Rothmund-Thomson Syndrome with Malignant Fibrous Histiocytoma: Report of a Case and Review of Literature
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نویسنده
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Aziz Jalali MirHadi ,Tabaie Mehdi
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منبع
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iranian journal of dermatology - 2010 - دوره : 13 - شماره : 1 - صفحه:27 -29
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چکیده
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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.
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کلیدواژه
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poikiloderma ,malignant fibrous histocytoma ,Rothmund–Thomson syndrome
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آدرس
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iran university of medical sciences, Department of Dermatology, ایران, iran university of medical sciences, Department of Dermatology, ایران
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پست الکترونیکی
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sabaderm@ yahoo.com
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