نتایج جستجو برای: schönlein purpura hsp

تعداد نتایج: 16817  

2008
Eleni Georgaki-Angelaki Stavroula Kostaridou Athanasia Lourida C. Petraki Evagelia Lagona

Henoch-Schönlein purpura glomerulonephritis (HSP-GN) is a common form of systemic small vessel vasculitis in children. Although prognosis is usually favourable, the disease is occasionally associated with a risk of renal insufficiency. Various immunosuppressive agents have been used in patients with severe HSP-GN, but none have shown convincing favourable effects. We report a case of biopsy-pro...

2008
Nigel D. Toussaint Michael Desmond Prue A. Hill

Henoch-Schönlein purpura (HSP) is a systemic vasculitis predominantly occurring in prepubertal children and characterised by a purpuric rash on the lower extremities, arthralgia and abdominal pain. Renal involvement is not uncommon affecting between 20 and 80% of patients [1] and severe nephrotic syndrome or nephritis is frequently associated with significant renal disease, morbidity and mortal...

Journal: :Anales de pediatria 2000
S A Bakkaloğlu M Ekim N Tümer G Deda I Erden T Erdem

Henoch-Schönlein purpura (HSP) is the most common systemic vasculitis of childhood, affecting the small blood vessels. The disease is a clinical syndrome characterized by multiple organ involvement including the skin, joints, gastrointestinal tract, and the kidneys. Headache and behavioral changes can be frequently seen during the course of the disease, but severe neurological signs such as sei...

Journal: :Fukushima journal of medical science 2013
Yukihiko Kawasaki Atsushi Ono Shinichiro Ohara Yuichi Suzuki Kazuhide Suyama Junzo Suzuki Mitsuaki Hosoya

Henoch-Schönlein purpura (HSP) is a systemic disorder characterized by leukocytoclastic vasculitis involving the capillaries and the deposition of IgA immune complexes. Renal involvement is the principal cause of morbidity and mortality in children with HSP. Thus, it is important to clarify the onset mechanism as well as the prognostic factors of Henoch-Schönlein purpura nephritis (HSPN) and to...

1996
Ayako Nakamura Tatsuo Fuchigami Yasuji Inamo

The gastrointestinal manifestations of Henoch-Schönlein purpura include abdominal pain, gastrointestinal bleeding, intussusception, and perforation. Protein-losing enteropathy is rarely associated with Henoch-Schönlein purpura. Two pediatric patients with Henoch-Schönlein purpura who developed protein-losing enteropathy are reported. Tc-99m human serum albumin scintigraphy is useful in the dete...

2015
Hyun Sik Kang Hee Sup Chung Ki-Soo Kang Kyoung Hee Han

INTRODUCTION Henoch-Schönlein purpura is an immunoglobulin A-mediated, small vascular inflammatory disease that can be associated with palpable purpura, arthralgia, abdominal pain, or nephritis. The presence of purpura facilitates the diagnosis of Henoch-Schönlein purpura at the onset of associated symptoms, whereas the absence of purpura makes the diagnosis challenging. It is important to diag...

2014
Reni Ghrahani Masayu Amanda Ledika Gartika Sapartini Budi Setiabudiawan

BACKGROUND Henoch-Schönlein purpura (HSP) is the most common vasculitis in children, characterized by triad of symptoms; palpable purpura without thrombocytopenia, abdominal pain, and arthritis. Renal involvement often occur in children with HSP. No data on the renal involvement of children with HSP in Indonesia, especially West Java. OBJECTIVE To evaluate renal involvement in children with H...

2012
Stanislas Bataille Aurélie Daumas Anne-Marie Tasei Noémie Jourde-Chiche Bertrand Dussol Stéphane Burtey Solène Taugourdeau Yvon Berland Laurent Chiche

INTRODUCTION Henoch-Schönlein purpura is a small-vessel systemic vasculitis. Although its exact pathophysiology remains unknown, Henoch-Schönlein purpura has been reported in association with various medical conditions including hypersensitivity. We report the case of a patient with vancomycin-induced Henoch-Schönlein purpura. CASE PRESENTATION A 42-year-old Caucasian man who had previously u...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1998
A C Allen F R Willis T J Beattie J Feehally

BACKGROUND Glomerular deposition of IgA1 is a common feature of Henoch-Schönlein purpura, and is indistinguishable from that seen in IgA nephropathy. Serum IgA1 is abnormally O-glycosylated in IgA nephropathy, and this may contribute to mesangial IgA1 deposition and the development of glomerular injury. This altered O-glycosylation of IgA1 can be detected by its increased binding to the lectin ...

Journal: :Lancet 1997
G D Schott

disorders. J Rheum 1992; 19: 721–28. 2 Mills JA, Michel BA, Bloch DA, et al.The American College of Rheumatology 1990 criterial for classification of Henoch-Schönlein purpura. Arthr Rheum 1990; 33: 1114–21. 3 Tancrede-Bohin E, Ochonisky S,Vignon-Pennamen M, Flaheul B, Morel P, Rybojad M. Henoch-Schönlein purpura in adult patients. Arch Dermatology 1997; 133: 438–42. 4 Blanco R, Martinez-Taboada...

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