Cujec B, Ulmer B, McKaigney J P, Bharadwaj B
Department of Cardiovascular Surgery, University of Saskatchewan Hospital, Saskatoon, Canada.
Ann Thorac Surg. 1987 Dec;44(6):658-9. doi: 10.1016/s0003-4975(10)62158-3.
A 25-year-old man experienced rapidly progressing Budd-Chiari syndrome. Despite extensive radiological investigations, no atrial mass could be identified. At operation, a right atrial myxoma was found that originated from the eustachian valve and prolapsed into the inferior vena cava. Following successful removal of the myxoma, the ascites and peripheral edema resolved completely. Right atrial myxoma is a rare cardiac tumor that may present with embolic, obstructive, or constitutional signs and symptoms and is a potentially curable cause of Budd-Chiari syndrome.
一名25岁男性患快速进展性布加综合征。尽管进行了广泛的影像学检查,但未发现心房肿物。手术时发现一个起源于欧氏瓣并脱垂至下腔静脉的右房黏液瘤。成功切除黏液瘤后,腹水和外周水肿完全消退。右房黏液瘤是一种罕见的心脏肿瘤,可表现为栓塞、梗阻或全身症状体征,是布加综合征潜在的可治愈病因。