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Abstract

15°³¿ù ³²¾Æ¿¡¼­ °üÂûµÈ °£ÀåÀÇ ³¶¼º °£¿±¼º °ú¿ÀÁ¾ÀÇ 1¿¹¸¦ º¸°íÇÏ¿´´Ù. ȯÀÚ´Â »ýÈÄ 11
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´Ù. Å©±â´Â 16¡¿15¡¿8§¯¿´´Ù. Á¾±«´Â À°¾ÈÀûÀ¸·Î ȸ¹é»öÀ¸·Î ¸¹Àº ³¶¼º±¸Á¶¸¦ °¡Áö´Â Å« Á¾
±«¿´À¸¸ç ÁÖÀ§¿ÍÀÇ °æ°è´Â ¸íÈ®ÇÏ¿´´Ù. Çö¹Ì°æÀûÀ¸·Î °£¼¼Æ÷ÀÇ ¼¶µé°ú ´õºÒ¾î ´ã°üÀÇ Áõ½Ä
ÀÌ ÀÖ¾ú°í, ÀÌ¿ÍÇÔ²² Á¡¾×¼º Á¶Á÷ Áï È°µ¿¼º ¼¶À¯ ¸ð¼¼Æ÷Áõ½Ä°ú ºÎÁ¾ ±×¸®°í ¾à°£ÀÇ ¸Æ°üÁ¶
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#ÃÊ·Ï#
A typical example of congenital cystic mesenchymal hamartoma of the liver is
reported in a 15 months old boy who presented with abdominal distension at eleven
months of age.
The tumor was in the left lobe and was a large circumscribed nodular mass
measuring 16cm in maximum dimensioin. Numerous cysts were seen on the cut surface
that were interconnected to form a large gray white mass which was well demarcated
from the surrounding liver. Microscopically, the tumor was characterized by both
epithelial and mesenchymal proliferation, epithelial being bile ducts and hepatocytes.

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