Results 31 to 40 of about 23,138 (242)
Cutaneous Manifestations in Inflammatory Bowel Diseases [PDF]
Inflammatory bowel diseases have a high frequency in Europe. They are chronic disorders that evolve with relapses and remissions. Clinical features include the signs of underlying inflammatory bowel disease and also signs of extraintestinal ...
Benea, Vasile+6 more
core +6 more sources
Adult-onset immunoglobulin A vasculitis
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
IgA Vasculitis during Atezolizumab Treatment
Yoshinao Ono+3 more
openalex +4 more sources
Cryoglobulinaemic vasculitis: classification and clinical and therapeutic aspects [PDF]
Cryoglobulinaemia may cause cutaneous vasculitis and glomerulonephritis, potentially leading to end stage renal failure. An important proportion of cryoglobulinaemias are secondary to hepatitis C virus infection.
Braun, Gerald S.+4 more
core +2 more sources
Association of Vasculitis and Familial Mediterranean Fever
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
Intravenous γ Globulin for Intractable Abdominal Pain due to IgA Vasculitis
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
IgA vasculitis nephritis (Schönlein-Henoch purpura with nephritis) following COVID-19 vaccination [PDF]
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
IgA vasculitis with nephritis in children
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
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+3 more
doaj +1 more source
What is new in the management of rapidly progressive glomerulonephritis? [PDF]
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