Adult-onset Still's disease classification: Difference between revisions

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==Classification==
==Classification==
=== Classification based on clinical presentation ===
Adult-onset Stiil's disease (AOSD) may be classified based on the predominant clinical picture with which the patient presents. The following are the sub-types:<ref name="pmid15642140">{{cite journal |vauthors=Villanueva J, Lee S, Giannini EH, Graham TB, Passo MH, Filipovich A, Grom AA |title=Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome |journal=Arthritis Res. Ther. |volume=7 |issue=1 |pages=R30–7 |date=2005 |pmid=15642140 |pmc=1064882 |doi=10.1186/ar1453 |url=}}</ref>
* ASOD with pre-dominant systemic symptoms
* ASOD with pre-dominant arthritis
{| class="wikitable"
! rowspan="5" |Adult-onset Still's disease sub-types
! rowspan="3" |Systemic sub-type
! colspan="5" |Distinguishing features
|-
!Pre-dominant cellular mechanism
!Clinical presentation
!Cytokine profile
!Response to treatment
!Miscellaneous
|-
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* Natural killer (NK) cell dysfunction (deficiency)
* CD8 type (cytotoxic) T cell dysfunction (deficiency)
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! rowspan="2" |Arthritis sub-type
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|}


==References==
==References==
{{reflist|2}}
{{reflist|2}}

Revision as of 23:13, 7 April 2018


Template:Adult-onset Still's disease Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Classification

Classification based on clinical presentation

Adult-onset Stiil's disease (AOSD) may be classified based on the predominant clinical picture with which the patient presents. The following are the sub-types:[1]

  • ASOD with pre-dominant systemic symptoms
  • ASOD with pre-dominant arthritis
Adult-onset Still's disease sub-types Systemic sub-type Distinguishing features
Pre-dominant cellular mechanism Clinical presentation Cytokine profile Response to treatment Miscellaneous
  • Natural killer (NK) cell dysfunction (deficiency)
  • CD8 type (cytotoxic) T cell dysfunction (deficiency)
Arthritis sub-type

References

  1. Villanueva J, Lee S, Giannini EH, Graham TB, Passo MH, Filipovich A, Grom AA (2005). "Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome". Arthritis Res. Ther. 7 (1): R30–7. doi:10.1186/ar1453. PMC 1064882. PMID 15642140.