Hamman-Rich syndrome classification: Difference between revisions

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==Overview==
==Overview==
There is no established system for the classification of [disease name].
According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, [[Hamman-Rich syndrome|Acute interstitial pneumonitis]] is an entity of a group of Idiopathic interstitial lung diseases. The classification is based on [[clinical]], [[Radiology|radiological]] and [[Histopathology|histopathologic]] findings. The [[classification]] has been updated by ATS/ERS International multidisciplinary panel recently based on the [[literature review]] on idiopathic interstitial lung diseases published between 2000-2011.
 
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==
==Classification==
 
*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><ref name="pmid16304241">{{cite journal |vauthors=Leslie KO |title=Historical perspective: a pathologic approach to the classification of idiopathic interstitial pneumonias |journal=Chest |volume=128 |issue=5 Suppl 1 |pages=513S–519S |date=November 2005 |pmid=16304241 |doi=10.1378/chest.128.5_suppl_1.513S |url=}}</ref>
*There is no established system for the classification of [disease name].
*This classification divides Idiopathic interstitial pneumonias into 7 clinicopathological entities.
OR
**[[Idiopathic pulmonary fibrosis]] (IPF)
*[Disease name] may be classified according to [classification method] into [number] subtypes/groups:
**[[Nonspecific interstitial pneumonia]] (NSIP)
**[Group1]
**[[Respiratory bronchiolitis-interstitial lung disease|Respiratory bronchiolitis-associated interstitial lung disease]]
**[Group2]
**[[Desquamative interstitial pneumonia|Respiratory bronchiolitis-associated lung disease/desquamative interstitial pneumonia]]
**[Group3]
**[[Cryptogenic organizing pneumonia]]
**[Group4]
**[[Hamman-Rich syndrome|Acute interstitial pneumonia]]
OR
**[[Lymphocytic interstitial pneumonia]] (LIP)
*[Disease name] may be classified into [large number > 6] subtypes based on:
*American Thoracic Society/European Respiratory Society (ATS/ERS) panel [[classification]] of Idiopathic [[Interstitial lung disease|interstitial lung diseases]] has been updated recently,including changes to previously described clinical entities, describing new clinical entities, and describing new [[Histology|histologic patterns]] using [[literature review]] between 2000-2011.<ref name="pmid24032382">{{cite journal |vauthors=Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D |title=An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias |journal=Am. J. Respir. Crit. Care Med. |volume=188 |issue=6 |pages=733–48 |date=September 2013 |pmid=24032382 |pmc=5803655 |doi=10.1164/rccm.201308-1483ST |url=}}</ref>
**[Classification method 1]
*Revised classification of American thoracic society/European respiratory society international multidisciplinary panel of [[Idiopathic interstitial pneumonia|Idiopathic interstitial pneumonias]]:
**[Classification method 2]
**Major idiopathic interstitial pneumonias
**[Classification method 3]
***[[Idiopathic pulmonary fibrosis]]
*[Disease name] may be classified into several subtypes based on:  
***Idiopathic nonspecific interstitial pneumonia
**[Classification method 1]
***Respiratory bronchiolitis–interstitial lung disease
**[Classification method 2]
***[[Desquamative interstitial pneumonia]]
**[Classification method 3]
***[[Cryptogenic organizing pneumonia]]
OR
***[[Hamman-Rich syndrome|Acute interstitial pneumonia]]
*Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
**Rare idiopathic interstitial pneumonias
OR
***[[Lymphoid interstitial pneumonia|Idiopathic lymphoid interstitial pneumonia]]
*If the staging system involves specific and characteristic findings and features:
***Idiopathic pleuroparenchymal fibroelastosis
*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].
**Unclassifiable idiopathic interstitial pneumonia
OR
*The staging of [malignancy name] is based on the [staging system].
OR
*There is no established system for the staging of [malignancy name].
 
 
 




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[[Category:Pulmonology]]
[[Category: Pulmonology]]

Latest revision as of 20:56, 23 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

According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, Acute interstitial pneumonitis is an entity of a group of Idiopathic interstitial lung diseases. The classification is based on clinical, radiological and histopathologic findings. The classification has been updated by ATS/ERS International multidisciplinary panel recently based on the literature review on idiopathic interstitial lung diseases published between 2000-2011.

Classification


References

  1. ↑ "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.
  2. ↑ Leslie KO (November 2005). "Historical perspective: a pathologic approach to the classification of idiopathic interstitial pneumonias". Chest. 128 (5 Suppl 1): 513S–519S. doi:10.1378/chest.128.5_suppl_1.513S. PMID 16304241.
  3. ↑ Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D (September 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. PMC 5803655. PMID 24032382.

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