Results 21 to 30 of about 123,589 (210)
Salivary Immunoglobulin A (IgA) in children with IgA vasculitis [PDF]
Introduction: The local salivary immunoglobulin A (IgA) is the predominant immunoglobulin in the saliva and plays an important role in the local immune defence system.
Alomairi, Maryam
core +2 more sources
Diagnóstico y tratamiento de la Vasculitis por IgA [PDF]
, 2022 IgA vasculitis is a leukocytoclastic vasculitis, with a self-limited course, of autoimmune origin, mediated by IgA immune complexes. The ethiology of this disease is unknown, but the most common presentation is a paediatric patient that has been exposed ...
Leitón Solano, Valeria +2 more
core +2 more sources
Heparin-induced thrombocytopenia during IgA vasculitis: a case report [PDF]
, 2021 Immunoglobulin A (IgA) vasculitis is characterized by small vessel vasculitis involving immune complexes and IgA deposition. The development of heparin-induced thrombocytopenia (HIT) during IgA vasculitis is extremely rare.
Kyotani, Moe +4 more
core +1 more source
, 2023 Background Skin is frequently involved in small-vessel vasculitis. Based on immunofluorescence studies, it can be IgA type (Henoch-Schoenlein purpura) or IgA-negative type i.e. leukocytoclastic vasculitis.
Mohammad Ashraf Khan +3 more
core +1 more source
Immunoglobulin a (IgA) Vasculitis in the Elderly
Cureus, 2023 IgA vasculitis is a small vessel vasculitis mediated by the deposition of IgA immune complexes. It mostly occurs in children and is rare in adults, with increased severity and mortality in the latter. Its aetiology remains largely unknown, and its prognosis depends primarily on the extent of renal involvement. We present the case of a 71-year-old woman
Girao, Adriana +3 more
openaire +2 more sources
BMC Pediatrics, 2019 Background We have recognized 15 children with jSLE and the antecedent of IgA vasculitis (HSP). This association is not broadly present in the literature.
Chiharu Murata +7 more
doaj +1 more source
Abnormal urinalysis on day 7 in patients with IgA vasculitis (Henoch–Schönlein purpura) [PDF]
, 2016 2016-11Rare progression to renal failure imposes a burden on children with IgA vasculitis (Henoch–Schönlein purpura, HSP). An abnormal urinalysis on day 7 (7d-UA) may be a surrogate marker for persistent nephritis, but this has not been established.
Kawada, Jun-ichi +9 more
core +1 more source
Vaccines, 2022 IgA vasculitis is an immune complex-mediated small-vessel vasculitis that mainly occurs in children and is characterized by palpable purpura, arthralgia, abdominal pain, and glomerulonephritis.
Yunjung Choi +3 more
doaj +1 more source
Adult-onset immunoglobulin A vasculitis
APIK Journal of Internal Medicine, 2021 We describe a case of adult-onset immunoglobulin A vasculitis (IgA vasculitis) presenting with cutaneous, renal and gastrointestinal manifestations without any evidence of articular involvement.
Megha Amarapur, Sangram Biradar
doaj +1 more source
Association of Vasculitis and Familial Mediterranean Fever
Frontiers in Immunology, 2019 Certain types of vasculitis occur more frequently and present differently in patients with familial Mediterranean fever (FMF). We assessed the characteristics of patients with FMF and systemic vasculitis through a systematic review of the literature ...
Salam Abbara +4 more
doaj +1 more source