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4101 search results for:

IgA Vasculitis 

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  1. Open Access 01-12-2024 | Biomarkers | OriginalPaper

    Deregulation in adult IgA vasculitis skin as the basis for the discovery of novel serum biomarkers

    Immunoglobulin A vasculitis (IgAV) is an immune complex leukocytoclastic vasculitis characterized by the dominant deposition of immunoglobulin (Ig) A in the affected vascular wall [ 1 ]. Cutaneous vasculitis in a form of palpable purpura represents …

  2. Open Access 01-12-2024 | IgA Vasculitis | OriginalPaper

    Characteristics of renal pathology and coagulation function in IgA nephropathy and IgA vasculitis associated nephritis

    IgAN is the most common primary glomerulonephritis worldwide and mainly affects the young population [ 1 ]. Approximately 30–40% of patients develop end-stage kidney disease within 20–30 years after their initial clinical presentation [ 2 ]. IgAVN …

  3. 14-02-2024 | IgA Vasculitis | ReviewPaper

    A rare twist: COVID-19 infection masquerading as IgA vasculitis in a hemophilia a patient

    Hemophilia A and B are one of the most common hereditary bleeding disorders. Patients are predisposed to bleeding spontaneously or after minor trauma in different areas such as the skin, gastrointestinal, or joints. COVID-19 infection has been …

  4. 15-01-2024 | Nephrotic Syndrome | Letter

    Tonsillectomy combined with intravenous methylprednisolone pulse for Japanese children with severe IgA vasculitis with nephritis—authors’ reply

  5. 07-11-2023 | Tonsillectomy | Letter

    Initial treatment with tonsillectomy combined with intravenous methylprednisolone pulse — another option for Japanese children with severe nephrotic IgA vasculitis with nephritis

  6. Open Access 01-12-2023 | IgA Vasculitis | OriginalPaper

    Rituximab as possible therapy in TNF inhibitor-induced IgA vasculitis with severe renal involvement

    Over the years tumor necrosis factor (TNF) inhibitor therapy has proven to be an effective treatment for chronic inflammatory diseases with a good safety profile. However, with the increase in patients receiving anti-TNF therapy and longer …

  7. 22-08-2023 | Hydroxychloroquine | Letter

    Hydroxychloroquine reduces proteinuria in Chinese patients with IgA vasculitis nephritis

  8. Open Access 27-09-2023 | IgA Vasculitis | ReviewPaper

    A narrative review of potential drug treatments for nephritis in children with IgA vasculitis (HSP)

    Immunoglobulin A (IgA) vasculitis (IgAV, also known as Henoch-Schoenlein purpura, HSP) is the most common vasculitis of childhood. It usually presents with a simple, self-limiting disease course; however, a small subset of patients may develop …

  9. Open Access 01-12-2023 | IgA Vasculitis | OriginalPaper

    Comparative study on clinicopathological features and prognosis of IgA vasculitis nephritis and IgA nephropathy in children

    IgA vasculitis (IgAV), a prominent type of vasculitis among pediatric populations, is marked by its capacity to impact small blood vessels in multiple organs, including the skin, and is distinguished by the presence of immunofluorescent IgA

  10. Open Access 01-12-2022 | IgA Vasculitis | OriginalPaper

    Early clinical course of biopsy-proven IgA vasculitis nephritis

    IgA vasculitis (IgAV; formerly known as Henoch-Schönlein purpura) is the most common vasculitis in childhood with a peak incidence at 4–7 years [ 1 ]. Renal involvement occurs in 30–60% of the patients [ 2 ]. The majority of these patients presents …

  11. 26-07-2022 | IgA Vasculitis | Report

    IgA Vasculitis

  12. Open Access 01-12-2023 | IgA Vasculitis | OriginalPaper

    A case series on recurrent and persisting IgA vasculitis (Henoch Schonlein purpura) in children

    IgA vasculitis (IgAV, formerly Henoch Schonlein purpura, HSP) is the most common vasculitis encountered in childhood with an estimated incidence of 27.2 per 100,000 children in the U.K [ 1 ]. It usually presents as a purpuric non-blanching rash …

  13. 17-06-2022 | IgA Vasculitis | BriefCommunication

    IgA vasculitis with underlying monoclonal IgA gammopathy: innovative therapeutic approach targeting plasma cells. A case series

    Immunoglobulin A vasculitis (IgAV) is a systemic vasculitis with predominant polyclonal IgA1 immune complex deposits [ 1 , 2 ]. Vascular purpura, arthralgia, glomerulonephritis, and/or gastrointestinal (GI) involvement are the main clinical …

  14. Open Access 14-06-2023 | IgA Vasculitis | OriginalPaper

    Clinical course and management of children with IgA vasculitis with nephritis

    IgA vasculitis (IgAV) (formerly Henoch-Schönlein purpura or HSP) is the most common vasculitis seen in children, with an incidence of 6–20 cases per 100,000 children per year [ 1 ]. IgAV affects small vessels and presents with palpable purpuric …

  15. Open Access 01-12-2023 | Human Immunodeficiency Virus | OriginalPaper

    Cytomegalovirus colitis unmasking human immunodeficiency virus infection as a cause of IgA vasculitis

    Human immunodeficiency virus (HIV) is a rare and frequently neglected cause of autoimmune rheumatic diseases, including vasculitides, and may complicate their clinical course [ 1 ]. The presence of unusual features like an autoimmune condition …

  16. Open Access 13-10-2022 | IgA Vasculitis | OriginalPaper

    Urinary complement proteins are increased in children with IgA vasculitis (Henoch-Schönlein purpura) nephritis

    Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the most common form of vasculitis in children with an estimated incidence of around 20 cases per 100,000 children per year. It is caused by deposition of …

  17. 29-06-2023 | IgA Vasculitis | OriginalPaper

    Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis

    Henoch–Schönlein purpura, recently also known as IgA vasculitis (IgAV), is the most common cause of vasculitis in childhood [ 1 ]. It is diagnosed based on palpable purpura, abdominal pain/bloody stools, and arthritis/arthralgia. The long-term …

  18. 26-05-2023 | IgA Vasculitis | BriefCommunication

    The lymph node in IgA vasculitis (Henöch-Schonlein purpura)

  19. 14-02-2022 | IgA Vasculitis | OriginalPaper

    A case of pathologically confirmed streptococcal infection-related IgA vasculitis with associated glomerulonephritis and leukocytoclastic cutaneous vasculitis

    We report the case of an 80 year-old woman who developed bilateral lower extremity purpura and renal impairment with proteinuria a few days after a transient fever (day 0). High levels of both anti-streptolysin-O antibody (ASO) and …

  20. 01-10-2021 | IgA Vasculitis | ReviewPaper

    IgA vasculitis

    IgA vasculitis (IgAV) is an inflammation of small vessels caused by perivascular deposition of IgA and activation of neutrophils. It may present as systemic vasculitis (IgAV - Henoch-Schönlein purpura) or as a variant restricted to the skin …

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