Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
نویسندگان
چکیده
Dermatomyositis (DM) is an autoimmune disease that is characterized by involvement of proximal musculature and skin. We report a 52-year-old woman with a 6-year history of dermatomyositis sine myositis, who developed lower extremity edema and proteinuria. Pathological examination of renal biopsy showed membranoproliferative glomerulonephritis. She received steroid, cyclophosphamide, and mycophenolate mofetil. Over the 9 to 10 months after the beginning of treatment, the proteinuria was improved.
منابع مشابه
Superimposed Polymyositis in a Patient with Myeloperoxidase-Related Crescentic Glomerulonephritis
Renal involvement especially glomerulonephropathy in polymyositis or dermatomyositis is considered rare. Crescentic glomerulonephritis is even more so. Herein, we report a patient who was diagnosed with concurrent polymyositis and myeloperoxidase-related crescentic glomerulonephritis. We discuss the association between polymyositis or dermatomyositis and renal involvement, glomerulonephropathy,...
متن کاملPositive for Anti-Jo-1 and Anti-Cyclic Citrullinated Peptide Antibodies Myositis Sine Destructive Arthropathy Associated with Dermatomyositis
3. Information on permissions/orders of reprints in rheumatology and related fields. Silverman featuring research articles on clinical subjects from scientists working is a monthly international serial edited by Earl D.
متن کاملJuvenile dermatomyositis (JDM) sine myositis
Methods/case 6 y/o girl from Kazakhstan presenting with discrete heliotrope of upper eyelids, erythema of the chest and extensor surfaces of extremities, Gottron’s papules as well as scarred piecemeal necrosis on 1 finger and 2 toes. Close examination revealed nailfold tortuositas. Muscle strength was 5/5, CMAS 48/51. Inflammatory parameters were not elevated, transaminases, CK and aldolase in ...
متن کاملSuperimposed Segmental Manifestation of Juvenile Amyopathic Dermatomyositis in a 9-year-old Boy
Dermatomyositis is a well-known autoimmune disorder. On the other hand, juvenile amyopathic dermatomyositis (JADM) occurs rather rarely. Here, we report an unusual case in a 9-year-old Turkish boy showing a unilateral linear inflammatory skin lesion that was followed, after 16 months, by the appearance of bilateral disseminated features JADM.
متن کاملAn elusive case of dermatomyositis.
Dermatomyositis is an inflammatory myopathy of unknown aetiology. Muscle involvement may eventuate later in the disease course in some patients, who may present with typical skin disease without clinical signs of myopathy and are referred to as dermatomyositis sine myositis. A 48 year old female presented with intermittent urticaria like rashes, diffuse asymmetrical swelling of proximal limbs, ...
متن کاملذخیره 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 ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
دوره 2012 شماره
صفحات -
تاریخ انتشار 2012