Results 51 to 60 of about 201,611 (277)

IgA Vasculitis Associated With COVID-19

Cureus, 2023
IgA vasculitis, also known as Henoch-Schonlein Purpura (HSP), is an inflammatory disorder of small blood vessels that can present with palpable purpura, arthralgias, abdominal pain, and kidney disease.
Yousef Salem, Zaryab Alam, M. Shalabi, G. Hosler, Sampada Acharya   +4 more
semanticscholar   +1 more source

What is new in the management of rapidly progressive glomerulonephritis? [PDF]

, 2015
Rapidly progressive glomerulonephritis (RPGN) results from severe crescentic damage to glomeruli and leads to irreversible kidney failure if not diagnosed and managed in a timely fashion.
Greenhall, GHB, Salama, AD
core   +1 more source

IgA vasculitis with nephritis in children

Advances in Clinical and Experimental Medicine, 2020
Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura (HSP), is the most common form of systemic vasculitis in children. Although the first case of IgAV was described more than 200 years ago, its etiology still remains unclear. Nephrological symptoms are observed in 30-50% of children during the course of the disease, and in up
Katarzyna Dyga, Maria Szczepańska
openaire   +2 more sources

Severe IgA vasculitis with features of remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome in a 60‐year‐old male treated with plasmapheresis

Rheumatology & Autoimmunity, 2022
Objective: To explore a possible association between systemic immunoglobulin A (IgA) vasculitis and RS3PE syndrome and to investigate specific treatment regimens for adults who present with IgA vasculitis with renal involvement.
Shawn Mathew, Rohan Goyal, Nealansh Gupta, Rauno Joks   +3 more
doaj   +1 more source

Development of IgA vasculitis with severe glomerulonephritis after COVID-19 vaccination: a case report and literature review

CEN Case Reports, 2022
With the worldwide spread of the COVID-19 vaccine program during the COVID-19 pandemic, the numbers of reported cases with new-onset or relapsed kidney disease/vasculitis such as minimal change nephrotic syndrome, immunoglobulinA (IgA) nephropathy, and ...
K. Sugita, Shuzo Kaneko, Rina Hisada, Makiko Harano, Emi Anno, Sou Hagiwara, E. Imai, Michio Nagata, Y. Tsukamoto   +8 more
semanticscholar   +1 more source

IgA vasculitis after COVID-19: a case-based review. [PDF]

Rheumatol Int
IgA-associated vasculitis (IgAV) known as Henoch - Schönlein purpura (HSP) disease is an inflammatory disorder of small blood vessels. It’s the most common type of systemic vasculitis in children which can be associated with the inflammatory process ...
Suszek D, Grzywa-Celińska A, Emeryk-Maksymiuk J, Krusiński A, Redestowicz K, Siwiec J.   +5 more
europepmc   +2 more sources

HLA Polymorphisms and Clinical Manifestations in IgA Vasculitis. [PDF]

Int J Mol Sci
Studies concerning the genetic background of IgA vasculitis (IgAV), a small-vessel vasculitis occurring predominantly in childhood, have confirmed that the HLA-DRB1 gene showed a strong association with disease susceptibility.
Held M, Stingl Jankovic K, Sestan M, Sapina M, Kifer N, Srsen S, Frkovic M, Gagro A, Grubic Z, Jelusic M.   +9 more
europepmc   +2 more sources

New Insights and Challenges Associated With IgA Vasculitis and IgA Vasculitis With Nephritis—Is It Time to Change the Paradigm of the Most Common Systemic Vasculitis in Childhood?

Frontiers in Pediatrics, 2022
What are the challenges ahead and how have we responded so far when it comes to the non-granulomatous systemic vasculitis, characterized mainly by deposits of IgA immune complexes in the endothelium of small blood vessels—IgA vasculitis (IgAV)?
M. Jelušić, M. Šestan, T. Giani, R. Cimaz   +3 more
semanticscholar   +1 more source

Biomarkers of IgA vasculitis nephritis in children [PDF]

PLOS ONE, 2017
Henoch-Schönlein purpura is a systemic vasculitis characterized by IgA deposits, which target the skin, joints, and kidneys, among other organs. In children, prognosis is often good but little is known about biomarkers of pediatric nephritis. We hypothesized that biological markers, including cytokines, immunoglobulins, IgA-immune complexes, IgA ...
Evangeline Pillebout, Agnès Jamin, Hamza Ayari, Pierre Housset, Melissa Pierre, Virginia Sauvaget, Denis Viglietti, Georges Deschenes, Renato C Monteiro, Laureline Berthelot, HSPrognosis group   +10 more
openaire   +6 more sources

Anti-phospholipid-antibodies in patients with relapsing polychondritis [PDF]

, 1998
Relapsing polychondritis (RP) is an extremly rare multisystemic disease thought to be of autoimmune origin. In order to assess if RP is associated with anti-phospholipid antibodies (aPL), clinical data and sera of 21 patients with RP were collected in a ...
B Lang, Balsa-Criado A, G Rauh, G Schmitz, Herman JH, J Schòlmerich, M Zeuner, Piette JC, Quere I, R H Straub, U Schlosser, Zeuner M   +11 more
core   +1 more source