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Update in Diagnosis of Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormality

Nam BD, Hwang JH

Idiopathic pulmonary fibrosis (IPF), based on the 2018 international clinical practice guidelines, can be diagnosed with a usual interstitial pneumonia (UIP) pattern on high-resolution computed tomography (HRCT) and compatible clinical...
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Pleuroparenchymal fibroelastosis in Korean patients: clinico-radiologic-pathologic features and 2-year follow-up

Lee JH, Chae EJ, Song JS, Kim M, Song JW

Background/Aims: Pleuroparenchymal fibroelastosis (PPFE) is a type of rare idiopathic interstitial pneumonia that is characterized by predominantly upper lobe involvement with pleural fibrosis and subjacent parenchymal fibrosis. This study aimed...
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Diagnosis and treatment of interstitial lung disease: focusing on idiopathic pulmonary fibrosis

Kang HR, Choi SM

Interstitial lung disease (ILD) is a rare condition characterized by extensive inflammation and fibrosis mainly involving the pulmonary interstitium or alveoli. Usually, patients with ILD clinically present with chronic cough...
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Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 3. Idiopathic Nonspecific Interstitial Pneumonia

Lee J, Kim YH, Kang JY, Jegal Y, Park SY, on behalf of Korean Interstitial Lung Diseases Study Group

Idiopathic nonspecific interstitial pneumonia (NSIP) is one of the varieties of idiopathic interstitial pneumonias. Diagnosis of idiopathic NSIP can be done via multidisciplinary approach in which the clinical, radiologic, and...
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Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 1. Introduction

Park SW, Baek AR, Lee HL, Jeong SW, Yang SH, Kim YH, Chung MP, on behalf of the Korean Interstitial Lung Diseases Study Group

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...
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A Case of Desquamative Interstitial Pneumonia with an Increased Number of Eosinophils in Bronchoalveolar Lavage Fluid

Choi Y, Kim TH, Kang LH, Kim HJ, Jang JH, Shin DH, Jeon D

Here, we present a case of desquamative interstitial pneumonia (DIP) that was initially misdiagnosed as chronic eosinophilic pneumonia due to an increased number of eosinophils in the bronchoalveolar lavage fluid...
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Idiopathic Pleuroparenchymal Fibroelastosis Presenting in Recurrent Pneumothorax: A Case Report

Noh HJ, Seo Y, Huo SM, Kim TJ, Kim HL, Song JS

Idiopathic pleuroparenchymal fibroelastosis (PPFE) is a rare, recently classified entity that consists of pleural and subjacent parenchymal fibrosis predominantly in the upper lungs. In an official American Thoracic Society/European Respiratory...
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Clinical Significance of Serum Autoantibodies in Idiopathic Interstitial Pneumonia

Kang BH, Park JK, Roh JH, Song JW, Lee CK, Kim M, Jang SJ, Colby TV, Kim DS

Although autoantibodies are routinely screened in patients with idiopathic interstitial pneumonia, there are no reliable data on their clinical usefulness. The aim of this study was to investigate the prognostic...
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Radiologic Approach to the Idiopathic Interstitial Pneumonias

Oh YW

  • KMID: 2082452
  • Korean J Med.
  • 2013 Apr;84(4):489-497.
Idiopathic interstitial pneumonias (IIP), a heterogeneous group of diffuse parenchymal lung diseases, include seven clinicopathologic entities: idiopathic pulmonary fibrosis (IPF), nonspecific interstitial pneumonia (NSIP), cryptogenic organizing pneumonia (COP), acute interstitial...
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A Case of Bronchiolitis Interstitial Pneumonitis

Kim MJ, Kim YS, Kim DH, Jun TY, Lee SJ, Kim YJ

  • KMID: 2267916
  • Korean J Med.
  • 2013 Jan;84(1):105-110.
Interstitial lung diseases are diagnosed based on clinical, radiological, and histopathological findings. There are various kinds of interstitial lung diseases involving both the interstitium and bronchioles. Bronchiolitis interstitial pneumonitis (BIP)...
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Treatment Response and Long Term Follow-up Results of Nonspecific Interstitial Pneumonia

