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¼Û°ú¿ø±âÁ¾¾ç - 1¿¹ º¸°í - Pineal Anlage Tumor - A case report -

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ÃÖÁ¾¼ø, ½ÅÇüÁø, ¼­¿¬¸²,
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ÃÖÁ¾¼ø ( Choi Jong-Sun ) 
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼­¿ïº´¿ø Áø´Üº´¸®°ú

½ÅÇüÁø ( Shin Hyung-Jin ) 
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼­¿ïº´¿ø ½Å°æ¿Ü°úÇб³½Ç
¼­¿¬¸² ( Suh Yeon-Lim ) 
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼­¿ïº´¿ø Áø´Üº´¸®°ú

Abstract


The term "pineal anlage tumor" has been recently proposed and few cases have been reported. We report the first Korean case of pineal anlage tumor in a 6-year-old girl who complained of headache and vomiting for 2 months. Brain MRI revealed a well defined, lobulated, calcifying mass in the pineal region. Tumor was totally removed. Pathological examination revealed a primitive pineal parenchymal tumor with melanotic epithelial component that was similar to histologic findings of melanotic neuroectodermal tumor of infancy, so-called retinal anlage tumor and of the developing pineal gland. The tumor was composed mostly of small, undifferentiated cells, Flexner-Wintersteiner rosettes, and ganglionic differentiation. The tumor also contained the cartilage and skeletal muscle cells.

Å°¿öµå

Pineal anlage tumor;Pineoblastoma;Melanotic neuroectodermal differentiation

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