Congenital pulmonary airway malformation

Česká verzia

Authors: J. Micherová ¹; P. Rejtar ²; B. Frýbová ³; Hubert Vaníček ¹
Authors place of work: Dětská klinika LF a FN Hradec Králové ¹; Radiologická klinika LF a FN Hradec Králové ²; Klinika dětské chirurgie 2. LF UK a FN Motol, Praha ³
Published in the journal: Čes-slov Pediat 2021; 76 (5): 240-245.
Category: Original Papers

Summary

Congenital pulmonary airway malformation (CPAM) with its incidence 1:25–35 000 belongs to the most frequent congenital lung anomalies. Pulmonary sequestration (PS) occures less often. These malformations can be mixed sometimes, called hybrid lesions. They need to be correctly diagnosed in patients with unknown pulmonary lesions of any age. They can be easily diagnosed prenatally by ultrasonography. Clinical presentation differs from asymptomatic lesions to respiratory failure of child. Therapeutic approach depends on symptomps, size and type of the malformation as well as personal experience.

Keywords:

congenital pulmonary airway malformation – CPAM – congenital cystic adenomatoid malformation – CCAM – congenital thoracic malformation – CTM – congenital lung masses – CLM – bronchopulmonary sequestration – PS

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