Polyarteritis nodosa developing after discoid lupus erythematosus.

نویسندگان

  • E Letellier
  • H Longhurst
  • S J Diaz-Cano
  • D D'Cruz
چکیده

We describe a patient with discoid lupus erythematosus whose pattern of disease evolved into a systemic vasculitis polyarteritis nodosa.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Lupus Erythematosus and Collagen Diseases

the Connective tissues". The well known conditions described under group of the Collagen Diseases at present are : Rheumatic Diseases, Polyarteritis Nodosa, Disseminated Lupus, Dermatomyositis and Scleroderma. The connective tissue change is wide-spread, but principle sites effected are joints in rheumatic diseases, blood vessels in Polyarteritis Nodosa and Disseminated Lupus, skin and fascial ...

متن کامل

Thrombosis in systemic lupus erythematosus: striking association with the presence of circulating lupus anticoagulant.

The lupus anticoagulant was found in the plasma of 31 of 60 patients with systemic lupus erythematosus and other connective tissue disorders (mixed connective tissue disease, systemic vasculitis, polyarteritis nodosa, primary sicca syndrome, discoid lupus, Behcet's syndrome, and systemic sclerosis). Strong associations were found with biological false positive seroreaction for syphilis and thro...

متن کامل

Polyarteritis nodosa with new bone formation.

Polyarteritis nodosa was first described as a clinico-pathological entity by Kussmaul and Maier ( 1866), who called it periarteritis nodosa. Ferrari (1903) first called the disease polyarteritis nodosa, a name that describes the pathology more accurately. The disease may be grouped with the collagen diseases-desseminated lupus erythematosis, scleroderma, rheumatoid arthritis and others. It is c...

متن کامل

Necrotizing Polyarteritis Nodosa-like Vasculitis in a Child with Systemic Lupus Erythematosus.

A 10-year-old child presented with prolonged fever, lymphadenopathy, weight loss, oral ulcers, alopecia and parotitis. She later developed arterial thrombosis, poly-serositis, nephritis, myocarditis, sacro-ilitis, autoimmune hemolytic anemia and refractory thrombocytopenia. Though anti-dsDNA was negative, she was diagnosed to have systemic lupus erythematosus (SLE). Terminally, she had pulmonar...

متن کامل

Lupus erythematosus cells in systemic sclerosis.

The lupus erythematosus cell (L.E. cell) phenomenon is usually regarded, if properly interpreted, as being almost specific for systemic lupus erythematosus (Wilkinson and Sacker, 1957). On the other hand, too rigid an outlook may lead to diagnostic errors or retard progress in the understanding of other diseases. Careful repeated examination of the blood of patients with classical rheumatoid ar...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Clinical and experimental rheumatology

دوره 19 6  شماره 

صفحات  -

تاریخ انتشار 2001