Goldstein J D, Rabinovitch M, Van Praagh R, Reid L
Am J Cardiol. 1979 May;43(5):962-8. doi: 10.1016/0002-9149(79)90360-6.
A unique case of pulmonary vascular anomalies causing persistent pulmonary hypertension in a newborn is described. The child died 3 days after birth. Necropsy revealed marked hypoplasia of the right and left pulmonary arteries with a normal main pulmonary artery, patent ductus arteriosus, bilateral systemic arteries to the lungs from the abdominal aorta, and partial anomalous pulmonary venous connection. Quantitative morphometric techniques demonstrated slight abnormalities of alveolar development and severe arterial medial hypertrophy with abnormal extension of muscle into small peripheral arteries. Bronchopulmonary development appeared relatively normal in spite of the vascular abnormalities.
本文描述了一例因肺血管异常导致新生儿持续性肺动脉高压的独特病例。患儿出生后3天死亡。尸检显示左右肺动脉明显发育不全,主肺动脉正常,动脉导管未闭,腹主动脉发出双侧体动脉至肺部,以及部分肺静脉异位连接。定量形态计量学技术显示肺泡发育略有异常,动脉中层严重肥厚,肌肉异常延伸至外周小动脉。尽管存在血管异常,但支气管肺发育相对正常。