IgA Vasculitis Complicated by Both CMV Reactivation and Tuberculosis [PDF]
Pediatric Reports, 2021 Immunoglobulin A (IgA) vasculitis is the most common systemic vasculitis in the pediatric population. We present the case of a patient with IgA vasculitis with nephritis who developed cytomegalovirus (CMV) infection followed by Mycobacterium tuberculosis
Małgorzata Mizerska-Wasiak +5 more
doaj +2 more sources
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 +3 more sources
Patients With IgA Vasculitis and Kawasaki Disease Show Dysregulated Interferon Signature. [PDF]
Int J Rheum DisABSTRACT Objective IgA vasculitis (IgAV) and Kawasaki disease (KD) are the most common forms of childhood vasculitis. Although various factors such as viral infections, genetic factors, and environmental factors are involved in the development of both diseases, their pathogenesis remains unclear.
Varol SE +9 more
europepmc +2 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
doaj +5 more sources
IgA vasculitis associated with chronic myelomonocytic leukemia [PDF]
BMC RheumatologyIgA vasculitis is a predominantly pediatric autoimmune disease characterized by IgA deposit in small vessels. Chronic myelomonocytic leukemia (CMML) is a rare hematological malignancy classified within myelodysplastic syndromes.
Bénédicte Rouvière +6 more
doaj +2 more sources
Granulomatosis with Polyangiitis Misdiagnosed as IgA Vasculitis in a Child [PDF]
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 +2 more sources
Clinical and pathological differences between skin‐limited IgM/IgG vasculitis and skin‐limited IgA vasculitis [PDF]
Journal of Cutaneous Immunology and Allergy, 2021 Objectives Cutaneous IgM/IgG vasculitis (IgM/IgG V) is characterized by leukocytoclastic vasculitis histologically and by IgM‐ or IgG‐ perivascular deposition.
Miho Kawamura +6 more
doaj +2 more sources
Efficacy of Telitacicept in treating IgA vasculitis nephritis: a two-case report [PDF]
Frontiers in ImmunologyTelitacicept, a B lymphocyte stimulator/A proliferation-inducing ligand dual-target fusion protein, mainly used for IgA nephropathy and systemic lupus erythematosus.
Shuang-xi Li +6 more
doaj +2 more sources
Intermittent abdominal pain in IgA vasculitis [PDF]
Revista Paulista de Pediatria, 2021 Objective: To assess intermittent abdominal pain in IgA vasculitis patients and its relation to demographic data, clinical manifestations and treatments.
Izabel Mantovani Buscatti +9 more
doaj +6 more sources
Origin of poorly galactosylated IgA1 other than mucosa: a viewpoint from a report on patient with IgA vasculitis [PDF]
Renal FailurePatients 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 ...
Manxia Huang +8 more
doaj +2 more sources