Hamman-Rich syndrome classification: Difference between revisions
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==Classification== | ==Classification== | ||
*According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, Acute interstitial pneumonitis is a variant of a group of Idiopathic interstitial lung diseases.<ref name="pmid11790668">{{cite journal |vauthors= |title=American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001 |journal=Am. J. Respir. Crit. Care Med. |volume=165 |issue=2 |pages=277–304 |date=January 2002 |pmid=11790668 |doi=10.1164/ajrccm.165.2.ats01 |url=}}</ref> | *According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, [[Hamman-Rich syndrome|Acute interstitial pneumonitis]] is a variant of a group of Idiopathic interstitial lung diseases.<ref name="pmid11790668">{{cite journal |vauthors= |title=American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001 |journal=Am. J. Respir. Crit. Care Med. |volume=165 |issue=2 |pages=277–304 |date=January 2002 |pmid=11790668 |doi=10.1164/ajrccm.165.2.ats01 |url=}}</ref> | ||
*This classification divides Idiopathic interstitial pneumonias into 7 clinicopathological entities. | *This classification divides Idiopathic interstitial pneumonias into 7 clinicopathological entities. | ||
**Idiopathic pulmonary fibrosis (IPF) | **[[Idiopathic pulmonary fibrosis]] (IPF) | ||
**Nonspecific interstitial pneumonia (NSIP) | **[[Nonspecific interstitial pneumonia]] (NSIP) | ||
**Respiratory bronchiolitis-associated interstitial lung disease | **[[Respiratory bronchiolitis-interstitial lung disease|Respiratory bronchiolitis-associated interstitial lung disease]] | ||
**Respiratory bronchiolitis-associated lung disease/desquamative interstitial pneumonia | **[[Desquamative interstitial pneumonia|Respiratory bronchiolitis-associated lung disease/desquamative interstitial pneumonia]] | ||
**Cryptogenic organizing pneumonia | **[[Cryptogenic organizing pneumonia]] | ||
**Acute interstitial pneumonia | **[[Hamman-Rich syndrome|Acute interstitial pneumonia]] | ||
** | **[[Lymphocytic interstitial pneumonia]] (LIP) | ||
Revision as of 20:55, 21 March 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Chandrakala Yannam, MD [2]
Overview
There is no established system for the classification of [disease name].
OR
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].
OR
[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3]. [Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].
OR
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
OR
If the staging system involves specific and characteristic findings and features: According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
OR
The staging of [malignancy name] is based on the [staging system].
OR
There is no established system for the staging of [malignancy name].
Classification
- According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, Acute interstitial pneumonitis is a variant of a group of Idiopathic interstitial lung diseases.[1]
- This classification divides Idiopathic interstitial pneumonias into 7 clinicopathological entities.
- Idiopathic pulmonary fibrosis (IPF)
- Nonspecific interstitial pneumonia (NSIP)
- Respiratory bronchiolitis-associated interstitial lung disease
- Respiratory bronchiolitis-associated lung disease/desquamative interstitial pneumonia
- Cryptogenic organizing pneumonia
- Acute interstitial pneumonia
- Lymphocytic interstitial pneumonia (LIP)
References
- ↑ "American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001". Am. J. Respir. Crit. Care Med. 165 (2): 277–304. January 2002. doi:10.1164/ajrccm.165.2.ats01. PMID 11790668.