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首页> 外文期刊>Journal of cardiology >Silent pulmonary artery dissection in a patient with Eisenmenger syndrome due to ventricular septal defect: a case report.
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Silent pulmonary artery dissection in a patient with Eisenmenger syndrome due to ventricular septal defect: a case report.

机译:因室间隔缺损而引起的艾森曼格综合征患者的肺动脉静默解剖:一例报告。

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摘要

A 62-year-old woman was admitted to our hospital because of fever in August 2002. She had been treated under a diagnosis of Eisenmenger syndrome with ventricular septal defect since 1988. On admission, echocardiography and color Doppler echocardiography revealed a markedly enlarged pulmonary artery with a mobile flap, and dissection of the pulmonary artery. The origin of the fever could not be identified, and the fever subsided spontaneously without specific treatment. She had no chest pain, but fever might have been a sign of dissection in this patient. Longstanding pulmonary hypertension may cause dissection, which may lead to sudden death or pulmonary hemorrhage often seen in patients with Eisenmenger syndrome. Our patient was a rare survivor without serious bleeding complication.
机译:一名62岁的妇女因发烧于2002年8月入我院。她于1988年开始接受诊断为艾森曼格综合征并伴有室间隔缺损的治疗。入院时,超声心动图和彩色多普勒超声心动图显示肺动脉明显肿大皮瓣活动,并解剖肺动脉。无法确定发烧的起源,如果没有特殊治疗,发烧会自发消退。她没有胸痛,但发烧可能是该患者解剖的迹象。长期存在的肺动脉高压可能会导致解剖,这可能会导致艾森曼格综合征患者经常发生的猝死或肺出血。我们的患者是罕见的幸存者,没有严重的出血并发症。

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