论文部分内容阅读
艾布斯坦(EbStein)氏畸形合并卵园孔未闭一例,经手术证实,报告如下: 女、9岁。生后有先天性心脏病,哭时口唇发紫,曾出现过心动过速。(发育中等营养尚可)血压、脉博正常。唇及指暗红。听诊于胸骨左缘2~3肋可闻及粗糙之收缩期Ⅱ级杂者,P_2不亢进,无明显传导。触之轻度震颤。心界左侧略大。肺部无干湿罗。心电图:窦性心律,不正常心电图。(1)左前分支传导阻滞;(2)完全性右束支传导阻滞;(3)右心房增大;(4)左心室肥厚。
Ebstein (EbStein) malformations with oval hole closed a case confirmed by surgery, the report is as follows: Female, 9 years old. After birth, congenital heart disease, crying lips purple, there have been tachycardia. (Development of moderate nutrition is acceptable) Blood pressure, pulse Bo normal. Lips and fingers dark red. Auscultation on the left side of the sternum 2 ~ 3 ribs can be heard and rough systolic grade Ⅱ complex, P_2 not hyperthyroidism, no significant conduction. Touch mild tremor. Left slightly larger heart. No dry lung wet Luo. ECG: sinus rhythm, abnormal ECG. (1) left anterior branch block; (2) complete right bundle branch block; (3) right atrium enlargement; (4) left ventricular hypertrophy.