Childhood Interstitial Lung Disease

被引:6
作者
Buyuksahin, Halime Nayir [1 ,2 ]
Kiper, Nural [1 ]
机构
[1] Hacettepe Univ, Ihsan Dogramaci Childrens Hosp, Sch Med, Dept Pediat Pulmonol, Ankara, Turkiye
[2] Hacettepe Univ, Ihsan Dogramaci Childrens Hosp, Sch Med, Dept Pediat Pulmonol, TR-06100 Ankara, Turkiye
关键词
children; interstitial; lung disease; computed tomography; genetic tests; PULMONARY ALVEOLAR MICROLITHIASIS; NEUROENDOCRINE CELL HYPERPLASIA; HYPERSENSITIVITY PNEUMONITIS; BRONCHOALVEOLAR LAVAGE; GENETIC-DISORDERS; CLINICAL-COURSE; YOUNG-CHILDREN; FOLLOW-UP; DIAGNOSIS; CLASSIFICATION;
D O I
10.1089/ped.2022.0013
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Childhood interstitial lung disease (chILD) is a heterogeneous group of diseases with various clinical and imaging findings. The incidence and prevalence have increased in recent years, probably due to better comprehension of these rare diseases and increased awareness among physicians. chILDs present with nonspecific pulmonary symptoms, such as tachypnea, hypoxemia, cough, rales, and failure to thrive. Unnecessary invasive procedures can be avoided if specific mutations are detected through genetic examinations or if typical imaging patterns are recognized on computed tomography. Disease knowledge and targeted therapies are improving through international collaboration. Pulmonary involvement in systemic diseases is not uncommon. Pulmonary involvement may be the first finding in connective tissue diseases. This review aims to present a systematic patient-targeted approach to the diagnosis of chILD.
引用
收藏
页码:5 / 15
页数:11
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