Modern features of the evolution of IgA-vasculitis in children according to catamestic study
Актуальні проблеми сучасної медицини, 2021 . There is a tendency to an increase in the frequency of hospitalization of children with mixed forms of IgA-vasculitis with pronounced abdominal syndrome and involvement in the pathological process of the kidneys, which is possibly associated with an ...
Olena Kvacheniuk, Olena Okhotnikova
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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
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Blistering eruptions with tissue eosinophilia in a child with IgA vasculitis [PDF]
Clinical Case Reports, 2018 Key Clinical Message We present a child with bullous IgA vasculitis. Because skin biopsy showed epidermal vesicles with neutrophil infiltration and leukocytoclastic vasculitis in all layers of the dermis, with IgA deposits and tissue eosinophilia ...
Toru Watanabe, Shinya Tsukano
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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
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Case Report: Refractory hidradenitis suppurativa complicated by IgA vasculitis with nephritis: successful long-term control with surgery and bimekizumab [PDF]
Frontiers in ImmunologyHidradenitis suppurativa (HS) is a chronic inflammatory skin disease that can rarely be complicated by systemic immune phenomena. We report a 41-year-old woman with severe HS refractory to adalimumab who developed fever, palpable purpura, and renal ...
Ayaka Yasuda +3 more
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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
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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
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P129 IgA vasculitis with severe gastrointestinal and renal involvement: a case report of atypical pediatric presentation [PDF]
Rheumatol Adv PractIrfan Nengroo
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Seminars in Immunopathology, 2021 IgA vasculitis (IgAV) is an inflammation of small vessels caused by perivascular deposition of IgA and activation of neutrophils. It may present as systemic vasculitis (IgAV - Henoch-Schönlein purpura) or as a variant restricted to the skin (skin-limited IgAV), while IgA nephropathy presents a variant restricted to the kidneys.
Evangéline Pillebout +1 more
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Immunoglobulin A vasculitis induced by atypical pneumonia infection with Chlamydophila pneumonia
IDCases, 2022 Infections are a common trigger for IgA vasculitis. Among the bacteria that cause atypical pneumonia, Mycoplasma pneumoniae infection has strongly been associated with IgA vasculitis, with Chlamydophila pneumoniae reported with IgA vasculitis in only one
Seung Ah Kang +2 more
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