نتایج جستجو برای: cutaneous polyarteritis nodosa

تعداد نتایج: 56164  

Journal: :Annals of the rheumatic diseases 1995
L Kumar B R Thapa B Sarkar B N Walia

OBJECTIVE To report 10 children younger than 10 years of age with benign cutaneous polyarteritis nodosa (BCPAN). METHODS Ten children aged 1.25-10 years (mean 4.7 years; M:F = 7:3) were admitted with an unusual vasculitis. The clinical features, laboratory investigations, treatment and follow up data were analysed. RESULTS Clinical features of these patients included: fever (10), peripheral...

2002
P. Braeckman S. Joniau R. Oyen R. Croes H. Van Poppel

A 28-year-old man presented with a seven-day history of testicular pain. Physical examination revealed a mass in the lower pole of the left testis. This mass was a tumour suspect on scrotal ultrasound and MRI. Testicular tumour markers were negative. A radical orchidectomy was performed. Histologically, the diagnosis of polyarteritis nodosa (PAN) was made. Retrospectively, the diagnosis of PAN ...

Journal: :Annals of the rheumatic diseases 1993
G R Struthers M T Pugh D A Woodward

1 Graf M W, Uhr J W. Regulation of antibody formation by serum antibody. I. Removal of specific antibody by means of immunoadsorption. Exp Med 1969; 130: 1175-86. 2 Bystryn J C, Graf M W, Uhr J W. Regulation of antibody formation by serum antibody. II. Removal of specific antibody by means of exchange transfusion. Exp Med 1970; 132: 1279-87. 3 Verrier Jones J, Robinson M F, Parciany R K, Layfer...

Journal: :JAMA dermatology 2014
Mark G Kirchhof Agnes Y Y Lee Jan P Dutz

IMPORTANCE Biochemical markers of disease allow clinicians to monitor disease severity, progression, and response to treatment. C-reactive protein and erythrocyte sedimentation rate are commonly used biochemical markers of inflammatory disease. We present 2 cases that indicate that D-dimer levels may be useful as a potential biochemical marker of disease activity in certain cutaneous inflammato...

Journal: :The British journal of ophthalmology 1945
R Sampson

2012

The renal involvement is common in any form of systemic vasculitis. These include classic polyarteritis nodosa, Wegener’s granulomatosis, microscopic polyarteritis, Churg-Strauss syndrome, and the hypersensitivity vasculitides (including Henoch-Schönlein purpura, mixed cryoglobulinemia, and serum sickness). Also vascultitis secondary to rheumatological disorders such as rheumatoid arthritis can...

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