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We present the first case of peliosis hepatis in a patient with a primary immunodeficiency, common variable immunodeficiency.
2
Peliosis hepatis is a rare condition characterized by blackish-blue blood-filled cavities in hepatic parenchyma caused by dilatation of hepatic sinusoids.
Usage of purpura in anglès
1
The skin necrosis in purpura fulminans often begins in the distal extremities.
2
The diagnosis of Henoch-Schonlein purpura was rapidly made and intensive steroid therapy started.
3
Cutaneous involvement usually includes palpable purpura or cutaneous to subcutaneous nodes.
4
Mackenzie reports an instance of hemophilic purpura of the retina, followed by death.
5
Such a complication of acute pancreatitis with Henoch-Schönlein purpura is rare.
6
We report here two cases of thrombocytopenic purpura at onset of Zika virus infection.
7
Disease followed on famine: typhus, cholera, and purpura raced unchecked through the weakened population.
8
None of patients have purpura, permanent pigmentation change and scarring.
9
A patient with aortic regurgitation and idiopathic thrombocytopenic purpura underwent a successful valve replacement.
10
This is the first report of infectious purpura fulminans in a protein C-deficient heterozygote.
11
The clinical picture varied from eczema through urticaria to purpura.
12
A 67-year-old man presented with fever, purpura and peripheral arthritis.
13
The risk for developing chronic idiopathic thrombocytopenic purpura was assessed using simple and multivariable analyses.
14
The patient's clinical course and the findings of a renal biopsy study revealed purpura nephritis.
15
There were no significant differences in the recurrence of Henoch-Schönlein purpura symptoms or gastrointestinal symptoms.
16
The case of a 68-year-old woman with purpura nephritis associated with nephrotic syndrome is herein described.