Scleroderma classification: Difference between revisions
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*Scleroderma (systemic sclerosis) is now classified according to the new American College of Rheumatology (ACR)/ European League Against Rheumatism (EULAR): | *Scleroderma (systemic sclerosis) is now classified according to the new American College of Rheumatology (ACR)/ European League Against Rheumatism (EULAR): | ||
{| class="wikitable" | |||
!Item | |||
!Sub-item(s) | |||
!Weight/Score | |||
|- | |||
|Skin thickening of the fingers of both hands extending proximal to the metacarpophalangeal joints (sufficient criterion) | |||
| - | |||
|9 | |||
|- | |||
|Skin thickening of the fingers (only count higher score) | |||
|Puffy fingers | |||
Sclerodactyly of the fingers (distal to the metacarpophalangeal joints but proximal to the proximal interphalangeal joints) | |||
|2 | |||
4 | |||
|- | |||
|Fingertip lesions (only count the higher score) | |||
|Digital tip ulcers | |||
Fingertip pitting scars | |||
|2 | |||
3 | |||
|- | |||
|Telangiectasia | |||
| - | |||
|2 | |||
|- | |||
|Abnormal nail fold capillaries | |||
| - | |||
|2 | |||
|- | |||
|Pulmonary arterial hypertension and/or Interstitial lung disease | |||
| | |||
|2 | |||
|- | |||
|Raynaud's phenomenon (RP) | |||
| - | |||
|3 | |||
|- | |||
|Any of the Scleroderma related autoantibodies | |||
|Anticentromere | |||
Anti-topoisomerase I (anti-SCL-70) | |||
Anti-RNA polymerase-3 | |||
|3 | |||
|} | |||
==References== | ==References== |
Revision as of 19:59, 27 March 2018
Scleroderma Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: M. Khurram Afzal, 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
- Scleroderma was previously classified according to American College of Rheumatology (ACR) 1980 preliminary scleroderma criteria:
- Major criteria:
- Proximal cutaneous sclerosis (skin thickening-nonpitting) of fingers that also extended proximally to the metacarpophalangeal joints (MCPs)
- Minor criteria:
- Sclerodactyly
- Digital pitting scars of fingertips or loss of substance of the distal finger pad (digital tuft resorption)
- Bibasilar pulmonary fibrosis
- Major criteria:
- If major criteria was present that was sufficient otherwise 2 of 3 minor criteria had to be present.
- Scleroderma (systemic sclerosis) is now classified according to the new American College of Rheumatology (ACR)/ European League Against Rheumatism (EULAR):
Item | Sub-item(s) | Weight/Score |
---|---|---|
Skin thickening of the fingers of both hands extending proximal to the metacarpophalangeal joints (sufficient criterion) | - | 9 |
Skin thickening of the fingers (only count higher score) | Puffy fingers
Sclerodactyly of the fingers (distal to the metacarpophalangeal joints but proximal to the proximal interphalangeal joints) |
2
4 |
Fingertip lesions (only count the higher score) | Digital tip ulcers
Fingertip pitting scars |
2
3 |
Telangiectasia | - | 2 |
Abnormal nail fold capillaries | - | 2 |
Pulmonary arterial hypertension and/or Interstitial lung disease | 2 | |
Raynaud's phenomenon (RP) | - | 3 |
Any of the Scleroderma related autoantibodies | Anticentromere
Anti-topoisomerase I (anti-SCL-70) Anti-RNA polymerase-3 |
3 |