Rosai-Dorfman disease successfully treated with thalidomide
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چکیده
منابع مشابه
Rosai-Dorfman disease successfully treated with thalidomide
ESR: erythrocyte sedimentation rate INTRODUCTION Rosai-Dorfman disease, also called sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic condition of unknown etiology first described in 1969. Primary cutaneous manifestation without systemic involvement of Rosai-Dorfman disease is even more uncommon. Here we present a case of primary cutaneous manifestation of Rosai-Dorfman di...
متن کاملRosai-Dorfman Disease.
A young male presented with recurrent neck swellings with initial leucocyte count of 16800/mm3, with non-caseating glands on ultrasonography neck. FNAC showed mixed cellularity with histiocytic and marked lymphophagocytosis as seen in Rosai Dorfman Disease. Immunohistochemistry demonstrated CD 25, Ki 67 and CD 68 in histiocytes. Her responded to supportive treatment alone.
متن کاملIntrathoracic Rosai-Dorfman Disease
231 Received March 23, 2012; revision accepted for publication June 21, 2012. doi: 10.1620/tjem.227.231 Correspondence: Shingo Noguchi, M.D., Department of Respiratory Medicine, University of Occupational and Environmental Health, Iseigaoka, Yahatanishiku, Kitakyushu city, Fukuoka 807-8555, Japan. e-mail: [email protected] Intrathoracic Rosai-Dorfman Disease with Spontaneous Remission: A ...
متن کاملIntracranial ROSAI-DORFMAN Disease
Rosai-Dorfman disease is a benign lymphohistiocytosis that often involve lymph nodes and present as massive lymphadenopathy with sinus histiocytosis. The disease is rarely associated with intracranial involvement. Herein, we report a 33-years-old man with recent onset of unconsciousness. According to his past medical history, he was suffering from frontal headache, ataxia and dizziness with no ...
متن کاملCutaneous Rosai-Dorfman disease.
Rosai-Dorfman disease (RDD) is a rare benign proliferative disorder of histiocytes in the lymph nodes with or without extranodal involvement. RDD limited to the skin without nodal involvement, known as cutaneous Rosai-Dorfman disease, is very rare. We describe a 34-year-old female with RDD of the skin over the chest. A large nodule with satellite lesions was excised for histopathological examin...
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ژورنال
عنوان ژورنال: JAAD Case Reports
سال: 2016
ISSN: 2352-5126
DOI: 10.1016/j.jdcr.2016.08.006