جلد 9، شماره 32 - ( 12-1381 )
جلد 9 شماره 32 صفحات 642-637 |
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Owlia M, Haghighi A, Javadzadeh A. SCLERODERMA-LIKE SYNDROM (WERNER’S SYNDROM) “A RARE CASE REPORT”. RJMS 2003; 9 (32) :637-642
URL: http://rjms.iums.ac.ir/article-1-1678-fa.html
URL: http://rjms.iums.ac.ir/article-1-1678-fa.html
اولیاء محمدباقر، حقیقی انوشه، جوادزاده علی. سندرم شبه اسکلرودرمی معرفی یک بیمار نادر (سندرم ورنر). مجله علوم پزشکی رازی. 1381; 9 (32) :637-642
چکیده: (7211 مشاهده)
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, hyperpigmentation and susceptibility to malignant neoplasms. We describe a case of Werner’s syndrome who presented with chronic leg ulcer and was misdiagnosed as systemic sclerosis for many years. We stopped unnecessary treatments and chronic leg ulcer was biopsied to rule out of skin cancer and managed locally by antibiotics and daily care.
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