Milović I, Oluić D
Institute for Mother and Child Health Protection, Belgrade.
Srp Arh Celok Lek. 1992 Sep-Oct;120(9-10):301-3.
Congenital cysts of the lung originate from embryological malformation of the lung bud and usually produce clinical signs in the first months of life by expansion, causing respiratory distress, or by infection through its bronchial communication. We report a rare case of solitary congenital lung cyst in the middle lobe which was diagnosed in the 3rd month of life and remained silent until the 7th year when tension pneumothorax developed from rupture of the rapidly expanding cyst. An urgent lobectomy of the involved lobe was performed. This rare case supports the attitude that every congenital cyst of the lung should be excised as soon as the correct diagnosis is established in order to prevent serious complications.
先天性肺囊肿起源于肺芽的胚胎发育畸形,通常在出生后的头几个月因囊肿扩张产生临床症状,导致呼吸窘迫,或通过与支气管相通而发生感染。我们报告一例罕见的中叶孤立性先天性肺囊肿病例,该病例在出生后第3个月被诊断出,直至7岁时,快速扩张的囊肿破裂导致张力性气胸才出现症状。遂对受累肺叶进行了紧急肺叶切除术。这个罕见病例支持这样一种观点,即一旦确诊为先天性肺囊肿,应尽快切除,以预防严重并发症。