Lung Agenesis: An Embryological Perspective

N. Hayati, M. B. E. Susyanto
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Abstract

Lung agenesis or aplasia is a very rare congenital anomaly. It is estimated at 34 per million live births. The etiology of this disorder has not been clearly known. Failure of development of the primitive lung bud leads is the cause of this condition. In half of these cases, it has been reported in association with other congenital defects such as congenital malformation of the cardio-vascular, skeletal, gastrointestinal or genitor-urinary system. This condition is usually diagnosed during childhood. Some patients with lung agenesis may suffer from recurrent respiratory distress, dyspnea, and lung infections. We report a case of a 1-month 28 day old male infant with right-sided lung agenesis association with spina bifida as other congenital defects presented to us with recurrent severe respiratory distress. The purpose of writing this case report is to explore a case of pulmonary agenesis in terms of its embryological aspects.
肺发育不全:胚胎学观点
肺发育不全是一种非常罕见的先天性异常。据估计,每百万活产婴儿中有34例死亡。这种疾病的病因尚不清楚。原始肺芽导的发育失败是造成这种情况的原因。据报道,在这些病例的一半中,它与其他先天性缺陷有关,如心血管、骨骼、胃肠道或生殖泌尿系统的先天性畸形。这种情况通常在儿童时期被诊断出来。一些肺发育不全的患者可能会出现反复的呼吸窘迫、呼吸困难和肺部感染。我们报告一例1个月28天大的男婴右肺发育不全与脊柱裂相关,其他先天性缺陷呈现给我们复发性严重呼吸窘迫。撰写此病例报告的目的是探讨一例肺发育不全在其胚胎学方面。
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