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首页> 外文期刊>Internal medicine. >Acute Right Heart Failure and Achalasia-like Syndrome in a Patient with Limited Cutaneous Systemic Sclerosis and Primary Biliary Cirrhosis
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Acute Right Heart Failure and Achalasia-like Syndrome in a Patient with Limited Cutaneous Systemic Sclerosis and Primary Biliary Cirrhosis

机译:局限性皮肤系统性硬化症和原发性胆汁性肝硬化患者的急性右心衰竭和急性失语症候群

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摘要

We report a case of a 63-year-old woman who developed acute right heart failure and an achalasia-like syndrome with limited cutaneous systemic sclerosis (lcSSc) and primary biliary cirrhosis. Intravenous administration of diuretics improved her acute heart failure. Anti-centromere antibodies and anti-mitochondria antibodies were present. A coronary angiogram and a Swan-Ganz catheter revealed no abnormalities. Thallium-201 scan at rest demonstrated mild perfusion defects in both the apex and the anteroseptal and the inferior myocardium. A cine-esophagram revealed an achalasia-like syndrome. Though rare, physicians should be aware that some patients with lcSSc may develop acute right heart failure or achalasia-like syndrome.
机译:我们报告了一例63岁的女性,该女性发展为急性右心衰竭和一种局限性皮肤系统性硬化症(lcSSc)和原发性胆汁性肝硬化的门失弛缓样综合征。利尿剂的静脉给药改善了她的急性心力衰竭。存在抗着丝粒抗体和抗线粒体抗体。冠状动脉造影和Swan-Ganz导管未发现异常。静止状态下的scan 201扫描显示先端和前隔以及下下心肌均有轻度的灌注缺陷。电影食管摄影显示出门失弛缓症样综合征。尽管很少见,但医生应注意某些lcSSc患者可能会发展为急性右心衰竭或类似门失弛缓综合征。

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