단독성 두개내 Rosai-Dorfman병 -1예 보고
Rosai-Dorfman disease (RDD) is an idiopathic histioproliferative disorder of the lymph nodes and extranodal sites. Central nervous system involvement is extremely rare. Intracranial RDD, especially the isolated form, resembles meninigioma both clinically and radiologically. Here, we report a case of...
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Published in | Journal of pathology and translational medicine pp. 430 - 433 |
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Main Authors | , , , |
Format | Journal Article |
Language | Korean |
Published |
대한병리학회
01.12.2004
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Subjects | |
Online Access | Get full text |
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Summary: | Rosai-Dorfman disease (RDD) is an idiopathic histioproliferative disorder of the lymph nodes and extranodal sites. Central nervous system involvement is extremely rare. Intracranial RDD, especially the isolated form, resembles meninigioma both clinically and radiologically. Here, we report a case of isolated, intracranial, dura-based RDD. The patient presented with headache and dizziness with no evidence of lymphadenopathy. Histologically, the lesion consisted of large histiocytes with emperipolesis and lymphoplasma cell infiltrates with a fibrotic background. We discuss the differential diagnosis of this lesion. To our knowledge, this is the first reported Korean case of intracranial RDD. KCI Citation Count: 0 |
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Bibliography: | http://kmbase.medric.or.kr/Main.aspx?d=KMBASE&m=VIEW&i=0357920040380060430 G704-000333.2004.38.6.013 |
ISSN: | 2383-7837 2383-7845 |