Results 171 to 180 of about 123,589 (210)

IgA Vasculitis and IgA Nephropathy: Same Disease?

Journal of Clinical Medicine, 2021
Many authors suggested that IgA Vasculitis (IgAV) and IgA Nephropathy (IgAN) would be two clinical manifestations of the same disease; in particular, that IgAV would be the systemic form of the IgAN.
Évangéline Pillebout
exaly   +2 more sources

Intestinal Permeability and IgA Provoke Immune Vasculitis Linked to Cardiovascular Inflammation [PDF]

Immunity, 2019
Recent experimental data and clinical, genetic, and transcriptome evidence from patients converge to suggest a key role of interleukin-1β (IL-1β) in the pathogenesis of Kawasaki disease (KD).
Magali Noval Rivas, Michifumi Yamashita, Angela C Gomez   +2 more
exaly   +2 more sources

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IgA vasculitis induced by acenocoumarol

Reumatología Clínica (English Edition), 2020
We present the case of a 73-year-old man with IgA vasculitis after administration of acenocoumarol, confirmed by anatomopathological study. He had cutaneous, joint and renal involvement. With the reintroduction of the drug, the clinical manifestations worsened. They were completely resolved with its suspension, without additional maintenance treatment.
Sara, Esteban Terradillos, José Gabriel, Erdozain Castiella, Juan Manuel, Goiri Aparicio, Juan Antonio, Ratón Nieto, Aitor, Fernández Larrinoa Santamaria, Juan, Monte Armenteros   +5 more
openaire   +2 more sources

Multisystemic manifestations of IgA vasculitis

Clinical Rheumatology, 2020
Immunoglobulin A vasculitis (IgAV), also known as Henoch-Schönlein Purpura, is one of the most common kind of systemic vasculitis in children, and due to the involvement of small blood vessels throughout the body, this disease can cause a variety of symptoms in different organs. Our aim was to review the data on various systemic manifestations of IgAV.
Lina Du, Panpan Wang, Chang Liu, Shaojing Li, Shuang Yue, Yan Yang   +5 more
openaire   +2 more sources

IgA vasculitis with severe renal manifestation

BMJ Case Reports, 2022
IgA vasculitis is a rare systemic vasculitis in adults, frequently more severe than in paediatric age. It manifests with cutaneous, articular, gastrointestinal and renal involvement. We present a case of a man in his 40s diagnosed with IgA vasculitis with cutaneous, joint, gastrointestinal and renal disease.
Joana, Marques Dias, Marta Azevedo, Ferreira, Ana, Grilo, Fernando Martos, Gonçalves   +3 more
openaire   +2 more sources

Serum levels of galactose-deficient IgA1 in Chinese children with IgA nephropathy, IgA vasculitis with nephritis, and IgA vasculitis

Clinical and Experimental Nephrology, 2020
IgA nephropathy (IgAN) and IgA vasculitis with nephritis (IgAV-N) are related diseases. Galactose-deficient IgA1 (Gd-IgA1) plays an important role in the pathology of IgAV-N and IgAN, so we aim to compare the serum levels of Gd-IgA1 in Chinese pediatric patients with IgAN, IgAV-N, and IgAV.We retrospectively enrolled 52 patients with IgAN, 57 patients ...
Mengmeng, Tang, Xue, Zhang, Xueqian, Li, Lei, Lei, Hejia, Zhang, Chen, Ling, Jie, Ni, Jicheng, Lv, Xiaorong, Liu, Xiangmei, Chen   +9 more
openaire   +2 more sources

IgA Vasculitis

Journal of General Internal Medicine, 2022
Natalie Garcia, Victoria Jiminez, Alonso Heudebert   +2 more
openaire   +2 more sources

IgA vasculitis

QJM: An International Journal of Medicine, 2023
T, Tadokoro, T, Abe, T, Nakano, Y, Kimura, K, Higaki, S, Hayashidani, H, Tashiro   +6 more
openaire   +2 more sources

IgA Vasculitis in Adults

Current Treatment Options in Rheumatology, 2018
Immunoglobulin A vasculitis (IgAV) is a small vessel vasculitis with skin, joint, gastrointestinal and renal manifestations. Our understanding of the natural history of this disease is limited due to the overall low incidence of IgAV in adults and a lack of consensus regarding diagnostic criteria.
Sarah M. Moran, Heather N. Reich
openaire   +1 more source

Navigating Adult-Onset IgA Vasculitis-Associated Nephritis

Life
Purpose of Review: IgA vasculitis (IgAV), formerly Henoch–Schonlein purpura, is the most common systemic vasculitis in childhood. In adults, however, this condition is poorly understood, yet associated with more severe disease and poorer outcomes ...
Gek Cher Chan, Zi Yun Chang
exaly   +2 more sources