Results 31 to 40 of about 24,135 (222)
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
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
A Case of Henoch-Schonlein Purpura Associated with Rotavirus Infection in an Elderly Asian Male and Review of the Literature. [PDF]
, 2017 BACKGROUND Henoch-Schönlein purpura (HSP), a small vessel vasculitis mediated by deposition of immune-complexes containing IgA in the skin, gut, and glomeruli, often presents with abdominal pain, purpuric rash in the lower extremities and buttocks, joint
Adderley +13 more
core +2 more sources
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
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 +11 more
core +1 more source
Pathologic manifestations of levamisole-adulterated cocaine exposure. [PDF]
, 2015 UnlabelledRheumatic manifestations of cocaine have been well described, but more recently, a dramatic increase in the levamisole-adulterated cocaine supply in the United States has disclosed unique pathologic consequences that are distinct from pure ...
Jen, Kuang-Yu, Nolan, Amber L
core +1 more source
Multi-omics Research Progress of IgA Vasculitis [PDF]
Zhongguo quanke yixueIgA vasculitis is a common systemic small vasculitis in childhood. Its pathogenesis is mainly caused by IgA immune complex deposition, manifested as skin purpura with or without digestive tract injury, joint injury and kidney involvement.
QU Yaxue, DING Ying, HAN Shanshan, XU Shanshan
doaj +1 more source
Intravenous γ Globulin for Intractable Abdominal Pain due to IgA Vasculitis
Case Reports in Pediatrics, 2020 IgA vasculitis (formerly known as Henoch–Schönlein purpura or anaphylactoid purpura) is a usually benign vasculitis that affects children of school age. The disease is characterized by the tetrad of palpable purpura, arthralgia/arthritis, abdominal pain,
George Naifa +4 more
doaj +1 more source