Davies G, Reid L
Arch Dis Child. 1971 Oct;46(249):623-32. doi: 10.1136/adc.46.249.623.
During childhood the lung not only grows in size but alveoli and arteries multiply and the pattern of muscularity of the arteries changes. A quantitative study is here reported on 4 cases of scoliosis. The limitation and distortion of space available affect lung growth. In scoliosis, alveoli are too few in number, often emphysematous, and may even atrophy, the changes being irregularly distributed throughout a lobe or lung. Generally, the size of the large pulmonary arteries is appropriate to the lobar volume and hence small for the age of the child: arterial muscle hypertrophy and abnormal extension to the periphery were seen only in 2 of the 4 cases in which there was right ventricular hypertrophy. In these, hypoxaemia had been present for some time before death and this, not hypoplasia, seemed responsible for the muscle hypertrophy. In 2 cases where scoliosis was associated with a mesodermal dysplasia, there was an excessive number of intra-acinar arteries.
在儿童时期,肺不仅体积增大,肺泡和动脉数量增加,动脉的肌性结构也发生变化。本文报告了4例脊柱侧弯的定量研究。可用空间的限制和变形影响肺的生长。在脊柱侧弯中,肺泡数量过少,常呈肺气肿样,甚至可能萎缩,这些变化在一个肺叶或整个肺内分布不均。一般来说,大的肺动脉大小与肺叶体积相称,因此对于儿童年龄来说较小:仅在4例右心室肥大的病例中的2例中观察到动脉肌肥厚和异常向周边延伸。在这些病例中,死亡前低氧血症已存在一段时间,似乎是这种情况而非发育不全导致了肌肥厚。在2例脊柱侧弯与中胚层发育异常相关的病例中,腺泡内动脉数量过多。