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持续性局限性肺间质肺气肿与淋巴管扩张:存在因果关系吗?

Persistent localized pulmonary interstitial emphysema and lymphangiectasia: a causal relationship?

作者信息

Leonidas J C, Bhan I, McCauley R G

出版信息

Pediatrics. 1979 Aug;64(2):165-71.

PMID:471606
Abstract

The mechanism responsible for persistent regional pulmonary interstitial emphysema under tension, which occasionally complicates assisted ventilation, has not been explained. It is difficult to comprehend how interstitial air may cause lobar hyperinflation and not escape to the mediastinum or pleura. Histologic examination of resected emphysematous lung in two neonates with this type of interstitial emphysema revealed air dissecting from the interstitial connective tissue into markedly dilated lymphatics. It is proposed that intralymphatic air dissection causing emphysematous lymphangiectasia may be responsible for fixation of the lung in the emphysematous state.

摘要

张力性持续性局部肺间质气肿的机制尚未得到解释,这种情况偶尔会使辅助通气变得复杂。很难理解间质内的气体如何导致肺叶过度膨胀而不逸出至纵隔或胸膜。对两名患有此类间质气肿的新生儿切除的气肿肺进行组织学检查发现,气体从间质结缔组织进入明显扩张的淋巴管。有人提出,导致气肿性淋巴管扩张的淋巴管内气体剥离可能是肺处于气肿状态的原因。

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