Results 21 to 30 of about 220,566 (226)
IgA vasculitis update: Epidemiology, pathogenesis, and biomarkers
Frontiers in Immunology, 2022 Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the most common systemic vasculitis in children, characterized by diverse clinical manifestations with a wide spectrum ranging from isolated cutaneous vasculitis to ...
Liyun Xu, Yongzhen Li, Xiaochuan Wu
semanticscholar +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
Alcohol-Associated Immunoglobulin A Vasculitis: A Case Report and Review of the Literature
Dermatopathology, 2020 Immunoglobulin A (IgA)-mediated leukocytoclastic vasculitis is a cutaneous small-vessel vasculitis characterized by skin findings of palpable purpura. It may occur secondary to infections, neoplasms, drugs, and systemic conditions, although it is most ...
Pallavi Basu +3 more
doaj +1 more source
IgA Vasculitis Complicated by Both CMV Reactivation and Tuberculosis
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 +1 more source
IgA Vasculitis and C3 Glomerulonephritis: One Patient... Various Autoimmune Diseases
Gazeta Médica, 2022 Leucocytoclastic vasculitis refers to a small vessel vasculitis caused by immune complexes, infections and medications. IgA or IgM/IgG immune complexes can be found in direct immunofluorescence studies suggesting specific forms of leucocytoclastic ...
Ana Margarida Pedro Antunes Ferreira Gaudêncio +2 more
doaj +4 more sources
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
doaj +1 more source
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
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
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
doaj +1 more source