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肺囊性腺瘤样畸形(作者译)

[Cystic adenomatoid malformation of the lung (author's transl)].

作者信息

Cobos Barroso N, Boix Ochoa J, Corominas Casaramona J M, Liñán Cortés S, Lucaya Layret J, Torán Fuentes N

出版信息

An Esp Pediatr. 1979 Jun-Jul;12(6-7):485-92.

PMID:484942
Abstract

Four cases of congenital cystic adenomatoid malformation are presented. The age of the patients ranged from 1 day to 7 years. All cases were treated surgically and 3 of them survived. The only death in the group corresponded to the neonatal case. The clinical, radiological and patological features of congenital cystic adenomatoid malformation are also reviewed. Occasionally the clinical manifestations will be hardly noticeable or non existent and the malformation may be diagnosed beyond the neonatal period in the course of a radiological examination performed as routine or because of repeated respiratory infections. Surgery is the treatment of choice. In the group of neonates where the cystic adenomatoid malformation doesn't cause respiratory difficulty the authors feel that it might be advisable to postpone surgery until a later date.

摘要

本文报告了4例先天性囊性腺瘤样畸形病例。患者年龄从1天至7岁不等。所有病例均接受了手术治疗,其中3例存活。该组中唯一的死亡病例为新生儿病例。本文还对先天性囊性腺瘤样畸形的临床、放射学及病理学特征进行了综述。偶尔,临床表现可能不明显或不存在,畸形可能在新生儿期过后,在常规进行的放射学检查过程中或因反复呼吸道感染而被诊断出来。手术是首选的治疗方法。对于囊性肺腺瘤样畸形未引起呼吸困难的新生儿组,作者认为推迟手术至日后进行可能是明智的。

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