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“获得性”大叶性肺气肿:早产儿呼吸窘迫的一种并发症。

"Acquired" lobar emphysema: a complication of respiratory distress in premature infants.

作者信息

Cooney D R, Menke J A, Allen J E

出版信息

J Pediatr Surg. 1977 Dec;12(6):897-904. doi: 10.1016/0022-3468(77)90599-1.

Abstract

Ten premature infants with respiratory distress developed a type of pulmonary lobar emphysema that is clinically and histologically distinct from interstitial or congenital lobar emphysema. In eight patients emphysema was noted in the right lower lobe, while in two the left upper lobe was affected. Five infants exhibited nonresolution of the emphysema and an inability to be weaned from ventilator support. Lung scans in these five infants showed absent or markedly decreased perfusion of the involved lobe. Lobectomy was necessary. Postoperatively, their respiratory status improved and they were successfully weaned from the ventilator. Five premature infants with identical radiographic emphysematous changes had normal lung scans. These infants did not require lobectomy and were also successfully weaned from the ventilator. Radiographic changes of lobar emphysema in these five infants completely resolved. Pathologic changes in the excised lobes were characteristic of bronchopulmonary dysplasia and obstructive intraalveolar emphysema. The long-term effects of positive pressure ventilation, oxygen, and suctioning techniques directed toward the right lower lobe may play an important role in the etiology of "acquired" lobar emphysema.

摘要

十名患有呼吸窘迫的早产儿出现了一种肺叶气肿,其在临床和组织学上与间质性或先天性肺叶气肿不同。八名患者的右下叶出现气肿,两名患者的左上叶受到影响。五名婴儿的气肿未消退,无法撤掉呼吸机支持。这五名婴儿的肺部扫描显示受累肺叶灌注缺失或明显减少。需要进行肺叶切除术。术后,他们的呼吸状况改善,成功撤掉了呼吸机。另外五名有相同影像学气肿改变的早产儿肺部扫描正常。这些婴儿不需要进行肺叶切除术,也成功撤掉了呼吸机。这五名婴儿的肺叶气肿影像学改变完全消退。切除肺叶的病理变化是支气管肺发育不良和阻塞性肺泡气肿的特征。针对右下叶的正压通气、吸氧和吸引技术的长期影响可能在“获得性”肺叶气肿的病因中起重要作用。

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