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三房心:被复杂先天性心脏畸形所掩盖。

Cor triatriatum: masked by complex congenital cardiac anomalies.

作者信息

Nudel D B, Kelley M J, Hellenbrand W E, Barash P, Stansel H C, Berman M A

出版信息

J Thorac Cardiovasc Surg. 1976 Oct;72(4):644-51.

PMID:966800
Abstract

The radiographic, angiographic, hemodynamic, and surgical features of 2 cases of cor triatriatum complicated by other cardiac anomalies are presented. In the first case, the patient had tetralogy of Fallot, the scimitar syndrome, and left ventricular obstruction. In the second case the patient had truncus arteriosus. The first case was revealed only after augmentation of pulmonary flow by an aorta-pulmonary artery anastomosis. In the second case, the diagnosis was retrospectively suggested by certain angiographic and hemodynamic clues. The prospective diagnosis was made only after a modified Rastelli procedure for truncus arteriosus. The difficulties encountered in making the diagnosis in both cases are discussed. It is stressed that a high index of suspicion, thorough accumulation and examination of hemodynamic data, and excellent angiograms and plain film radiography are all necessary to an early diagnosis of cor triatriatum when the latter is complicated by other congenital heart anomalies.

摘要

本文介绍了2例合并其他心脏异常的三房心患者的影像学、血管造影、血流动力学及手术特征。第一例患者患有法洛四联症、弯刀综合征及左心室梗阻。第二例患者患有共同动脉干。第一例仅在通过主动脉-肺动脉吻合术增加肺血流量后才得以发现。第二例则是通过某些血管造影和血流动力学线索进行回顾性诊断提示。仅在进行改良的共同动脉干Rastelli手术后才做出前瞻性诊断。文中讨论了两例诊断过程中遇到的困难。强调当三房心合并其他先天性心脏异常时,高度的怀疑指数、全面收集和检查血流动力学数据以及高质量的血管造影和X线平片对早期诊断三房心均十分必要。

相似文献

1
Cor triatriatum: masked by complex congenital cardiac anomalies.三房心:被复杂先天性心脏畸形所掩盖。
J Thorac Cardiovasc Surg. 1976 Oct;72(4):644-51.
2
Cor triatriatum: angiographic diagnosis by retrograde catheterization of the dorsal accessory chamber.
Br J Radiol. 1971 Apr;44(520):273-6. doi: 10.1259/0007-1285-44-520-273.
3
Cor triatriatum: preoperative diagnosis and successful surgical repair in a small infant.
J Pediatr. 1967 Dec;71(6):840-7. doi: 10.1016/s0022-3476(67)80009-x.
4
Successful management of cor triatriatum associated with anomalous pulmonary/systemic venous connection in an infant.成功治疗婴儿合并异常肺/体静脉连接的三房心。
Pediatr Cardiol. 1982;2(4):319-22. doi: 10.1007/BF02426981.
5
Cor triatriatum. Total correction in an infant.三房心。婴儿期的根治性手术。
J Thorac Cardiovasc Surg. 1968 Jul;56(1):114-9.
6
Cor triatriatum. Successful correction in 4 patients including 2 less than 1 year of age.三房心。4例患者成功矫正,其中2例年龄小于1岁。
Ann Thorac Surg. 1974 Apr;17(4):325-31. doi: 10.1016/s0003-4975(10)65659-7.
7
[Cor triatriatum associated with a ventricular septal defect in infancy. 2 cases treated surgically].[婴儿期三房心合并室间隔缺损。2例手术治疗]
Arch Mal Coeur Vaiss. 1978 Sep;71(9):1070-5.
8
Cor triatriatum and total anomalous pulmonary venous connection: a rare, surgically correctable anomaly.三房心与完全性肺静脉异位连接:一种罕见的、可手术矫正的异常情况。
J Thorac Cardiovasc Surg. 1985 Sep;90(3):443-5.
9
Subtotal cor triatriatum with left partial anomalous pulmonary venous return. Successful surgical repair in an infant.部分三房心合并左肺静脉部分异位引流。婴儿成功接受手术修复。
J Thorac Cardiovasc Surg. 1977 Sep;74(3):461-6.
10
Cor triatriatum associated with unilateral anomalous pulmonary venous drainage in an infant.婴儿三尖瓣闭锁合并单侧肺静脉异位引流
Aust Paediatr J. 1981 Jun;17(2):122-4. doi: 10.1111/j.1440-1754.1981.tb01919.x.

引用本文的文献

1
Cor triatriatum in an adult with mitral regurgitation and massive left atrial enlargement.一名患有二尖瓣反流和巨大左心房扩大的成年患者的三房心。
Cardiovasc Intervent Radiol. 1983;6(1):37-40. doi: 10.1007/BF02552790.