Paroxysmal nocturnal hemoglobinuria classification: Difference between revisions

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{{Paroxysmal nocturnal hemoglobinuria}}
{{Paroxysmal nocturnal hemoglobinuria}}


{{CMG}}; {{AE}}  
{{CMG}}; {{AE}} {{AEL}}
 
==Overview==
==Overview==
There is no established system for the classification of [disease name].
Paroxysmal nocturnal hemoglobinuria may be classified according to the diagnosis results into three subtypes. The subtypes of PNH include classic PNH, secondary PNH, or subclinical PNH.  
 
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==


Paroxysmal nocturnal hemoglobinuria may be classified according to diagnosis results into three subtypes:
Paroxysmal nocturnal hemoglobinuria may be classified according to diagnosis results into three subtypes:<ref name="pmid1895106">{{cite journal| author=Mok WM, Herschkowitz S, Krieger NR| title=In vivo studies identify 5 alpha-pregnan-3 alpha-ol-20-one as an active anesthetic agent. | journal=J Neurochem | year= 1991 | volume= 57 | issue= 4 | pages= 1296-301 | pmid=1895106  | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1895106  }}</ref><ref name="pmid16051736">{{cite journal| author=Parker C, Omine M, Richards S, Nishimura J, Bessler M, Ware R et al.| title=Diagnosis and management of paroxysmal nocturnal hemoglobinuria. | journal=Blood | year= 2005 | volume= 106 | issue= 12 | pages= 3699-709 | pmid=16051736 | doi=10.1182/blood-2005-04-1717 | pmc=1895106 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16051736  }}</ref>
* Classic PNH: Other bone marrow disorders with a confirmed diagnosis of PNH.  
* Classic PNH: Other [[bone marrow]] disorders with a confirmed diagnosis of PNH.  
* Secondary PNH: When PNH is due to other bone marrow disorder as aplastic anemia or myelodysplastic syndrome.  
* Secondary PNH: When PNH is due to other bone marrow disorder as [[aplastic anemia]] or [[myelodysplastic syndrome]].  
* Subclinical PNH: No signs or symptoms of PNH, however, flow cytometry shows results of PNH.
* Subclinical PNH: No signs or symptoms of PNH, however, [[flow cytometry]] shows results of PNH.


==References==
==References==

Latest revision as of 23:02, 31 October 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]

Overview

Paroxysmal nocturnal hemoglobinuria may be classified according to the diagnosis results into three subtypes. The subtypes of PNH include classic PNH, secondary PNH, or subclinical PNH.

Classification

Paroxysmal nocturnal hemoglobinuria may be classified according to diagnosis results into three subtypes:[1][2]

References

  1. Mok WM, Herschkowitz S, Krieger NR (1991). "In vivo studies identify 5 alpha-pregnan-3 alpha-ol-20-one as an active anesthetic agent". J Neurochem. 57 (4): 1296–301. PMID 1895106  Check |pmid= value (help).
  2. Parker C, Omine M, Richards S, Nishimura J, Bessler M, Ware R; et al. (2005). "Diagnosis and management of paroxysmal nocturnal hemoglobinuria". Blood. 106 (12): 3699–709. doi:10.1182/blood-2005-04-1717. PMC 1895106. PMID 16051736.

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