Sahin Tayfun, Bildirici Ulaş, Kandemir Caglayan, Celikyurt Umut, Ural Dilek, Komsuoglu Baki
Int J Cardiol. 2008 Jul 21;127(3):e129-31. doi: 10.1016/j.ijcard.2007.04.132. Epub 2007 Aug 10.
Cor triatriatum dextrum is a rare congenital malformation, usually associated with complex right heart abnormalities, characterized by a membrane that divides the right atrium into two chambers. It is considered the result of the incomplete and abnormal regression of the embryonic right valve of the sinus venosus. With an incomplete regression, a fenestrated or an unfenestrated membrane may persist in the right atrium. Cor triatriatum dextrum may be seen with congenital cardiac defects associated with the right heart. We have diagnosed infective endocarditis in a 19 year old male patient with asymptomatic incomplete cor triatriatum dextrum, PFO and valvular-infundibular severe pulmonary stenosis based on the Duck criteria, with a positive blood culture and 3 minor criteria. Echocardiography did not reveal any vegetations. Antibiotherapy was given and then regions responsible of the stenosis were resected surgically. After surgery a small outlet type VSD development was observed.
右三房心是一种罕见的先天性畸形,通常与复杂的右心异常相关,其特征是有一个将右心房分为两个腔室的隔膜。它被认为是胚胎期静脉窦右瓣膜不完全和异常退化的结果。由于退化不完全,右心房可能会残留有孔或无孔的隔膜。右三房心可能与右心相关的先天性心脏缺陷同时出现。我们根据杜克标准,在一名19岁男性患者中诊断出感染性心内膜炎,该患者有无症状的不完全性右三房心、卵圆孔未闭和瓣膜-漏斗部重度肺动脉狭窄,血培养阳性且有3项次要标准。超声心动图未发现任何赘生物。给予抗生素治疗,然后手术切除导致狭窄的区域。术后观察到一个小的流出道型室间隔缺损。