家族性先天性心脏病2例

• 作 者: 党延琴 党双培
• 机 构: 长庆石油勘探局职工医院,长庆石油勘探局职工医院
• 出 处: 陕西医学杂志
• 发表日期: 1993年09期
• 关键词: 先天性心脏病 室间隔缺损 心尖搏动 口周发绀 第一心音 收缩期杂音 族性 前区 生长发育 间书

例1 男,4岁.因自幼活动后气急、口周发绀来诊.查体:生长发育较同龄儿落后,口周略紫,心前区隆起,心尖搏动弥散,心界向两侧中度扩大,胸骨左缘第3、4肋间可闻及Ⅲ级粗糙的收缩期杂音并掩盖第一心音,杂音向左腋下传导且触到震颤.经胸部X 线透视、拍片、心电图及B 超检查,均证实为先天性心脏病、室间隔缺损.例2 男,2岁,例1之胞第。症状与例1相同,以

Case 1 male, 4 years old .Because of childhood activity after the shortness of breath, perioral cyanosis to the clinic .Check the body: growth and development more than the same age children lameness, perioral purple, apical area uplift, apex beating dispersion, the heart bound to both sides Degree of expansion, the left border of the sternum 3,4 intercostal can be heard and Ⅲ rough systolic murmur and cover the first heart sound, murmur conduction to the left armpit and touch tremor.Through the chest X-ray, film, ECG and B-ultrasound, were confirmed as congenital heart disease, ventricular septal defect .Example 2 male, 2 years old, the first case of cell number. The same symptoms as in Example 1