BRONQUIECTASIAS NO FIBROSIS QUÍSTICA. DESDE LA INFANCIA A LA ADULTEZ. ENFOQUE DIAGNOSTICO Y TERAPÉUTICO
Author(s) -
Felipe Reyes C.
Publication year - 2020
Publication title -
neumología pediátrica
Language(s) - English
Resource type - Journals
eISSN - 0718-333X
pISSN - 0718-3321
DOI - 10.51451/np.v14i2.92
Subject(s) - medicine , humanities , philosophy
Bronchiectasis is a suppurative lung disease with heterogeneous phenotypic characteristics. It is defined as abnormal dilation of the bronchi, losing the existing relationship between bronchial sizes and accompanying artery. According to their form, they can be cylindrical, varicose, saccular or cystic. According to its location, they could be diffuse or localized. The diagnosis of bronchiectasis is usually suspected in patients with chronic cough, mucopurulent bronchorrea, and recurrent respiratory infections. The etiology can be varied, being able to classify in cystic fibrosis bronchiectasis, when there is cystic fibrosis transmembrane regulator (CFTR) gene mutation and not cystic fibrosis, being post infectious the most frequent. Its relationship with childhood is unknown. Severe respiratory infections can predispose in a susceptible subject the so-called theory of the "vicious circle" and the development of these. Persistent bacterial bronchitis in children has been described as a probable cause of not cystic fibrosis bronchiectasis in adults. The treatment is based on the management of symptoms and the prevention of exacerbations. The evidence is poor and many treatments are extrapolated from cystic fibrosis bronchiectasis. We are going to describe the diagnostic and therapeutic approach of non-cystic fibrosis bronchiectasis in adults.
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