Differentiating systemic lupus erythematosus from other diseases: Difference between revisions
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! align="center" style="background:#4479BA; color: #FFFFFF;" |Anti-dsDNA | ! align="center" style="background:#4479BA; color: #FFFFFF;" |Anti-dsDNA | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |[[Systemic lupus erythematosus]] | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |[[Rheumatoid arthritis]] ([[Rheumatoid arthritis|RA]]) | ||
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* | * | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Rhupus | ||
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|Erosive [[arthropathy]] | |||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |[[Mixed connective tissue disease]] (MCTD)<ref name="pmid21959290">{{cite journal |vauthors=Cappelli S, Bellando Randone S, Martinović D, Tamas MM, Pasalić K, Allanore Y, Mosca M, Talarico R, Opris D, Kiss CG, Tausche AK, Cardarelli S, Riccieri V, Koneva O, Cuomo G, Becker MO, Sulli A, Guiducci S, Radić M, Bombardieri S, Aringer M, Cozzi F, Valesini G, Ananyeva L, Valentini G, Riemekasten G, Cutolo M, Ionescu R, Czirják L, Damjanov N, Rednic S, Matucci Cerinic M |title="To be or not to be," ten years after: evidence for mixed connective tissue disease as a distinct entity |journal=Semin. Arthritis Rheum. |volume=41 |issue=4 |pages=589–98 |year=2012 |pmid=21959290 |doi=10.1016/j.semarthrit.2011.07.010 |url=}}</ref> | ||
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|Overlapping features of SLE, [[systemic sclerosis]] (SSc), and [[polymyositis]] (PM) | |||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |[[Undifferentiated connective tissue disease]] (UCTD) | ||
| + | | + | ||
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| | |Lower extremity | ||
|↑ | |↑ | ||
|↑ | |↑ | ||
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| + | | + | ||
|erythematous macules, patches, or papules with delicate scale | |||
mostly in lower extremities | |||
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* | * | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |[[Systemic sclerosis]] (SSc) | ||
|<nowiki>+/-</nowiki> | |<nowiki>+/-</nowiki> | ||
|<nowiki>+</nowiki> | |<nowiki>+</nowiki> | ||
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|↑ | |↑ | ||
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| | |skin thickening and hardening and edematous swelling and erythema | ||
|[[Sclerodactyly]], [[Telangiectasias]], [[Calcinosis]], [[Malignant hypertension]], [[acute renal failure]] | |||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Sjögren’s syndrome | ||
15485020 | 15485020 | ||
|<nowiki>+/-</nowiki> | |<nowiki>+/-</nowiki> | ||
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| | |xerosis, scaly skin, annular erythema | ||
| | |[[Keratoconjunctivitis sicca]], [[Xerostomia]] | ||
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| rowspan="3" | | rowspan="3" align="center" style="background:#DCDCDC;" |Vasculitis | ||
| align="center" style="background:#DCDCDC;" |Giant cell | | align="center" style="background:#DCDCDC;" |Giant cell | ||
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| rowspan="3"| | | rowspan="3" | | ||
| | |Rare | ||
|Involvement of ranial branches of arteries, visual loss | |||
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| align="center" style="background:#DCDCDC;" |[[Takayasu's arteritis|Takayasu]] | | align="center" style="background:#DCDCDC;" |[[Takayasu's arteritis|Takayasu]] | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Behçet’s syndrome | ||
|<nowiki>+/-</nowiki> | |<nowiki>+/-</nowiki> | ||
|<nowiki>+/-</nowiki> | |<nowiki>+/-</nowiki> | ||
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* [[ANA]]-negative | * [[ANA]]-negative | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Kikuchi’s disease | ||
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|<nowiki>+/-</nowiki> | |<nowiki>+/-</nowiki> | ||
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* May be associated with SLE | * May be associated with SLE | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Serum sickness | ||
|<nowiki>+/-</nowiki> | |<nowiki>+/-</nowiki> | ||
|<nowiki>+</nowiki> | |<nowiki>+</nowiki> | ||
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* Self-limited | * Self-limited | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Psoriatic arthritis | ||
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| colspan="2" | | colspan="2" align="center" style="background:#DCDCDC;" |Human [[parvovirus]] B19 infection | ||
|<nowiki>+</nowiki> | |<nowiki>+</nowiki> | ||
|<nowiki>+</nowiki> | |<nowiki>+</nowiki> |
Revision as of 19:34, 11 July 2017
Systemic lupus erythematosus Microchapters |
Differentiating Systemic lupus erythematosus from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mahshid Mir, M.D. [2]
Overview
Systemic lupus erythematosus (SLE) must be differentiated from other diseases that cause skin rash, arthritis, positive autoimmune serology, weight loss, fevers and chronic pain, such as rheumatoid arthritis(RA), mixed connective tissue disease (MCTD), systemic sclerosis (SSc), dermatomyositis (DM), polymyositis(PM), and other autoimmune diseases.
