Rosai Dorfman disease: appearances can be deceptive
نویسندگان
چکیده
منابع مشابه
Rosai-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...
متن کاملIntracranial Rosai-Dorfman Disease
Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of other sites. It is a rare and idiopathic histoproliferation disorder characterized by painless lymphadenopathy. We report a case of 43-year-old m...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2012
ISSN: 1757-790X
DOI: 10.1136/bcr-2012-006723