as a common complication of scleroderma. This is the first report of a patient with pulmonary thromboembolism associated with antiphospholipid syndrome and scleroderma.
[硬皮病患者肺血栓栓塞与抗磷脂综合征相关]。
一名51岁女性因呼吸困难转诊至我院。入院时的胸片显示肺动脉扩张和肺野高透光。超声心动图检查显示右心房和右心室扩张。肺灌注闪烁图显示多发楔形缺损,数字减影血管造影显示左腘静脉呈锉状缺损,诊断为左腘静脉血栓形成所致肺血栓栓塞。检测抗心磷脂抗体IgG后诊断为抗磷脂综合征。由于患者表现出雷诺现象和近端硬皮病,因此被诊断为硬皮病。虽然与红斑狼疮和其他狼疮变体密切相关,但抗磷脂综合征尚未被认为是硬皮病的常见并发症。这是第一例与抗磷脂综合征和硬皮病相关的肺血栓栓塞患者的报告。
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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