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先天性膈疝修补术后持续存在的肺发育不全

Persistent hypoplasia of the lung after repair of congenital diaphragmatic hernia.

作者信息

Hislop A, Reid L

出版信息

Thorax. 1976 Aug;31(4):450-5. doi: 10.1136/thx.31.4.450.

Abstract

Quantitative analysis has been used to assess growth in a lung from an infant aged 21/2 months in whom a diaphragmatic hernia was repaired at birth. The lungs had been abnormally small at birth but at 21/2 months were of normal volume. Alveoli had multiplied at the normal rate after birth but had not reached the number normal of age. The number per acinus was normal but the alveoli were increased in size, particularly in the left lung. The airway number, and thus alveolar, acinar, and arterial number, were all reduced in both lungs, the ipsilateral being most affected. The pulmonary blood vessels in both lungs showed an increased muscularity that did not correlate with lung volume or alveolar number, a feature that may have been present at birth. The degrees of hypoplasia in the two lungs were different at birth and this difference had been maintained. The effect of the disturbance to lung growth on the functioning of the lung is discussed.

摘要

定量分析已被用于评估一名出生时患有膈疝并在2个半月大时接受修复手术的婴儿肺部的生长情况。该婴儿出生时肺部异常小,但在2个半月时体积正常。出生后肺泡以正常速率增殖,但未达到该年龄的正常数量。每个腺泡的数量正常,但肺泡尺寸增大,尤其是左肺。两肺的气道数量以及因此的肺泡、腺泡和动脉数量均减少,患侧受影响最大。两肺的肺血管显示出肌层增厚,这与肺体积或肺泡数量无关,这一特征可能在出生时就已存在。两肺发育不全的程度在出生时就不同,且这种差异一直存在。文中讨论了肺部生长紊乱对肺功能的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d85/470458/adfb065e6b42/thorax00148-0087-a.jpg

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