Ryland D, Reid L
Thorax. 1971 Sep;26(5):602-9. doi: 10.1136/thx.26.5.602.
Quantitative studies have, for the first time, been carried out on the single lung in a case of unilateral pulmonary aplasia, in which the other lung was represented by a rudimentary bronchial stump. The patient died at the age of 3 months. The lung was enlarged to almost twice the normal volume, filling the intrathoracic cavity. The bronchial generations were reduced in number. Pulmonary artery branches were also too few, the supernumerary being more reduced than the conventional; muscle had extended abnormally far into peripheral arteries. The alveolar number was twice the normal for one lung, that is, it represented the normal total for age; alveolar size was rather less than normal. The hypoplasia of airways and blood vessels represents an early intrauterine disturbance in lung growth, caused perhaps by the same factor that inhibited the development of the second lung; the increased alveolar multiplication probably reflects increase in available space during fetal life.
首次对单侧肺发育不全病例中的单肺进行了定量研究,该病例中另一肺由一个发育不全的支气管残端代表。患者3个月时死亡。该肺增大至几乎为正常体积的两倍,充满胸腔。支气管分支数量减少。肺动脉分支也过少,多余分支比正常分支减少得更多;肌肉异常延伸至外周动脉。肺泡数量是单肺正常数量的两倍,即代表了该年龄的正常总数;肺泡大小略小于正常。气道和血管发育不全代表肺生长早期的子宫内紊乱,可能由抑制另一肺发育的相同因素引起;肺泡增殖增加可能反映了胎儿期可用空间的增加。