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About 27,390 results

ALLMedicine™ Vasculitis Center

Research & Reviews  13,257 results

COVID-19-associated vasculitis and thrombotic complications: from pathological findings...
https://doi.org/10.1093/rheumatology/keaa581
Rheumatology (Oxford, England); Vacchi C, Meschiari M et. al.

Sep 24th, 2020 - COVID-19-associated vasculitis and thrombotic complications: from pathological findings to multidisciplinary discussion.|2020|Vacchi C,Meschiari M,Milic J,Marietta M,Tonelli R,|

Annular leukocytoclastic vasculitis in a patient with PR3-antineutrophil cytoplasmic an...
https://doi.org/10.1684/ejd.2020.3816
European Journal of Dermatology : EJD; Gambichler T, Susok L et. al.

Sep 24th, 2020 - Annular leukocytoclastic vasculitis in a patient with PR3-antineutrophil cytoplasmic antibody-positive ulcerative colitis.|2020|Gambichler T,Susok L,Abu Rached N,Stücker M,Scheel C,|

Clinical and pathological characteristics of ANA/anti-dsDNA positive patients with anti...
https://doi.org/10.1007/s00296-020-04704-3
Rheumatology International; Zhao X, Wen Q et. al.

Sep 23rd, 2020 - Antineutrophil cytoplasmic autoantibodies (ANCA) associated vasculitis (AAV) consists of a group of systemic autoimmune diseases. The roles of serum anti-nuclear antibodies (ANA) and anti-double-stranded DNA (anti-dsDNA) antibodies in AAV patients...

Mepolizumab as a steroid-sparing agent in eosinophilic granulomatosis with polyangiitis...
https://doi.org/10.1080/02770903.2020.1827417
The Journal of Asthma : Official Journal of the Association for the Care of Asthma; Vergles M, Matković Z et. al.

Sep 23rd, 2020 - Introduction: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of small-vessel vasculitis characterized by asthma, hyper-eosinophilia, and progressive multiorgan involvement. EGPA is traditionally treated using corticosteroids, ...

PEXIVAS: The End of Plasmapheresis for ANCA-Associated Vasculitis?
https://doi.org/10.2215/CJN.10550620
Clinical Journal of the American Society of Nephrology : CJASN; De Vriese AS, Fervenza FC

Sep 23rd, 2020 - PEXIVAS: The End of Plasmapheresis for ANCA-Associated Vasculitis?|2020|De Vriese AS,Fervenza FC,|

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Guidelines  27 results

European consensus-based recommendations for diagnosis and treatment of immunoglobulin ...
https://doi.org/10.1093/rheumatology/kez041
Rheumatology (Oxford, England); Ozen S, Marks SD et. al.

Mar 17th, 2019 - IgA vasculitis (IgAV, formerly known as Henoch-Schönlein purpura) is the most common cause of systemic vasculitis in childhood. To date, there are no internationally agreed, evidence-based guidelines concerning the appropriate diagnosis and treatm...

Outline of guidelines for the management of vasculitis and vascular disorders in Japan,...
https://doi.org/10.1111/1346-8138.14086
The Journal of Dermatology; Ikeda T, Furukawa F et. al.

Oct 6th, 2017 - The proposal by the 1994 International Chapel Hill Consensus Conference on the Nomenclature of Systemic Vasculitides (CHCC1994) and by the CHCC2012 markedly influenced the classification and way of considering cutaneous vasculitis. In the proposal...

Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statem...
https://doi.org/10.1161/CIR.0000000000000484
Circulation McCrindle BW, Rowley AH et. al.

Mar 30th, 2017 - Kawasaki disease is an acute vasculitis of childhood that leads to coronary artery aneurysms in ≈25% of untreated cases. It has been reported worldwide and is the leading cause of acquired heart disease in children in developed countries. To revis...

IgA vasculitis (Henoch-Schönlein): Case definition andguidelines for data collection, a...
https://doi.org/10.1016/j.vaccine.2016.09.024
Vaccine Woerner A, Rudin C et. al.

Dec 30th, 2016 - IgA vasculitis (Henoch-Schönlein): Case definition andguidelines for data collection, analysis, and presentation of immunisation safety data.|2016|Woerner A,Rudin C,Bonetto C,Santuccio C,Ozen S,|adverse effects,classification,diagnosis,immunology,...

EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis.
https://doi.org/10.1136/annrheumdis-2016-209133
Annals of the Rheumatic Diseases; Yates M, Watts RA et. al.

Jun 24th, 2016 - In this article, the 2009 European League Against Rheumatism (EULAR) recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) have been updated. The 2009 recommendations were on the management of...

