Results 131 to 140 of about 3,384 (157)
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Henoch–Schonlein purpura

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 Ballinger
openaire   +1 more source

Henoch–Schonlein Purpura

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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Case 127: Henoch-Schonlein Purpura

Radiology, 2007
Pamela T. Johnson, MD Karen M. Horton, MD Elliot K. Fishman, MD History A 37-year-old man presented to his physician with sharp and continuous upper abdominal pain. Upper endoscopy was performed for evaluation and revealed Helicobacter pylori–negative gastritis. Treatment with a proton pump inhibitor failed to alleviate his symptoms.
Pamela T, Johnson   +2 more
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Henoch−Schonlein purpura and pulmonary tuberculosis

Pediatrics International, 2002
WOS ...
Islek, I   +4 more
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Intussusception associated with Henoch-Schonlein purpura

The Journal of Emergency Medicine, 1991
Henoch-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.
K J, Little, D F, Danzl
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Henoch schonlein purpura with rheumatic carditis

The Indian Journal of Pediatrics, 2004
Henoch Schonlein Purpura with acute rheumatic carditis is a rare entity and only few cases have been reported. An 8 year-old-girl presented with abdominal pain, arthralgia and rashes and was diagnosed as a case of Henoch Schonlein Purpura. She was managed conservatively and discharged.
Taruna, Gulati   +3 more
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Endothelin levels in Henoch-Schonlein purpura

Pediatric Nephrology, 2002
Henoch-Schonlein purpura (HSP) is one of the most common types of vasculitis disorders seen in childhood and is characterized by a rash, arthritis, abdominal pain, and renal involvement. Although HSP is an immunoglobulin A (IgA) related immune complex disease, the pathogenesis has not been fully elucidated.
Ali, Muslu   +7 more
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Pleural haemorrhage in Henoch Schonlein purpura

Clinical Rheumatology, 1993
We 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.
M, Hammoudeh, N K, Qaddoumi
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Henoch-schonlein purpura; orofacial presentation

British Journal of Oral and Maxillofacial Surgery, 1984
Henoch-Schonlein purpura is a relatively common syndrome that is associated with gastrointestinal symptoms, polyarthritis, erythemato-urticarial rashes and acute glomerulonephritis. A case is reported in which the initial manifestation was orofacial purpura.
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Penile involvement in Henoch-Schonlein purpura

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 ...
J, Sandell, R, Ramanan, D, Shah
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