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Isolated Intracranial Rosai-Dorfman Disease -A Case Report-
¹ÚÁø±Ô, Á¶¹Ì¿¬, º¯Áø¼ö, ¹Ú±¤ÇÏ,
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¹ÚÁø±Ô ( Park Jin-Kyu )
¿¬¼¼´ëÇб³ ¿øÁÖÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
Á¶¹Ì¿¬ ( Cho Mee-Yon )
¿¬¼¼´ëÇб³ ¿øÁÖÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
º¯Áø¼ö ( Pyen Jhin-Soo )
¿¬¼¼´ëÇб³ ¿øÁÖÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
¹Ú±¤ÇÏ ( Park Kwang-Hwa )
¿¬¼¼´ëÇб³ ¿øÁÖÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
KMID : 0357920040380060430
Abstract
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.
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Rosai Dorfman disease;Meninges;Intracranial
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