Æó¿¡ ¹ß»ýÇÑ ³¶¼º ¸²ÇÁ°üÁ¾
Intrapulmonary Cystic Lymphangioma
ÁöÁ¦±Ù, Àü¹Ì¿µ,
¼Ò¼Ó »ó¼¼Á¤º¸
ÁöÁ¦±Ù ( )
¼¿ï´ëÇб³º´¿ø ¼Ò¾Æº´¸®°ú
Àü¹Ì¿µ ( )
ºÎ»ê¹éº´¿ø Çغκ´¸®°ú
KMID : 0357919970310050492
Abstract
Æó¿¡¼ÀÇ ¸²ÇÁ°üÁ¾Àº ¾ÆÁÖ µå¹°¸ç ƯÈ÷ ´Ü¹æÇüÀÇ Å« ³¶¼º Á¾±«·Î ³ªÅ¸³ª´Â °æ¿ì´Â ÀÌÀü±î
ÁöÀÇ ¹®Çå¿¡ º¸°íµÈ ¿¹°¡ ¾ø¾ú´Ù. ÀúÀÚµéÀº ÃÖ±Ù¿¡ ¿µ¾Æ¿¡ ¹ß»ýÇÑ Ã¼ÀÇ °í¸³¼º ³¶¼º ¸²ÇÁ°ü
Á¾ 1¿¹¸¦ °æÇèÇÏ¿´±â¿¡ º¸°íÇÏ´Â ¹ÙÀÌ´Ù.
#ÃÊ·Ï#
Solitary intrapulmonary cystic lymphangioma in newborn or infant is an extremely
rare disease. We describe a case of solitary intrapulmonary cystic lymphangioma in a
4-month-old boy with dyspnea and tachypnea. It was in the left lower lobe and type 1
congenital cystic adenomatoid malformation was suspected radiologically. The rejected
cyst was unilocular with a thin wall, and was 9.5cm in size. Histologically, the cyst was
lined by flattened endothelial cells supported by a minimal fibrous stroma.
Å°¿öµå
Cystic lymphangioma; Solitary; Infant; Lung;
¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸
µîÀçÀú³Î Á¤º¸