Lee JY, Jin SM, Lee BJ, Chung DH, Jang BG, Park HS, Lee SM, Yim JJ, Yang SC, Yoo CG, Han SK, Shim YS, Kim YW

The purpose of this study was to investigate the long-term clinical course of non-specific interstitial pneumonia (NSIP) and to determine which factors are associated with a response to steroid therapy...
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A Case of Asymptomatic, Localized, and Idiopathic Diffuse Alveolar Damage

Jeon YD, Hong HC, Joh JS, Jung JY, Min JW, Park SY, Lee GR

  • KMID: 2319812
  • Tuberc Respir Dis.
  • 2012 Apr;72(4):386-389.
Diffuse alveolar damage (DAD) is a histological change in lung tissue, and is generally caused by an acute lung injury, which is characterized by bilateral and widespread damages. Localized DAD...
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A Case Report of Usual Interstitial Pneumonia after Treatment of Bronchopneumonia

Lee JU, Shin SR, Kim HJ, Park JH

Usual interstitial pneumonia (UIP) is one type of idiopathic interstitial pneumonia, characterized by its poor prognosis and gradual deterioration of clinical course. So it is important to distinguish UIP from...
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2008 National Survey of Idiopathic Interstitial Pneumonia in Korea

Scientific Committee of the Korean Academy of Tuberculosis and Respiratory Diseases

  • KMID: 2319162
  • Tuberc Respir Dis.
  • 2009 Feb;66(2):141-151.
BACKGROUND: There is limited data on the epidemiology and relative frequency of idiopathic interstitial pneumonia (IIP) worldwide. This survey was performed to assess the epidemiology and relative frequency of IIP...
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Clinical Year in Review of Interstitial Lung Diseases: Focused on Idiopathic Interstitial Pneumonia

Lee WY

  • KMID: 2319248
  • Tuberc Respir Dis.
  • 2009 Oct;67(4):275-280.
Interstitial lung disease (ILD) is a group of diseases characterized by pulmonary interstitial inflammation. Finally the inflammation results in pulmonary fibrosis and impairment of oxygen transportation. The causes of idiopathic...
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Radiologic Diagnosis of Interstitial Lung Diseases

Yi CA, Lee KS

Diffuse interstitial lung diseases (DILD) are a group of chronic disorders showing varying degrees of active inflammation and established fibrosis mainly involving the interstitium of the lungs. DILD can be...
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Diagnostic Approaches to Diffuse Interstitial Lung Diseases

Kim DS

Diffuse interstitial lung diseases (DILDs) are a heterogeneous group of non-neoplastic, noninfectious disorders resulting from damage to the lung parenchyma, and present with similar clinical features. There has been difficulty...
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Clinical Features of the 15 Patients with Idiopathic Interstitial Pneumonia

Park SH, Ahn YH, Han JH, Kim JK, Ahn KM, Lee SI

  • KMID: 2314517
  • Pediatr Allergy Respir Dis.
  • 2007 Sep;17(3):271-281.
PURPOSE: Histologic classification plays a key role in the classification of idiopathic interstitial pneumonia (IIP) into clinically meaningful categories in terms of natural history, prognosis and treatment. The implications of...
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Cyclophosphamide in the Treatment of Idiopathic UIP and NSIP

Jeon K, Chung MP, Shin SC, Yu CM, Koh WJ, Suh GY, Kim H, Kwon OJ, Kim TS, Lee KS, Han J

BACKGROUND: Although corticosteroid and cytotoxic agent such as cyclophosphamide have been used for the treatment of idiopathic interstitial pneumonia (IIP), efficacy of these toxic drugs are unclear because previous reports...
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The Expression of Clara Cell Secretory Protein in BAL Fluid of Patients with Idiopathic Interstitial Pneumonia

Um SW, Han SJ, Choi CM, Lee CH, Yoo CG, Lee CT, Han SK, Shim YS, Kim YW

BACKGROUND: Idiopathic interstitial pneumonia is characterized by chronic inflammation and pulmonary fibrosis. The clara cell 10 kD protein (CC10, also designated CC16) is synthesized by the bronchial epithelium and...
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