Results 31 to 40 of about 15,557 (223)
Increased Urinary IgA in Paediatric IgA Vasculitis Nephritis
International Journal of Molecular Sciences, 2022 IgA vasculitis (IgAV) is the most common form of paediatric vasculitis, with up to 50% of patients experiencing kidney inflammation. Much remains unknown about IgAV, but it is believed to arise due to galactose-deficient IgA1 promoting an auto-inflammatory response.
Julien Marro +4 more
openaire +2 more sources
IgA vasculitis presenting as nephrotic syndrome following COVID-19 vaccination: a case report
BMC Nephrology, 2022 Background Following the strong recommendation for coronavirus disease 2019 (COVID‑19) vaccination, many patients with medical comorbidities are being immunized.
Illeon Cho, Jwa-Kyung Kim, Sung Gyun Kim
doaj +1 more source
Hospital-onset IgA vasculitis triggered by infectious endocarditis
IDCases, 2023 This is a case of IgA vasculitis developed in the hospital during treatment of infective endocarditis. When purpura appears in a patient under IE treatment, we should consider IgA vasculitis as a differential diagnosis and check renal function.
Kento Furuya, Naoya Itoh
doaj +1 more source
Vasculitis IgA en el adulto. Informe de caso
Medisur, 2021 La vasculitis IgA, también conocida como púrpura de Schönlein-Henoch, es una vasculitis leucocitoclástica que involucra pequeños vasos con depósito de inmunocomplejos IgA. Puede abarcar piel, articulaciones, riñones y tracto gastrointestinal.
Samuel Sánchez Sánchez +2 more
doaj
Granulomatosis with Polyangiitis Misdiagnosed as IgA Vasculitis in a Child
Case Reports in Pediatrics, 2023 Background. Granulomatosis with polyangiitis (GPA) with early manifestations simulating IgA vasculitis is a very rare childhood systemic disease. Case Presentation.
Sheida Amini, Mohsen Jari
doaj +1 more source
IgA vasculitis (Henoch-Schönlein purpura) [PDF]
Dermatology Online Journal, 2015 We report the first case of direct immunoflourescence-proven immunoglobulin A (IgA) vasculitis associated with influenza infection in an adult patient. IgA vasculitis, which was previously known as Henoch-Schönlein purpura, is the most common systemic vasculitis in children but rarely occurs in adults. Disease onset often occurs after upper respiratory
Farhadian, Joshua A +5 more
openaire +4 more sources
IgA (Henoch Schönlein Purpura) Vasculitis in a Pediatric Patient with COVID-19 and Strongyloidiasis
Revista de la Facultad de Medicina Humana, 2021 Vasculitis is a rare disease in children, with IgA Vasculitis being its most common presentation. One condition that has been associated with the development of vasculitis is the invasion of the vascular endothelium by Strongyloides stercoralis in cases ...
Mayron David Nakandakari Gomez +2 more
doaj +1 more source
Frontiers in Medicine, 2022 ObjectiveThe frequency of vasculitis may be increased in patients with Familial Mediterranean Fever (FMF), according to several studies. Our aim was to assess the characteristics of French adult patients with both diseases.MethodsPatients with vasculitis
Salam Abbara +17 more
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Navigating the initial diagnosis and management of adult IgA vasculitis: A reviewCapsule Summary
JAAD International, 2022 Background: IgA vasculitis in adults has not been thoroughly studied. This has left a practice gap related to the management and follow-up of a population that is at an increased risk of comorbidities and potentially poor outcomes. For this reason, it is
Brenna G. Kelly, BA +5 more
doaj +1 more source
IgA Vasculitis and IgA Nephropathy: Same Disease? [PDF]
Journal of Clinical Medicine, 2021 Many authors suggested that IgA Vasculitis (IgAV) and IgA Nephropathy (IgAN) would be two clinical manifestations of the same disease; in particular, that IgAV would be the systemic form of the IgAN. A limited number of studies have included sufficient children or adults with IgAN or IgAV (with or without nephropathy) and followed long enough to ...
openaire +2 more sources