¼Û°ú¿ø±âÁ¾¾ç - 1¿¹ º¸°í -
Pineal Anlage Tumor - A case report -
ÃÖÁ¾¼ø, ½ÅÇüÁø, ¼¿¬¸²,
¼Ò¼Ó »ó¼¼Á¤º¸
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
KMID : 0357920000340121029
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
¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸
µîÀçÀú³Î Á¤º¸