Results 11 to 20 of about 24,135 (222)

IgA vasculitis

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, Cord Sunderkötter   +1 more
exaly   +5 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, Chao Liu, Ya-Li Zhang, Guo-Liang Li   +3 more
doaj   +3 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, Ana Martinez Gonzalez, Rosa Eva Bautista Alonso, Jose Miguel García Bruñén, Gonzalo Acebes Repiso   +4 more
doaj   +5 more sources

Landscape of intestinal microbiota in patients with IgA nephropathy, IgA vasculitis and Kawasaki disease

Frontiers in Cellular and Infection Microbiology, 2022
ObjectiveTo explore the common differential flora of IgAN, Kawasaki disease and IgA vasculitis by screening and analyzing the differential intestinal flora between the three disease groups of IgAN, Kawasaki disease and IgA vasculitis and their healthy ...
Xueli Hu, Ru Fan, Wenzhu Song, Jianbo Qing, Xiaoyan Yan, Yaheng Li, Qi Duan, Yafeng Li, Yafeng Li, Yafeng Li, Yafeng Li   +10 more
doaj   +3 more sources

IgA Vasculitis and IgA Nephropathy: Same Disease? [PDF]

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. A limited number of studies have included sufficient children or adults with IgAN or IgAV (with or without nephropathy) and followed long enough to ...
Evangeline Pillebout
openaire   +4 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, Juliana Russo Simon, Vivianne Saraiva Leitao Viana, Tamima Mohamad Abou Arabi, Vitor Cavalcanti Trindade, Ana Carolina Cortez Maia, Lara Regina Cavalcante Melo, Bianca Pires Ihara, Nadia Emi Aikawa, Clovis Artur Silva   +9 more
doaj   +5 more sources

IgA vasculitis associated with chronic myelomonocytic leukemia [PDF]

BMC Rheumatology
IgA 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, Francois Chasset, Noémie Abisror, Pierre Hirsch, Olivier Fain, Arsène Mékinian, on behalf of MINHEMON (French network on immune diseases associated with hemopathies and cancers)   +6 more
doaj   +2 more sources

Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study [PDF]

Kidney International Reports, 2018
Introduction: The Cure Glomerulonephropathy Network (CureGN) is a 66-center longitudinal observational study of patients with biopsy-confirmed minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, or IgA nephropathy (IgAN)
Ambruzs, Josephine M., Appel, Gerald B., Bomback, Andrew S., Cai, Yi, Cattran, Daniel C., Chishti, Aftab S., CureGN Consortium, D’Agati, Vivette D., D’Alessandri-Silva, Cynthia J., Falk, Ronald J., Flessner, Michael, Gbadegesin, Rasheed A., Gharavi, Ali G., Gillespie, Brenda W., Gipson, Debbie S., Greenbaum, Larry A., Guay-Woodford, Lisa M., Hogan, Jonathan J., Holzman, Lawrence B., Iragorri, Sandra, Jennette, J. Charles, Julian, Bruce A., Khalid, Myda, Kiryluk, Krzysztof, Kretzler, Matthias, Lafayette, Richard A., Liapis, Helen, Lugani, Francesca, Mansfield, Sarah A., Mason, Sherene, Matar, Raed Bou, Nachman, Patrick H., Nast, Cynthia C., Nester, Carla M., Noone, Damien G., Novak, Jan, O’Shaughnessy, Michelle M., Reich, Heather N., Rheault, Michelle N., Rizk, Dana V., Robinson, Bruce M., Saha, Manish K., Sanghani, Neil S., Selewski, David T., Smoyer, William E., Sperati, C. John, Sreedharan, Rajasree, Srivastava, Tarak, Swiatecka-Urban, Agnieszka, Twombley, Katherine, Vasylyeva, Tetyana L., Weaver, Donald J., Yin, Hong, Zee, Jarcy   +53 more
core   +3 more sources

Efficacy of Telitacicept in treating IgA vasculitis nephritis: a two-case report [PDF]

Frontiers in Immunology
Telitacicept, a B lymphocyte stimulator/A proliferation-inducing ligand dual-target fusion protein, mainly used for IgA nephropathy and systemic lupus erythematosus.
Shuang-xi Li, Rui-kang Hu, De-liang Kong, Jing Xu, Qi Bian, Zhi-Yong Guo, Xiao-bin Mei   +6 more
doaj   +2 more sources

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, Suha Abu Khalaf, Taylor Nelson   +2 more
doaj   +1 more source