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Drugs  1 results see all →

Clinicaltrials.gov  13,473 results

COVID-19-associated vasculitis and thrombotic complications: from pathological findings...
https://doi.org/10.1093/rheumatology/keaa581
Rheumatology (Oxford, England); Vacchi C, Meschiari M et. al.

Sep 24th, 2020 - COVID-19-associated vasculitis and thrombotic complications: from pathological findings to multidisciplinary discussion.|2020|Vacchi C,Meschiari M,Milic J,Marietta M,Tonelli R,|

Annular leukocytoclastic vasculitis in a patient with PR3-antineutrophil cytoplasmic an...
https://doi.org/10.1684/ejd.2020.3816
European Journal of Dermatology : EJD; Gambichler T, Susok L et. al.

Sep 24th, 2020 - Annular leukocytoclastic vasculitis in a patient with PR3-antineutrophil cytoplasmic antibody-positive ulcerative colitis.|2020|Gambichler T,Susok L,Abu Rached N,Stücker M,Scheel C,|

Clinical and pathological characteristics of ANA/anti-dsDNA positive patients with anti...
https://doi.org/10.1007/s00296-020-04704-3
Rheumatology International; Zhao X, Wen Q et. al.

Sep 23rd, 2020 - Antineutrophil cytoplasmic autoantibodies (ANCA) associated vasculitis (AAV) consists of a group of systemic autoimmune diseases. The roles of serum anti-nuclear antibodies (ANA) and anti-double-stranded DNA (anti-dsDNA) antibodies in AAV patients...

Mepolizumab as a steroid-sparing agent in eosinophilic granulomatosis with polyangiitis...
https://doi.org/10.1080/02770903.2020.1827417
The Journal of Asthma : Official Journal of the Association for the Care of Asthma; Vergles M, Matković Z et. al.

Sep 23rd, 2020 - Introduction: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of small-vessel vasculitis characterized by asthma, hyper-eosinophilia, and progressive multiorgan involvement. EGPA is traditionally treated using corticosteroids, ...

PEXIVAS: The End of Plasmapheresis for ANCA-Associated Vasculitis?
https://doi.org/10.2215/CJN.10550620
Clinical Journal of the American Society of Nephrology : CJASN; De Vriese AS, Fervenza FC

Sep 23rd, 2020 - PEXIVAS: The End of Plasmapheresis for ANCA-Associated Vasculitis?|2020|De Vriese AS,Fervenza FC,|

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News  579 results

Pediatric Dermatology Emergencies
https://www.mdedge.com/dermatology/article/218463/pediatrics/pediatric-dermatology-emergencies/page/0/3?channel=271

Mar 5th, 2020 - IgA Vasculitis Presentation IgA vasculitis, or Henoch-Schönlein purpura, classically presents as a tetrad of palpable purpura, acute-onset arthritis or arthralgia, abdominal pain, and renal disease with proteinuria or hematuria. 30 Skin involvement.

Novartis stands by safety of eye drug amid ongoing review
https://www.reuters.com/article/us-novartis-beovu/novartis-stands-by-safety-of-eye-drug-amid-ongoing-review-idUSKBN20P2AS

Mar 2nd, 2020 - FILE PHOTO: The company's logo is seen at a building of Swiss drugmaker Novartis in Rotkreuz, Switzerland, January 29, 2020. REUTERS/Arnd Wiegmann ZURICH (Reuters) - Swiss drugmaker Novartis said on Monday the safety data available for its eye dru...

Antineutrophil Cytoplasmic Antibody Vasculitis Induced by Hydralazine
https://www.mdedge.com/dermatology/article/217100/mixed-topics/antineutrophil-cytoplasmic-antibody-vasculitis-induced/page/0/2?channel=44

Feb 11th, 2020 - A comprehensive drug history from at least 6 months prior to presentation is essential. Biopsies also are strongly encouraged to confirm the presence of vasculitis and to determine its severity.

Hypersensitivity Reactions to Orthopedic Implants: What’s All the Hype?
https://www.mdedge.com/dermatology/article/216696/contact-dermatitis/hypersensitivity-reactions-orthopedic-implants-whats/page/0/1?channel=54

Feb 4th, 2020 - Clinical Presentation Several clinical presentations of orthopedic IHRs have been described. Perhaps the most commonly recognized is a localized cutaneous eczematous eruption, with dermatitis typically overlying the site of the implanted material.

Rash on legs and abdomen
https://www.mdedge.com/familymedicine/article/215177/dermatology/rash-legs-and-abdomen?channel=114
MDedge Family Medicine;

Jan 16th, 2020 - The rash was consistent with nonblanching purpura. Two punch biopsies were performed for hematoxylin and eosin stain and direct immunofluorescence, which were consistent with IgA mediated small vessel vasculitis, or Henoch-Schoenlein purpura.

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Patient Education  53 results see all →