Congenital pulmonary malformations.

IF 0.5 4区 医学 Q4 SURGERY
Ulaş Kumbasar, Serkan Uysal, Rıza Doğan
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引用次数: 0

Abstract

There are many congenital anomalies of the lung, some of which have no clinical symptoms and are detected incidentally, while others, particularly in the neonatal and infant period, are recognized by their typical signs, symptoms, and radiological appearance. Some congenital lung anomalies are so important that they can cause the death of the patient if not diagnosed and treated early. Classification of congenital lung anomalies is difficult since these anomalies may be related to the airway, arterial and venous vascular system, pulmonary parenchyma, and primitive anterior intestinal anomalies from which the lung originates, and some anomalies may have several etiologic origins. In this review, all subgroups of congenital pulmonary malformations will be discussed.

先天性肺畸形
肺部有许多先天性畸形,其中一些没有临床症状,是偶然发现的,而另一些,尤其是新生儿和婴幼儿时期的肺部畸形,则可以通过典型的体征、症状和影像学表现识别出来。有些先天性肺部异常非常重要,如果不及早诊断和治疗,可能会导致患者死亡。先天性肺畸形的分类非常困难,因为这些畸形可能与气道、动静脉血管系统、肺实质和肺起源的原始前肠畸形有关,而且有些畸形可能有多个病因起源。本综述将讨论先天性肺畸形的所有亚组。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
98
审稿时长
3-8 weeks
期刊介绍: The Turkish Journal of Thoracic and Cardiovascular Surgery is an international open access journal which publishes original articles on topics in generality of Cardiac, Thoracic, Arterial, Venous, Lymphatic Disorders and their managements. These encompass all relevant clinical, surgical and experimental studies, editorials, current and collective reviews, technical know-how papers, case reports, interesting images, How to Do It papers, correspondences, and commentaries.
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