Results 181 to 190 of about 8,434 (216)
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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
openaire   +3 more sources

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
openaire   +1 more source

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
openaire   +2 more sources

Pancreatitis as a Complication of Henoch–Schonlein Purpura

Journal of Pediatric Gastroenterology and Nutrition, 1982
A 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.
D, Branski   +4 more
openaire   +2 more sources

Unusual manifestations of henoch-schonlein purpura

The Indian Journal of Pediatrics, 1984
Henoch schonlein syndrome (HSP) represents a diagnostic challenge when gastrointestinal symptoms or other atypical symptoms precede the cutaneous manifestations. We describe two patients whose abdominal symptoms antedated cutaneous manifestations. Six-year-old, black male patient, presented with 1 wk history of vomiting (without diarrhea or urinary ...
S P, Samuel, E, John, F, Assadi, S, Rao
openaire   +2 more sources

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
openaire   +2 more sources

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
openaire   +2 more sources

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
openaire   +2 more sources

Henoch-Schonlein purpura

1995
There are no available figures for this condition, but it is not an especially common disorder. Nevertheless, when it does occur the signs and symptoms are sufficiently severe to cause alarm and — at times — difficulties in diagnosis.
openaire   +1 more source

Functional Intestinal Obstruction in Henoch-Schonlein Purpura

Journal of Pediatric Gastroenterology and Nutrition, 1991
SummaryTwo patients with Henoch‐Schonlein purpura are described. Both developed prolonged intestinal obstruction requiring total parenteral nutrition. One child had transient partial duodenal obstruction on barium study and in the other extensive ecchymosis was confirmed at laparotomy.
N, Sharief, H C, Ward, C B, Wood
openaire   +2 more sources

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