论文部分内容阅读
1921年Faber首次报道家族性自发性气胸,此系一临床少见的病因不明的特发性自发性气胸。本文报告一家系的3例患者。例1,男68岁,50岁时曾患支气管哮喘,58岁时发生右侧自发性气胸行胸腔引流术治疗,1988年2月21日又出现呼吸困难,X线示右肺Ⅰ度气胸,两侧下肺野内见多个囊样阴影。CT扫描右肺轻度萎缩,两肺野内多发的大泡性肺囊肿及少量胸腔积液。血液检查仅见CRP轻度增高,血清IgE及α1抗胰蛋
In 1921 Faber first reported familial spontaneous pneumothorax, which is a clinically rare idiopathic spontaneous pneumothorax. This article reports a family of 3 patients. Example 1, male 68 years old, 50 years old had bronchial asthma, 58-year-old right spontaneous pneumothorax pleural drainage occurred on February 21, 1988 again dyspnea, X-ray showed right pneumothorax Ⅰ pneumothorax, two Side of the lung field to see more than one cyst shadow. CT scan mild right atrophy of the lungs, multiple pulmonary vesicles in the lungs of the lungs and a small number of pleural effusion. Blood tests showed only a mild increase in CRP, serum IgE and α1 anti-pancreatic egg