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Pathogenesis of IgA Vasculitis: An Up-To-Date Review
Frontiers in Immunology, 2021 Immunoglobin A (IgA) vasculitis (IgAV), formerly called the Henoch-Schönlein purpura (HSP), is a small vessel vasculitis, characterized by IgA1-dominant immune deposition at diseased vessel walls.
Yan Song +6 more
semanticscholar +1 more source
BMC Pediatrics, 2019 Background We have recognized 15 children with jSLE and the antecedent of IgA vasculitis (HSP). This association is not broadly present in the literature.
Chiharu Murata +7 more
doaj +1 more source
A case series on recurrent and persisting IgA vasculitis (Henoch Schonlein purpura) in children
Pediatric Rheumatology Online Journal, 2023 Background IgA vasculitis (IgAV) is a small vessel vasculitis that is more common in childhood. Very limited evidence exists on patients who experience an atypical disease course.
Julien Marro +3 more
semanticscholar +1 more source
Origin of poorly galactosylated IgA1 other than mucosa: a viewpoint from a report on patient with IgA vasculitis. [PDF]
Ren FailPatients presenting monoclonal gammopathy of renal significance (MGRS) and IgA vasculitis collectively have rarely been reported. This study reports one patient with monoclonal IgA and λ, and with IgA positive-mesangial proliferative glomerulonephritis ...
Huang M +8 more
europepmc +2 more sources
Adult-onset immunoglobulin A vasculitis
APIK Journal of Internal Medicine, 2021 We describe a case of adult-onset immunoglobulin A vasculitis (IgA vasculitis) presenting with cutaneous, renal and gastrointestinal manifestations without any evidence of articular involvement.
Megha Amarapur, Sangram Biradar
doaj +1 more source
Cryoglobulinaemic vasculitis: classification and clinical and therapeutic aspects [PDF]
, 2007 Cryoglobulinaemia may cause cutaneous vasculitis and glomerulonephritis, potentially leading to end stage renal failure. An important proportion of cryoglobulinaemias are secondary to hepatitis C virus infection.
Braun, Gerald S. +4 more
core +2 more sources
BMC Pediatrics, 2023 Background IgA vasculitis nephritis (IgAVN) and IgA nephropathy (IgAN) share several clinical and pathological characteristics, though distinctions also exist. Their interrelation, however, remains undefined.
Yan-li Lv +5 more
semanticscholar +1 more source
Cutaneous Manifestations in Inflammatory Bowel Diseases [PDF]
, 2015 Inflammatory bowel diseases have a high frequency in Europe. They are chronic disorders that evolve with relapses and remissions. Clinical features include the signs of underlying inflammatory bowel disease and also signs of extraintestinal ...
Benea, Vasile +6 more
core +6 more sources
Intravenous γ Globulin for Intractable Abdominal Pain due to IgA Vasculitis
Case Reports in Pediatrics, 2020 IgA vasculitis (formerly known as Henoch–Schönlein purpura or anaphylactoid purpura) is a usually benign vasculitis that affects children of school age. The disease is characterized by the tetrad of palpable purpura, arthralgia/arthritis, abdominal pain,
George Naifa +4 more
doaj +1 more source
IgA vasculitis nephritis (Schönlein-Henoch purpura with nephritis) following COVID-19 vaccination [PDF]
Journal of Nephropathology, 2023 IgA vasculitis nephritis (Schönlein-Henoch purpura nephritis) is an autoimmune circumstance characterized by palpable purpura involving the lower limbs, arthralgia, abdominal pain and kidney involvement.
Leila Mahmoodnia +11 more
doaj +1 more source