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   Rothmund-Thomson Syndrome with Malignant Fibrous Histiocytoma: Report of a Case and Review of Literature  
   
نویسنده Aziz Jalali MirHadi ,Tabaie Mehdi
منبع iranian journal of dermatology - 2010 - دوره : 13 - شماره : 1 - صفحه:27 -29
چکیده    Rothmund–thomson syndrome is a rare autosomal recessive genodermatosis characterized by early onset of poikiloderma and several other cutaneous and organ involvements. we are going to report a 14-year-old girl who has been diagnosed with rothmund– thomson syndrome since she was 3 years old and has been suffering from pain and swelling of the right elbow and forearm for about 6 months. there are few previous reports on rothmund–thomson syndrome associated with malignant fibrous histiocytoma. we decided to report this case as another supporting document for this association.
کلیدواژه poikiloderma ,malignant fibrous histocytoma ,Rothmund–Thomson syndrome
آدرس iran university of medical sciences, Department of Dermatology, ایران, iran university of medical sciences, Department of Dermatology, ایران
پست الکترونیکی sabaderm@ yahoo.com
 
     
   
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