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¼±Ãµ¼º µÎ°³³» Áö¹æÁ¾ 2·Ê Two Cases of Congenital Intracranial Lipoma

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ÀÌÇý·É ( Yi Hye-Ryoung ) 
Àü³²´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç

¼ÛÀº¼Û ( Song Eun-Song ) 
Àü³²´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
ÃÖ¿µ·û ( Choi Young-Youn ) 
Àü³²´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
¼Ûź¹ ( Song Tae-Bok ) 
Àü³²´ëÇб³ ÀÇ°ú´ëÇÐ »êºÎÀΰúÇб³½Ç
±è¹ÌÁ¤ ( Kim Mi-Jung ) 
Àü³²´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
Á¤½Å ( Jung Shin ) 
Àü³²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ¿Ü°úÇб³½Ç

Abstract


Intracranial lipoma is a rare tumor. It is considered as congenital malformation, caused by poor differentiation and abnormal persistence of the primitive meninges. More frequently intracranial lipomas are central and located in the midline especially in corpus callosum. We report the two cases of intracranial lipoma, one case was detected in cerebellum by antenatal sonography and the other one was detected in right temporal cistern by cranial sonography during the postnatal follow-up. (J Korean Soc Neonatol 2006;13:160-164)

Å°¿öµå

Congenital;Intracranial lipoma;Cerebellum

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KCI
KoreaMed
KAMS