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Cutaneous Rosai-Dorfman disease: A separate clinical entity
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نویسنده
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hinojosa tiffany ,ramos elmira ,lewis daniel j. ,angel laurent del ,vangipuram ramya ,peranteau andrew j. ,tyring stephen k.
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منبع
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journal of dermatology and dermatologic surgery - 2017 - دوره : 21 - شماره : 2 - صفحه:107 -109
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چکیده
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Rosai-dorfman disease is a benign, self-limited non-langerhans cell histiocytosis of unknown etiology. its most common clinical feature is extraordinary massive painless cervical lymphadenopathy. this entity may be limited to the lymph nodes; however, more than 40% of patients have extranodal involvement, with the skin being the most frequently affected site. cutaneous disease without the presence of lymphadenopathy is extremely rare but has been reported. we report the intriguing case of exclusively cutaneous rosai-dorfman disease in an 80-year-old african-american woman.
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کلیدواژه
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Rosai-Dorfman disease; Histiocytosis; Lymphadenopathy; Dermatopathology
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آدرس
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university of monterrey, faculty of medicine, Mexico, universidad auto´noma de tamaulipas, Mexico, baylor college of medicine, school of medicine, USA. university of texas, md anderson cancer center, department of dermatology, USA, universidad auto´noma de tamaulipas, Mexico, center for clinical studies, USA, center for clinical studies, USA, center for clinical studies, USA. university of texas, health science center at houston, department of dermatology, USA
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Authors
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