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Abstract

Æó ¹«¹ßÀ°Áõ(pulmonary agenesis)Àº Æó½ÇÁú, Ç÷°ü±¸Á¶ ¹× ±â°üÁö ºÐÁöºÎ ÀÌÇÏ°¡ Çü¼ºµÇÁö
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µ¿¹ÝÇÑ´Ù. 1929³â PaulÀÌ Ã³À½À¸·Î ½ÄµµÆó¼âÁõ°ú ±â°ü½Äµµ´©°øÀÌ µ¿¹ÝµÈ Æó ¹«¹ßÀ°ÁõÀ» º¸
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ÀúÀÚµéÀº ÀӽŠ33ÁÖ¿¡ Á¦¿ÕÀý°³ÈÄ 24½Ã°£ ³»¿¡ »ç¸ÁÇÑ ºÎ°Ë ¿¹¿¡¼­ ½ÄµµÆä¼âÁõ°ú ±â°ü½Ä
µµ´©°ø µîÀÇ ´Ù¸¥ ±âÇüÀ» µ¿¹ÝÇÑ Æó ¹«¹ßÀ°ÁõÀÇ ¸Å¿ì º¸±â µå¹® ±âÇüÀ» °æÇèÇÏ¿´±â¿¡ °£´Ü
ÇÑ ¹®Çå°íÂû°ú ÇÔ²² º¸°íÇÏ°íÀÚ ÇÑ´Ù.
#ÃÊ·Ï#
Pulmonary agenesis is a very rare anomaly. It is defined as total absence of the
pulmonary parenchyma, vascular structures, and bronchi beyond the carina.
We experienced a case of right pulmonary agenesis in association with other
congenital defects who died at 1 day of age. The other defects included: esophageal
atresia, tracheoesophageal fistula, cardiac malformation, anal atresia and a malformed left
thumb. The cardiac malformations were a type of Pentalogy of Fallot, composed of right
ventricular hypertrophy, ventricular septal defect, an overiding of aorta, pulmonary
atresia, and an atrial septal defect. Hand roentgenograms of the malformed left thumb
showed an unarticulated metacarpopharyngeal joint. This unique combination of
anomalies is extremely rare.

Å°¿öµå

Pulmonary agenesis; Esophageal atresia; Tracheoesophageal fistula; Pentalogy of Fallot;

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