Results 11 to 20 of about 123,589 (210)
IgA nephropathy with leucocytoclastic vasculitis [PDF]
Journal of International Medical Research, 2018 Leucocytoclastic vasculitis is a rare type of allergic disease caused by immune complexes. IgA nephropathy is a glomerulopathy characterized by recurrent episodes of gross haematuria or microscopic haematuria and IgA deposition in the glomerular ...
Lin-Yan Wei +3 more
doaj +4 more sources
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
doaj +2 more sources
Increased Urinary IgA in Paediatric IgA Vasculitis Nephritis [PDF]
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 ...
Edwards, Samuel +4 more
core +5 more sources
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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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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Vasculitis IgA en el adulto. Informe de caso [PDF]
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 +1 more source
Annular leukocytoclastic vasculitis: a new feature of IgA vasculitis [PDF]
European Journal of Case Reports in Internal MedicineBackground: Annular erythema is a rare manifestation of leukocytoclastic vasculitis. It may be associated with various drugs, infections, malignancies, or systemic diseases. Case description: A 36-year-old woman with no personal medical history presented
Cyrus Moini +5 more
core +4 more sources
Food-induced IgA Vasculitis (Henoch-Schönlein Purpura) [PDF]
European Journal of Case Reports in Internal Medicine, 2017 Immunoglobulin A (IgA) vasculitis is a rare entity in adults. It can be triggered by allergens such as drugs, food, or insect bites. We present a case of an adult male with a cutaneous IgA vasculitis of palpable purpura after eating canned sardines.
Javier Moreno Díaz +4 more
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Henoch–Schönlein Purpura (IgA Vasculitis) in Association with Thyrotoxicosis
Case Reports in Endocrinology, 2021 Graves’ disease is the most common cause of hyperthyroidism, which is characterized by thyroid antibodies and the following clinical manifestations: goiter, ophthalmopathy, and pretibial myxedema.
Mojgan Sanjari +2 more
doaj +2 more sources
IgA vasculitis in an adult diabetic male with rapidly progressive glomerulonephritis: A case study
Journal of Acute DiseaseRationale: IgA vasculitis or Henoch-Schonlein purpura is an immune complex mediated small vessel vasculitis characterized by clinical triad of arthritis, palpable purpura and gastrointestinal symptoms.
Varsha Luthra +4 more
doaj +2 more sources