Idiopathic interstitial pneumonia classification: Difference between revisions
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==Overview== | ==Overview== | ||
An idiopathic interstitial pneumonias (IIPs) classification faced difficulties as the disease behavior is overlapping, which makes it difficult to be classified from other pulmonary diseases of heterogenous clinical course.<ref name="www.atsjournals.org">{{Cite web | last = | first = | title = http://www.atsjournals.org/doi/abs/10.1164/rccm.201308-1483ST#.UoKrHChCCPE | url = http://www.atsjournals.org/doi/abs/10.1164/rccm.201308-1483ST#.UoKrHChCCPE | publisher = | date = | accessdate = 12 November 2013 }}</ref> . However the American Thoracic Society/European Respiratory Society (ATS/ERS) Classification of 2002 defined seven specific entities provided standardized terminology and diagnostic criteria.Later, many publications have led to adopt general changes in the 2007 statement update by ATS/ERS. The new changes emphasized that the histologic diagnosis as a historical gold standard is replaced by a multidisciplinary approach. With the era of molecular markers and multidisciplinary approach, surgical biopsy to diagnose the respiratory bronchiolitis-interstitial lung disease is not needed anymore, nonspecific interstitial pneumonia is now better defined and rare disease as pleuroparenchymal fibroelastosis is introduced. The heterogeneous mixed pattern with acute exacerbation is now defined as a clinical course for idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia. | An idiopathic interstitial pneumonias (IIPs) classification faced difficulties as the disease behavior is overlapping, which makes it difficult to be classified from other pulmonary diseases of heterogenous clinical course.<ref name="www.atsjournals.org">{{Cite web | last = | first = | title = http://www.atsjournals.org/doi/abs/10.1164/rccm.201308-1483ST#.UoKrHChCCPE | url = http://www.atsjournals.org/doi/abs/10.1164/rccm.201308-1483ST#.UoKrHChCCPE | publisher = | date = | accessdate = 12 November 2013 }}</ref> . However the American Thoracic Society/European Respiratory Society (ATS/ERS) Classification of 2002 defined seven specific entities provided standardized terminology and diagnostic criteria.Later, many publications have led to adopt general changes in the 2007 statement update by ATS/ERS. The new changes emphasized that the histologic diagnosis as a historical gold standard is replaced by a multidisciplinary approach with close interaction of clinician, radiologist, and pathologist. With the era of molecular markers and multidisciplinary approach, surgical biopsy to diagnose the respiratory bronchiolitis-interstitial lung disease is not needed anymore, nonspecific interstitial pneumonia is now better defined and rare disease as pleuroparenchymal fibroelastosis is introduced. The heterogeneous mixed pattern with acute exacerbation is now defined as a clinical course for [[idiopathic pulmonary fibrosis]] and [[nonspecific interstitial pneumonia]]. | ||
==2013 Revised ATS/ERC Classification of Idiopathic Interstitial Pneumonias: Multidisciplinary Diagnoses== | |||
===Major Idiopathic Interstitial Pneumonias=== | |||
== | |||
* [[Idiopathic pulmonary fibrosis]] | * [[Idiopathic pulmonary fibrosis]] | ||
* Idiopathic nonspecific interstitial pneumonia | * [[Idiopathic nonspecific interstitial pneumonia]] | ||
* [[Respiratory bronchiolitis-interstitial lung disease]] | * [[Respiratory bronchiolitis-interstitial lung disease]] | ||
* [[Desquamative interstitial pneumonia]] | * [[Desquamative interstitial pneumonia]] | ||
* [[Cryptogenic organizing pneumonia]] | * [[Cryptogenic organizing pneumonia]] | ||
* [[Acute interstitial pneumonia]] | * [[Acute interstitial pneumonia]] previously Hamman-Rich Syndrome. | ||
===Rare | ===Rare Idiopathic Interstitial Pneumonias=== | ||
* Idiopathic lymphoid interstitial pneumonia | * Idiopathic lymphoid interstitial pneumonia | ||
* Idiopathic pleuroparenchymal fibroelastosis | * Idiopathic pleuroparenchymal fibroelastosis | ||
===Unclassifiable | ===Unclassifiable Idiopathic Interstitial Pneumonias=== | ||
