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先天性二尖瓣关闭不全与主动脉缩窄。两例手术治疗报告。

Congenital mitral incompetence and coarctation of aorta. Report of two cases treated surgically.

作者信息

Terzaki A K, Leachman R D, Ali M K, Hallman G L, Cooley D A

出版信息

Thorax. 1972 Nov;27(6):729-37. doi: 10.1136/thx.27.6.729.

Abstract

Two patients with congenital mitral incompetence and coarctation of the aorta are presented. One patient had associated patent ductus arteriosus, bicuspid aortic valve, and endocardial fibroelastosis. The diagnosis in the two patients presented is well established by clinical, laboratory, and surgical findings and also by necropsy examination in one case. It is proposed that the rarity of reported cases in the literature may have resulted from the frequent diagnosis of left ventricular failure in infancy secondary to coarctation, leading to the assumption that a mitral insufficiency murmur, when present, is due to functional regurgitation. Likewise, the murmur may be mistakenly thought to originate from a ventricular septal defect. The diagnosis of coarctation of the aorta presented no problem in either patient, while detection of the mitral incompetence was difficult. Coarctation of the aorta complicated by pulmonary hypertension in the absence of intracardiac shunt should draw attention to the possibility of associated mitral incompetence. Congestive heart failure, especially after correction of coarctation, was also an indication of possible associated mitral insufficiency. The two patients were treated by repair of coarctation of the aorta at 3 months and 3 years of age and by mitral valve replacement at the age of 18 months and 5 years, respectively. One patient was in terminal heart failure and died following mitral valve surgery. The other patient benefited from the operation and her case has been followed for over one year. Correction of coarctation of the aorta provided only temporary relief of heart failure. Until both anomalies are corrected response will generally be unsatisfactory. The aetiology of combined mitral incompetence and coarctation of the aorta can be explained on a congenital basis. Endocardial fibroelastosis of the left ventricle is thought to be secondary to coarctation of the aorta, mitral incompetence, or both.

摘要

本文报告了两名患有先天性二尖瓣关闭不全和主动脉缩窄的患者。一名患者伴有动脉导管未闭、二叶式主动脉瓣和心内膜弹力纤维增生症。通过临床、实验室和手术检查结果,以及其中一例的尸检,明确了这两名患者的诊断。文献中报道的病例罕见,可能是因为婴儿期因主动脉缩窄继发左心室衰竭的诊断较为常见,导致人们认为出现的二尖瓣反流杂音是功能性反流所致。同样,该杂音可能被错误地认为源于室间隔缺损。两名患者的主动脉缩窄诊断均无问题,但二尖瓣关闭不全的检测较为困难。在无心脏内分流的情况下,主动脉缩窄并发肺动脉高压应引起对合并二尖瓣关闭不全可能性的关注。充血性心力衰竭,尤其是在主动脉缩窄矫正后,也是可能合并二尖瓣关闭不全的一个指征。两名患者分别在3个月和3岁时接受了主动脉缩窄修复术,在18个月和5岁时接受了二尖瓣置换术。一名患者在二尖瓣手术后因终末期心力衰竭死亡。另一名患者从手术中获益,其病例已随访一年多。主动脉缩窄的矫正仅暂时缓解了心力衰竭。在两种异常均得到矫正之前,总体反应通常不会令人满意。二尖瓣关闭不全合并主动脉缩窄的病因可以从先天性角度进行解释。左心室心内膜弹力纤维增生症被认为是继发于主动脉缩窄、二尖瓣关闭不全或两者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5b2/469972/0ea5fd41e412/thorax00126-0089-a.jpg

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