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三尖瓣闭锁是一种少见的先天性心脏畸形,国内外仅有少数病例报告。我院仅发现一例,其临床及X线资料较为典型,经心血管造影证实,并经阜外医院放射线科会诊,现报告如下: [病例] 患儿男性,10岁。患者自幼易感冒,活动后出现心悸气短、紫绀并喜蹲踞。查体:体温36℃,脉搏120次,呼吸20次,血压90/60mmHg。发育中等,营养欠佳,有紫绀及杵状指趾。心界稍大,胸骨左缘可扪及震颤,并可听到Ⅳ级收缩期杂音。化验:血红蛋白12g,红细胞600万,白细胞7,000。心电
Tricuspid atresia is a rare congenital heart disease, only a few cases at home and abroad reported. Our hospital found only one case, the clinical and X-ray data is more typical, confirmed by cardiovascular angiography, and by the Fu Wai Hospital Radiological consultation, are as follows: [Case] children male, 10 years old. Easy to catch cold since childhood, after the event of palpitation shortness of breath, cyanosis and hi squatting. Physical examination: body temperature 36 ℃, pulse 120 times, breathing 20 times, blood pressure 90 / 60mmHg. Moderately developed, poor nutrition, cyanosis and clubbing toe. Slightly larger heart, sternal left palpable palpable tremor, and can hear Ⅳ systolic murmur. Laboratory tests: hemoglobin 12g, 6 million red blood cells, white blood cells 7,000. ECG