Andersen K, Myhre E S, Smith G
Medisinsk avdeling, Regionsykehuset i Tromsø.
Tidsskr Nor Laegeforen. 1993 Oct 10;113(24):3025-7.
Cor triatriatum is a rare congenital heart disease. In its classic form its consists of a fibromuscular perforated membrane which divides the left atrium and obstructs blood flow from pulmonary veins to mitral orifice. Clinical symptoms and signs resemble those of mitral stenosis. Traditionally cor triatriatum was encountered most often in infancy and childhood. We describe the case of a young man with cor triatriatum and atrial fibrillation, with syncope. He was operated on with total resection of the obstructing membrane. Modern echocardiography has made diagnosis more easy. Thus, an increasing number of cases of cor triatriatum are diagnosed in adults with few or no symptoms. Symptoms, diagnosis and treatment are discussed, with emphasis on these patients.
三房心是一种罕见的先天性心脏病。其典型形式是由一层纤维肌性穿孔膜将左心房分隔开,并阻碍肺静脉血液流向二尖瓣口。临床症状和体征与二尖瓣狭窄相似。传统上,三房心最常见于婴儿期和儿童期。我们描述了一例患有三房心并伴有房颤及晕厥的青年男性病例。他接受了阻塞膜完全切除术。现代超声心动图使诊断更加容易。因此,越来越多无症状或症状轻微的三房心病例在成人中被诊断出来。本文将讨论其症状、诊断和治疗,重点关注这类患者。