* Inadequate clinical, radiologic, or pathologic data | * Inadequate clinical, radiologic, or pathologic data | ||
* Major discordance between clinical, radiologic, and pathologic findings that may occur in the following situations | * Major discordance between clinical, radiologic, and pathologic findings that may occur in the following situations | ||
Latest revision as of 23:23, 15 November 2013
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Idiopathic Interstitial Pneumonia Microchapters |
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Differentiating Idiopathic interstitial pneumonia from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Idiopathic interstitial pneumonia classification On the Web |
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American Roentgen Ray Society Images of Idiopathic interstitial pneumonia classification |
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Directions to Hospitals Treating Idiopathic interstitial pneumonia |
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Risk calculators and risk factors for Idiopathic interstitial pneumonia classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, M.D. [2]; Chetan Lokhande, M.B.B.S [3]
Overview
An idiopathic interstitial pneumonias (IIPs) classification faced difficulties as the disease behavior is overlapping, which makes it difficult to be classified from other pulmonary diseases of heterogenous clinical course.[1] . However the American Thoracic Society/European Respiratory Society (ATS/ERS) Classification of 2002 defined seven specific entities provided standardized terminology and diagnostic criteria.Later, many publications have led to adopt general changes in the 2007 statement update by ATS/ERS. The new changes emphasized that the histologic diagnosis as a historical gold standard is replaced by a multidisciplinary approach with close interaction of clinician, radiologist, and pathologist. With the era of molecular markers and multidisciplinary approach, surgical biopsy to diagnose the respiratory bronchiolitis-interstitial lung disease is not needed anymore, nonspecific interstitial pneumonia is now better defined and rare disease as pleuroparenchymal fibroelastosis is introduced. The heterogeneous mixed pattern with acute exacerbation is now defined as a clinical course for idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia.
2013 Revised ATS/ERC Classification of Idiopathic Interstitial Pneumonias: Multidisciplinary Diagnoses
Major Idiopathic Interstitial Pneumonias
- Idiopathic pulmonary fibrosis
- Idiopathic nonspecific interstitial pneumonia
- Respiratory bronchiolitis-interstitial lung disease
- Desquamative interstitial pneumonia
- Cryptogenic organizing pneumonia
- Acute interstitial pneumonia previously Hamman-Rich Syndrome.
Rare Idiopathic Interstitial Pneumonias
- Idiopathic lymphoid interstitial pneumonia
- Idiopathic pleuroparenchymal fibroelastosis
Unclassifiable Idiopathic Interstitial Pneumonias
- Inadequate clinical, radiologic, or pathologic data
- Major discordance between clinical, radiologic, and pathologic findings that may occur in the following situations
- Previous therapy resulting in substantial alteration of radiologic or histologic findings (e.g., biopsy of desquamative interstitial pneumonia after steroid therapy, which shows only residual nonspecific interstitial pneumonia.
- New entity, or unusual variant of recognized entity, not adequately characterized by the current American Thoracic Society/European Respiratory Society classification (e.g., variant of organizing pneumonia with supervening fibrosis).
- Multiple high-resolution computed tomography and/or pathologic patterns that may be encountered in patients with idiopathic interstitial pneumonia.[2]
References
- ↑ "http://www.atsjournals.org/doi/abs/10.1164/rccm.201308-1483ST#.UoKrHChCCPE". Retrieved 12 November 2013. External link in
|title=(help) - ↑ Travis, WD.; Costabel, U.; Hansell, DM.; King, TE.; Lynch, DA.; Nicholson, AG.; Ryerson, CJ.; Ryu, JH.; Selman, M. (2013). "An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias". Am J Respir Crit Care Med. 188 (6): 733–48. doi:10.1164/rccm.201308-1483ST. PMID 24032382. Unknown parameter
|month=ignored (help)