Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 1. Introduction / 결핵
Tuberculosis and Respiratory Diseases
; : 269-276, 2019.
Article
em En
| WPRIM
| ID: wpr-761966
Biblioteca responsável:
WPRO
ABSTRACT
Idiopathic interstitial pneumonia (IIP) is a histologically identifiable pulmonary disease without a known cause that usually infiltrates the lung interstitium. IIP is largely classified into idiopathic pulmonary fibrosis, idiopathic non-specific interstitial pneumonia, respiratory bronchiolitis-interstitial lung disease (ILD), cryptogenic organizing pneumonia, desquamative interstitial pneumonia, and acute interstitial pneumonia. Each of these diseases has a different prognosis and requires specific treatment, and a multidisciplinary approach that combines chest high-resolution computed tomography (HRCT), histological findings, and clinical findings is necessary for their diagnosis. Diagnosis of IIP is made based on clinical presentation, chest HRCT findings, results of pulmonary function tests, and histological findings. For histological diagnosis, video-assisted thoracoscopic biopsy and transbronchial lung biopsy are used. In order to identify ILD associated with connective tissue disease, autoimmune antibody tests may also be necessary. Many biomarkers associated with disease prognosis have been recently discovered, and future research on their clinical significance is necessary. The diagnosis of ILD is difficult because patterns of ILD are both complicated and variable. Therefore, as with other diseases, accurate history taking and meticulous physical examination are crucial.
Palavras-chave
Texto completo:
1
Base de dados:
WPRIM
Assunto principal:
Exame Físico
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Prognóstico
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Testes de Função Respiratória
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Tórax
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Biópsia
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Biomarcadores
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Classificação
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Doenças Pulmonares Intersticiais
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Pneumonia em Organização Criptogênica
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Doenças do Tecido Conjuntivo
Tipo de estudo:
Diagnostic_studies
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Guideline
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Prognostic_studies
Idioma:
En
Ano de publicação:
2019
Tipo de documento:
Article