اولياء, محمدباقر and حقيقی, انوشه and جوادزاده, علی (2003) سندرم شبه اسکلرودرمی معرفی يک بيمار نادر (سندرم ورنر). مجله علوم پزشکی رازی, 9 (32). pp. 637-642. ISSN 2228-7051
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Abstract
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
Item Type: | Article |
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Uncontrolled Keywords: | سندرم ورنر، پیری زودرسسندرم ،شبه اسکلرودرمی، اسکلروز سیستمیک، |
Subjects: | R Medicine > R Medicine (General) |
Divisions: | Other Journal > Razi Journal of Medical Sciences |
Depositing User: | Touba Derakhshande |
Date Deposited: | 14 Jan 2015 09:53 |
Last Modified: | 14 Jan 2015 09:53 |
URI: | http://eprints.bpums.ac.ir/id/eprint/2593 |
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