Results 21 to 30 of about 15,099 (182)
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
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Multi-omics Research Progress of IgA Vasculitis [PDF]
Zhongguo quanke yixueIgA vasculitis is a common systemic small vasculitis in childhood. Its pathogenesis is mainly caused by IgA immune complex deposition, manifested as skin purpura with or without digestive tract injury, joint injury and kidney involvement.
QU Yaxue, DING Ying, HAN Shanshan, XU Shanshan
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Renal biopsy in children with IgA vasculitis [PDF]
Brazilian Journal of Nephrology, 2022 Abstract Introduction Henoch-Schönlein purpura nephritis (HSN) is defined as Henoch-Schönlein purpura with kidney involvement, including hematuria and/or proteinuria. The aim of this study was to evaluate the data of HSN patients who underwent renal biopsy, and compare the main clinical and laboratory parameters that may affect renal biopsy findings ...
Mehtap Akbalik Kara +3 more
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Rheumatology & Autoimmunity, 2022 Objective: To explore a possible association between systemic immunoglobulin A (IgA) vasculitis and RS3PE syndrome and to investigate specific treatment regimens for adults who present with IgA vasculitis with renal involvement.
Shawn Mathew +3 more
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Scientific Reports, 2022 A nomogram for assessing the risk of IgA vasculitis nephritis (originally termed Henoch–Schönlein purpura nephritis, HSPN) in IgA vasculitis (originally termed Henoch–Schönlein purpura, HSP) pediatric patients can effectively improve early diagnosis and ...
Yuna Bi +10 more
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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
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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
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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
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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
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IgA vasculitis with nephritis in children
Advances in Clinical and Experimental Medicine, 2020 Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura (HSP), is the most common form of systemic vasculitis in children. Although the first case of IgAV was described more than 200 years ago, its etiology still remains unclear. Nephrological symptoms are observed in 30-50% of children during the course of the disease, and in up
Katarzyna Dyga, Maria Szczepańska
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