SAT0346 Cutaneous Vasculitis Associated To Connective Tissue Diseases and Other Autoimmune Disorders. Study of 35 Patients from A Single Centre. (15th July 2016)
- Record Type:
- Journal Article
- Title:
- SAT0346 Cutaneous Vasculitis Associated To Connective Tissue Diseases and Other Autoimmune Disorders. Study of 35 Patients from A Single Centre. (15th July 2016)
- Main Title:
- SAT0346 Cutaneous Vasculitis Associated To Connective Tissue Diseases and Other Autoimmune Disorders. Study of 35 Patients from A Single Centre
- Authors:
- Fernández-Díaz, C.
Loricera, J.
Blanco, R.
Hernández, J.L.
Calvo-Río, V.
Ortiz-Sanjuán, F.
Fernández-Llaca, H.
González-Lόpez, M.A.
Armesto, S.
González-Vela, C.
González-Gay, M.Ά. - Abstract:
- Abstract : Background: Cutaneous vasculitis (CV) can be a clinical manifestation of a connective tissue or other autoimmune disease. Objectives: Our aim was to assess the frequency and clinical features of CV associated to connective tissue diseases. Methods: Study of a large series of 766 unselected patients with CV attended in the same tertiary-care hospital. CV was considered as secondary to connective tissue disease or other autoimmune disorder when occurred in the setting of any of these conditions. Results: In 35 (10 men/25 women; mean age±SD, 48±15 years) of 766 patients (4.57%) CV was associated to the following connective tissue disease or autoimmune disorder: systemic lupus erythematosus (SLE) (n=15), rheumatoid arthritis (n=9), Sjögren's syndrome (n=5), ankylosing spondylitis (n=2), relapsing polychondritis (n=1), Behçet's disease (n=1), sarcoidosis (n=1) and autoimmune hepatitis (n=1). All patients developed vasculitic skin lesions: palpable purpura (n=31), maculopapular erythema (n=4) and urticarial lesions (n=2). The most common CV locations were: lower limbs (n=30), upper limbs (n=12) and trunk (n=10). The mean duration of skin lesions was 13.83±7.62 days. Other clinical features were nephropathy (n=9), joint involvement (n=6), constitutional symptoms (n=4) and gastrointestinal involvement (n=1). Regarding laboratory parameters, elevated ESR was observed in 25 patients, hematuria in 4, anemia in 7 and proteinuria in 5 patients. Immunologic findings were asAbstract : Background: Cutaneous vasculitis (CV) can be a clinical manifestation of a connective tissue or other autoimmune disease. Objectives: Our aim was to assess the frequency and clinical features of CV associated to connective tissue diseases. Methods: Study of a large series of 766 unselected patients with CV attended in the same tertiary-care hospital. CV was considered as secondary to connective tissue disease or other autoimmune disorder when occurred in the setting of any of these conditions. Results: In 35 (10 men/25 women; mean age±SD, 48±15 years) of 766 patients (4.57%) CV was associated to the following connective tissue disease or autoimmune disorder: systemic lupus erythematosus (SLE) (n=15), rheumatoid arthritis (n=9), Sjögren's syndrome (n=5), ankylosing spondylitis (n=2), relapsing polychondritis (n=1), Behçet's disease (n=1), sarcoidosis (n=1) and autoimmune hepatitis (n=1). All patients developed vasculitic skin lesions: palpable purpura (n=31), maculopapular erythema (n=4) and urticarial lesions (n=2). The most common CV locations were: lower limbs (n=30), upper limbs (n=12) and trunk (n=10). The mean duration of skin lesions was 13.83±7.62 days. Other clinical features were nephropathy (n=9), joint involvement (n=6), constitutional symptoms (n=4) and gastrointestinal involvement (n=1). Regarding laboratory parameters, elevated ESR was observed in 25 patients, hematuria in 4, anemia in 7 and proteinuria in 5 patients. Immunologic findings were as follows: positive rheumatoid factor (10 of 13 patients tested), positive antinuclear antibodies (15 of 19 patients tested), and decreased serum complement levels (11 of 20 patients tested). Twenty-five patients required some drug for CV: corticosteroids (n=22), cyclophosphamide (n=6), methotrexate (n=5), NSAIDs (n=4), azathioprine (n=4), chloroquine (n=3), hidroxichloroquine (n=2), dapsone (n=1) and rituximab (n=2). Conclusions: CV, although infrequent, is not exceptional in the setting of any connective tissue disease or autoimmune disorder. Acknowledgement: This study was supported by a grant from "Fondo de Investigaciones Sanitarias" PI12/00193 (Spain). This work was also partially supported by RETICS Programs, RD08/0075 (RIER) and RD12/0009/0013 from "Instituto de Salud Carlos III" (ISCIII) (Spain). Disclosure of Interest: None declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 75(2016)Supplement 2
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 75(2016)Supplement 2
- Issue Display:
- Volume 75, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 75
- Issue:
- 2
- Issue Sort Value:
- 2016-0075-0002-0000
- Page Start:
- 792
- Page End:
- 792
- Publication Date:
- 2016-07-15
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2016-eular.5259 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17926.xml