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一名患有三房心的成年男性先天性二尖瓣狭窄的罕见病例。

The strange case of congenital mitral stenosis in an adult man with cor triatriatum.

作者信息

Burzo Maria Livia, De Matteis Giuseppe, Nicolazzi Maria Anna, Fedele Elisa, Della Polla Davide Antonio, Pennestrì Faustino, Favuzzi Angela Maria Rita

机构信息

Department of Internal Medicine, Fondazione Policlinico Universitario A.Gemelli IRCCS, Catholic University of the Sacred Heart School of Medicine, Rome, Italy.

Department of Cardiovascular Sciences, Fondazione Policlinico Universitario A.Gemelli IRCCS, Catholic University of the Sacred Heart School of Medicine, Rome, Italy.

出版信息

Echocardiography. 2019 Nov;36(11):2122-2125. doi: 10.1111/echo.14497. Epub 2019 Oct 1.

Abstract

We report the case of a 74-year-old male, with a medical history of cor triatriatum, admitted with a 10-day history of intermittent fever. Three sets of blood cultures were positive for Providencia rettgeri. Transthoracic and transesophageal echocardiogram excluded infective endocarditis, but revealed a congenital accessory tissue adhering to the mitral valve, causing supravalvular mitral stenosis. Cor triatriatum sinistrum is a rare congenital cardiac anomaly, even more uncommon in adults, and quite exceptional when associated with mitral valve disease. Because the patient had no symptoms related to the heart valve disease, no surgical indication was given and he was managed conservatively.

摘要

我们报告一例74岁男性病例,其有三房心病史,因间歇性发热10天入院。三套血培养结果显示雷特格普罗威登斯菌阳性。经胸和经食管超声心动图排除了感染性心内膜炎,但发现有一先天性附属组织附着于二尖瓣,导致二尖瓣瓣上狭窄。左位三房心是一种罕见的先天性心脏畸形,在成年人中更为少见,与二尖瓣疾病相关时则极为罕见。由于患者无与心脏瓣膜疾病相关的症状,未给予手术指征,对其进行了保守治疗。

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