نتایج جستجو برای: paraproteinemia scleromyxedema systemic sclerosis
تعداد نتایج: 231334 فیلتر نتایج به سال:
Necrobiotic xanthogranuloma is a rare, idiopathic, and chronic systemic granulomatous disorder that is usually associated with paraproteinemia of the immunoglobulin (Ig)G kappa (κ) type. It is clinically characterized by yellowish red-to-brown indurated often ulcerating nodules or plaques that usually involve the periorbital regions of the elderly. We report an atypical case of NXG affecting on...
objective: systemic sclerosis (ss) is a chronic autoimmune disease of connective tissue, which involves skin and internal organs, and results in collagen deposition and fibroblasts activation. studies have reported a higher risk of malignancy in patients with progressive systemic sclerosis (pss).the aim of this study is to report a case of tongue squamous cell carcinoma (scc) in a patient with ...
aim : we described two case reports of aih/ssc overlap syndrome and reviewed literatures regarding this issue. background : aih is a chronic hepatitis of unknown aetiology characterized by continuing hepatocellular necrosis and inflammation. aih overlap syndromes have been reported with other autoimmune diseases. patients and methods : according to the classification criteria for ssc, we cond...
Scleroderma-like syndromes are a group of disorders that mimic systemic sclerosis. Werner’s syndrome is a genetically inherited syndrome that can be misdiagnosed as systemic scleroderomia. The syndrome is charachterized by sclerosis or stiffening of the skin, progeris, bilatera l juvenile cataract, endocrinopathies, premature coronary artery disease, alopecia, nail plate changes, hyperpigmentat...
ABSTRACT Systemic sclerosis is a disease with skin tightness. Besides of skin involvement, there may be involvement of different organs. Systemic sclerosis may be diffuse or limited, but in both of them Raynoud’s phenomen is common. This phenomen is due to vasoconstriction and vascular insufficiency and is a phenomen that makes problem for the patient and does not have any efficient treatment....
A 63-year-old woman suffering from progressive systemic sclerosis for about 20 years disclosed symptoms of liver disease within the last three years. Diagnosis of biliary cirrhosis was established on the basis of clinical picture, pathological examination of the hepatic tissue sample, immunological tests, and x-ray studies. Association of systemic sclerosis with primary biliary cirrhosis is...
INTRODUCTION Scleromyxedema is a rare, chronic and progressive disorder of unknown origin characterized by a generalized papular eruption and sclerodermoid induration, with histopathologic features of mucin deposition and fibroblast proliferation. The disease is usually associated with a monoclonal gammopathy. However, only a few cases associated with neoplasms have been reported. We report a c...
Systemic sclerosis (SSc) is characterized by vascular abnormalities, fi brosis, infl ammatory changes, and late stage tissue atrophy of the skin and several internal organs. In scleroderma-like disorders the distribution/characteristics of skin involvement is different. The skin involvement of the acral regions including digits is usually missing. Lack of Raynaud’s phenomenon, and scleroderma-s...
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