Eichelberger M R, Kettrick R G, Hoelzer D J, Swedlow D B, Schnaufer L
J Pediatr Surg. 1980 Aug;15(4):395-7. doi: 10.1016/s0022-3468(80)80742-1.
Agenesis of the hemidiaphragm is an unusual congenital anomaly associated with a high mortality. This paper presents the fourth patient to survive the neonatal period with agenesis of the hemidiaphragm. He was an identical twin, weighing 1.5 kg and his clinical course was characterized by ipsilateral pulmonary hypoplasia, large alveolar-arterial gradient for oxygen, persistent fetal circulatory pattern and ventilator dependence. These abnormalities suggest a pathophysiology similar to that observed in patients with Bochdalek hernia. The surgical correction, postoperative care and observation of pulmonary function following repair of agenesis of the left diaphragm are described.
半侧膈肌缺如是一种罕见的先天性异常,与高死亡率相关。本文介绍了第四例存活至新生儿期的半侧膈肌缺如患者。他是一对同卵双胞胎,体重1.5千克,其临床病程特点为同侧肺发育不全、氧的肺泡-动脉梯度大、持续胎儿循环模式和依赖呼吸机。这些异常提示其病理生理学与Bochdalek疝患者相似。本文描述了左侧膈肌缺如修补术后的手术矫正、术后护理及肺功能观察。