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需要肺叶切除术的肺间质性肺气肿。辅助通气的并发症。

Pulmonary interstitial emphysema requiring lobectomy. Complications of assisted ventilation.

作者信息

Drew J H, Landau L I, Acton C M, Kent M, Campbell P E

出版信息

Arch Dis Child. 1978 May;53(5):424-6. doi: 10.1136/adc.53.5.424.

Abstract

An infant with hyaline membrane disease treated with intermittent positive pressure ventilation developed pulmonary interstitial emphysema localised to one lobe after collapse of the affected lobe. The development of tension and further symptoms necessitated lobectomy, after which the infant became totally asymptomatic. Microscopy of the resected lobe showed the unusual feature of giant cells lining the air-containing cysts. The presence of these multinucleate cells suggested the cysts may have represented greatly dilated lymphatic channels resulting from rupture of gases into the pulmonary lymphatics.

摘要

一名患有透明膜病的婴儿接受间歇性正压通气治疗后,在患侧肺叶萎陷后出现局限于一个肺叶的肺间质肺气肿。由于张力的发展和进一步的症状,需要进行肺叶切除术,术后婴儿完全无症状。对切除肺叶的显微镜检查显示,含气囊肿内衬有巨细胞这一不寻常特征。这些多核细胞的存在表明,囊肿可能代表因气体进入肺淋巴管破裂而导致的极度扩张的淋巴管。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6542/1544911/e7ab5499592e/archdisch00805-0077-a.jpg

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