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Adenocarcinoma Arising in Type 1 Congenital Cystic Adenomatoid Malformation: A Case Report and Review of the Literature

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À¯Áø¿µ, À̼±¹Ì, Á¤ÁöÇÑ, ¾È¸íÀÓ, Á¶´ö°ï, °­¼®Áø, À̱³¿µ,
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À¯Áø¿µ ( Yoo Jin-Young ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

À̼±¹Ì ( Lee Sun-Mi ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
Á¤ÁöÇÑ ( Jung Ji-Han ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
¾È¸íÀÓ ( Ahn Myeong-Im ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ ¼ººó¼¾Æ®º´¿ø ¿µ»óÀÇÇаú
Á¶´ö°ï ( Cho Deog-Gon ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ ¼ººó¼¾Æ®º´¿ø ÈäºÎ¿Ü°ú
°­¼®Áø ( Kang Seok-Jin ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
À̱³¿µ ( Lee Kyo-Young ) 
°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

Abstract


Malignancies in congenital cystic adenomatoid malformations (CCAMs) of the lung are rare. We report a 41-year-old male patient with a pulmonary cystic lesion suspicious for CCAM, unrecognized until the patient was 40 years of age, and which subsequently became more consolidated during the interval between initial presentation and surgery. Microscopic examination of the resected specimen revealed features of type 1 CCAM with a mucinous adenocarcinoma, metastatic to the mediastinal lymph nodes. This case illustrates the importance of prompt surgical resection for all suspected CCAMs, especially those discovered in adulthood.

Å°¿öµå

Congenital cystic adenomatoid malformation; Adenocarcinoma

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