Results 251 to 260 of about 18,324 (292)
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Current Paediatrics, 2006
Summary This review summarises the evidence from the latest published research on the epidemiology, aetiology, pathophysiology, clinical manifestations, treatment, and prognosis of Henoch–Schonlein purpura (HSP). Analysis of the literature indicates the importance of genetic and infectious aetiologic considerations in the development of HSP.
S.E. Tarvin, Susan H. Ballinger
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Summary This review summarises the evidence from the latest published research on the epidemiology, aetiology, pathophysiology, clinical manifestations, treatment, and prognosis of Henoch–Schonlein purpura (HSP). Analysis of the literature indicates the importance of genetic and infectious aetiologic considerations in the development of HSP.
S.E. Tarvin, Susan H. Ballinger
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Bullous Henoch Schonlein purpura
Archives of Disease in Childhood, 2012We report a case of haemorrhagic bullous lesions in Henoch Schonlein purpura (HSP). A 9-year-old girl presented with 2 days of right knee pain and a purpuric rash on her legs and …
Meriel Raymond, Joanne Spinks
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Henoch−Schonlein purpura and pulmonary tuberculosis
Pediatrics International, 2002WOS: 000177950500018 PubMed: 12225561 …
Islek, I +4 more
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Current Opinion in Rheumatology, 2003
The purpose of this review is to educate the reader about the one of the most common vasculitides of childhood: Henoch-Schonlein purpura. Although the disease has been described for over a century, the etiology has yet to be discovered. Adult-onset Henoch-Schonlein purpura is unusual, but through case studies, this review examines some of the common ...
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The purpose of this review is to educate the reader about the one of the most common vasculitides of childhood: Henoch-Schonlein purpura. Although the disease has been described for over a century, the etiology has yet to be discovered. Adult-onset Henoch-Schonlein purpura is unusual, but through case studies, this review examines some of the common ...
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The role of chemokines in Henoch Schonlein Purpura
Rheumatology International, 2007The pathogenesis of Henoch Schonlein Purpura is incompletely understood and the role of chemokines is unknown.To investigate the levels of CC chemokines, eotaxin, TARC, and CXC chemokine IP-10 in Henoch Schonlein Purpura.Three groups of children were enrolled in the study: Henoch Schonlein Purpura in active stage (n = 26), Henoch Schonlein Purpura in ...
Poyrazoglu, H +4 more
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Pancreatitis as a Complication of Henoch–Schonlein Purpura
Journal of Pediatric Gastroenterology and Nutrition, 1982A 5‐year‐old girl suffering from Henoch–Schonlein purpura developed severe abdominal pain accompanied by vomiting and fever. Concomitantly, the serum amylase level became elevated and leukocytosis developed, with a shift to the left. A diagnosis of pancreatitis complicating Henoch–Schonlein purpura was made.
Doron Roll +4 more
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Pleural haemorrhage in Henoch Schonlein purpura
Clinical Rheumatology, 1993We describe a seven-year old boy with Henoch-Schonlein purpura who presented with extensive skin rash, arthritis, and persistent abdominal pain. He was found to have small intestinal submucosal and subserosal haemorrhage on exploratory laparatomy.
N. K. Qaddoumi, Mohammed Hammoudeh
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Penile involvement in Henoch-Schonlein purpura [PDF]
The Indian Journal of Pediatrics, 2002 The authors report the case of a four-year-old boy who, having been diagnosed as having uncomplicated Henoch-Schonlein purpura, returned five days later with a new crop of lesions and sudden onset of engorgement and oedema of the penis. Testicular and scrotal involvement has been well documented in Henoch-Schonlein purpura but involvement of the penis ...
R. Ramanan, D. Shah, JM Sandell
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2018
Henoch–Schonlein purpura, also known as “IgA vasculitis” or “anaphylactoid purpura,” is a multisystem small-vessel vasculitis characterized by deposition of immune complexes containing immunoglobulin A and subsequent complement activation. HSP primarily affects the skin, joints, gastrointestinal tract, and renal system.
Fatemah Mamdani, Suzanne K. W. Mankowitz
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Henoch–Schonlein purpura, also known as “IgA vasculitis” or “anaphylactoid purpura,” is a multisystem small-vessel vasculitis characterized by deposition of immune complexes containing immunoglobulin A and subsequent complement activation. HSP primarily affects the skin, joints, gastrointestinal tract, and renal system.
Fatemah Mamdani, Suzanne K. W. Mankowitz
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Intussusception associated with Henoch-Schonlein purpura
The Journal of Emergency Medicine, 1991Henoch-Schonlein purpura is a clinical diagnosis, based on a presentation including rash, arthralgia/arthritis, and abdominal pain, often with renal complications. A rare complication is intussusception, presumably initiated by an edematous vasculitic leading point in the small bowel's mucosal surface.
Daniel F. Danzl, Katherine J. Little
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