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与肺发育不全相关的异常情况。

Anomalies associated with pulmonary hypoplasia.

作者信息

Page D V, Stocker J T

出版信息

Am Rev Respir Dis. 1982 Feb;125(2):216-21. doi: 10.1164/arrd.1982.125.2.216.

Abstract

We reviewed the records of 756 consecutive newborns autopsied over a 10-yr period. Using published standards for normal lung weights, low lung weight for total body weight was determined to be a reasonable estimate of pulmonary hypoplasia. Seventy-seven infants with pulmonary hypoplasia were identified. Multiple congenital malformation syndromes were found in the majority of infants with pulmonary hypoplasia. These included major diaphragmatic anomalies, renal anomalies, chromosomal disorders, extralobar pulmonary sequestration, severe musculoskeletal disorders, and isolated right-sided cardiac lesions. Ten infants had no known associated anomalies. The various theories of pathogenesis of pulmonary hypoplasia are reviewed and the suggestion is made that the cause of pulmonary hypoplasia in newborns may well be multifactorial. Various theories of pathogenesis are discussed ranging from an actual lack of space for the lungs to grow, to the possible necessity for appropriate respiratory movement during intrauterine life, to the possibility, particularly in the case of Potter's syndrome, of a primary mesodermal defect affecting multiple organ systems.

摘要

我们回顾了连续10年期间接受尸检的756例新生儿的记录。采用已发表的正常肺重量标准,确定低肺重量与总体重之比是肺发育不全的合理估计指标。共识别出77例肺发育不全的婴儿。大多数肺发育不全的婴儿患有多种先天性畸形综合征。这些综合征包括主要的膈异常、肾异常、染色体疾病、肺叶外隔离症、严重的肌肉骨骼疾病以及孤立性右侧心脏病变。10例婴儿无已知的相关异常。本文回顾了肺发育不全发病机制的各种理论,并提出新生儿肺发育不全的原因很可能是多因素的。讨论了各种发病机制理论,从肺部实际缺乏生长空间,到宫内生活期间适当呼吸运动的可能必要性,再到特别是在波特综合征的情况下,影响多个器官系统的原发性中胚层缺陷的可能性。

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