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支气管肺发育不良:坏死性细支气管炎和肺纤维化的肺部病理后遗症。

Bronchopulmonary dysplasia: the pulmonary pathologic sequel of necrotizing bronchiolitis and pulmonary fibrosis.

作者信息

Bonikos D S, Bensch K G, NORTHWAY W H, Edwards D K

出版信息

Hum Pathol. 1976 Nov;7(6):643-66. doi: 10.1016/s0046-8177(76)80077-9.

Abstract

A light and electron microscopic study was carried out in 21 infants in whom the pathologic diagnosis of bronchopulmonary dysplasia had been made. All the infants except two had the respiratory distress syndrome at birth, and all 21 had been treated with respirator and oxygen therapy for various periods of time. The pathologic alterations observed in all the infants studied were primarily damage of the bronchial and bronchiolar ciliary apparatus and mucous membranes, severe necrotizing bronchiolitis, and marked bronchiolar and alveolar fibrosis. These changes were more pronounced in infants who survived the longest period of time. Such inflammatory and fibrotic changes are known to predispose to destruction of lung tissue, emphysema, and pulmonary hypertension. Six of these 21 infants developed symptoms and signs of cardiac atrial or ventricular stress, including cor pulmonale, prior to their demise. These infants were among those that survived the longest periods of time, had the longest exposure to supplemental oxygen, and showed histopathologically severe pulmonary fibrosis and emphysema.

摘要

对21例已做出支气管肺发育不良病理诊断的婴儿进行了光镜和电镜研究。除2例婴儿外,其余所有婴儿出生时均患有呼吸窘迫综合征,并且所有21例婴儿都接受了不同时长的呼吸机和氧气治疗。在所有研究的婴儿中观察到的病理改变主要是支气管和细支气管纤毛装置及黏膜的损伤、严重的坏死性细支气管炎以及明显的细支气管和肺泡纤维化。这些变化在存活时间最长的婴儿中更为明显。已知此类炎症和纤维化变化易导致肺组织破坏、肺气肿和肺动脉高压。这21例婴儿中有6例在死亡前出现了心脏心房或心室应激的症状和体征,包括肺心病。这些婴儿是存活时间最长、接受补充氧气时间最长且组织病理学显示有严重肺纤维化和肺气肿的婴儿。

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