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先天性肺叶气肿和先天性囊性腺瘤样畸形肺叶切除术后的肺功能。一项随访研究。

Pulmonary function after lobectomy for congenital lobar emphysema and congenital cystic adenomatoid malformation. A follow-up study.

作者信息

Frenckner B, Freyschuss U

出版信息

Scand J Thorac Cardiovasc Surg. 1982;16(3):293-8. doi: 10.3109/14017438209101066.

Abstract

Eight patients with congenital lobar emphysema and eight with congenital cystic adenomatoid malformations were operated upon between 1970 and 1978. A lobectomy was performed in all cases. At follow-up after 3 to 11 years all of the patients without concomitant disease or malformations were subjectively well with a physical performance equal to those of their playmates. Lung function tests indicated lung volumes of about 90% of predicted normal values, indicating some compensatory growth of the remaining lung tissue. Functional impairment owing to loss of lung tissue or residual disease was ruled out by the existence of a normal working capacity and maintenance of the alveolar gas exchange during intense exercise.

摘要

1970年至1978年间,对8例先天性大叶性肺气肿患者和8例先天性囊性腺瘤样畸形患者进行了手术。所有病例均行肺叶切除术。在3至11年的随访中,所有无伴随疾病或畸形的患者主观感觉良好,体能与同龄人相当。肺功能测试显示肺容积约为预测正常值的90%,表明剩余肺组织有一定的代偿性生长。由于正常工作能力的存在以及剧烈运动期间肺泡气体交换的维持,排除了因肺组织丧失或残留疾病导致的功能损害。

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