Differentiating systemic lupus erythematosus from other diseases
Systemic lupus erythematosus (SLE) must be differentiated from other diseases that cause skin rash, arthritis, positive autoimmune serology, weight loss, fevers and chronic pain, such as rheumatoid arthritis(RA), mixed connective tissue disease (MCTD), systemic sclerosis (SSc), dermatomyositis (DM), polymyositis(PM), and other autoimmune diseases.
Differetiating SLE from other diseases that cause arthritis and rash
n | Arthritis | Auto-antibodies | Raynaud phenamon | Rash pattern | Distinguishing/specific features | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Polyarthritis | Tenderness | Edema | Deformity /Erosion | Pattern | ANA | RF | Anti-CCp | anti U1RNP | AntiSm | AntiRo | Anti-dsDNA | |||||
Systemic lupus erythematosus | Small joints | |||||||||||||||
Rheumatoid arthritis (RA) | + | + | + | + | Small and large joints | ↑↑ | ↑↑ | + |
| |||||||
Rhupus | + | + | + | + | Small and large joints | ↑ | ↑ | ↑ | ↑ | ↑ | ↑ | + | Erosive arthropathy | |||
Mixed connective tissue disease (MCTD)[1] | + | Small and large joints | ↑↑ | ↑ | + | Overlapping features of SLE, systemic sclerosis (SSc), and polymyositis (PM) | ||||||||||
Undifferentiated connective tissue disease (UCTD) | + | Lower extremity | ↑ | ↑ | ↑ | + | erythematous macules, patches, or papules with delicate scale
mostly in lower extremities |
| ||||||||
Systemic sclerosis (SSc) | +/- | + | + | +/- | ↑↑ | ↑ | ↑ | + | skin thickening and hardening and edematous swelling and erythema | Sclerodactyly, Telangiectasias, Calcinosis, Malignant hypertension, acute renal failure | ||||||
Sjögren’s syndrome
15485020 |
+/- | +/- | Lower extremity
and axiallary creases |
↑ | ↑ | xerosis, scaly skin, annular erythema | Keratoconjunctivitis sicca, Xerostomia | |||||||||
Vasculitis | Giant cell | + | + | Rare | Involvement of ranial branches of arteries, visual loss | |||||||||||
Takayasu | +/- | +/- |
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Poly-arteritis nodosa | +/- |
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Behçet’s syndrome | +/- | +/- | +/- |
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Kikuchi’s disease | +/- | ↑/↓ |
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Serum sickness | +/- | + | +/- |
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Psoriatic arthritis | Small and large joints | |||||||||||||||
Human parvovirus B19 infection | + | + | Small joints |
|
|
References
- ↑ Cappelli S, Bellando Randone S, Martinović D, Tamas MM, Pasalić K, Allanore Y, Mosca M, Talarico R, Opris D, Kiss CG, Tausche AK, Cardarelli S, Riccieri V, Koneva O, Cuomo G, Becker MO, Sulli A, Guiducci S, Radić M, Bombardieri S, Aringer M, Cozzi F, Valesini G, Ananyeva L, Valentini G, Riemekasten G, Cutolo M, Ionescu R, Czirják L, Damjanov N, Rednic S, Matucci Cerinic M (2012). ""To be or not to be," ten years after: evidence for mixed connective tissue disease as a distinct entity". Semin. Arthritis Rheum. 41 (4): 589–98. doi:10.1016/j.semarthrit.2011.07.010. PMID 21959290.