Voigtländer T, Nowak B, Eckhardt D, Becker H J, Satter P
Medizinische Klinik I, Stadtkrankenhaus Hanau, Internistische Gemeinschaftspraxis Offenbach, Waldstrasse.
Z Kardiol. 1994 Sep;83(9):605-9.
The cor triatriatum sinistrum is a rare congenital malformation. Frequently, the patients become symptomatic in infancy with clinical signs of severe congestive heart failure. We report on an adult patient with only mild symptoms with cor triatriatum sinistrum and atrial septal defect. The embryological basis of the disorder and the hemodynamic conditions which permitted this patient to remain symptom free for a long period are discussed.
左房三房心是一种罕见的先天性畸形。患者通常在婴儿期出现症状,伴有严重充血性心力衰竭的临床体征。我们报告一例成年左房三房心合并房间隔缺损患者,仅有轻微症状。本文讨论了该疾病的胚胎学基础以及使该患者长期无症状的血流动力学状况。