Eterovic Ivo, Angelini Paolo, Leachman Robert, Cooley Denton A.
Department of Surgery and the Department of Cardiology, Texas Heart Institute of St. Luke's Episcopal and Texas Children's Hospitals, Houston, Texas.
Cardiovasc Dis. 1979 Mar;6(1):66-75.
Restrictive cardiomyopathies have been variously classified and interpreted. Although their etiologic and anatomic features may vary, their common denominator is indicated by restrictive hemodynamic behavior of either the left or right ventricle or both. This report describes a case in which such restriction was caused by obliterative endomyocardial fibrosis of unknown etiology. Because of significant symptomatology, including congestive failure and syncope, the patient underwent surgical excision of the endomyocardial overgrowth.
限制型心肌病有着多种不同的分类和解读。尽管它们的病因和解剖特征可能各不相同,但其共同特征表现为左心室或右心室或两者的血流动力学受限。本报告描述了一例由病因不明的闭塞性心内膜纤维化导致这种血流动力学受限的病例。由于出现了包括充血性心力衰竭和晕厥在内的明显症状,该患者接受了心内膜过度增生的手术切除。