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KMID : 0364019930260040320
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Korean Journal of Thoracic and Cardiovascular Surgery
1993 Volume.26 No. 4 p.320 ~ p.324
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Surgical Treatment of Congenital Cystic Adenomatoid Malformation -1 Case Report-
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Abstract
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Congenital cystic adenomatoid malformation(CCAM) of the lung is extremely rare. The patient was 10 year old female and had no specipic signs and symptoms except right lower chest pain for 5 days ago before admission. On simple chest X-ray and
thoracic
CT scan, about 9*8*8cm sized, heterogenous marginally enhanced multiseparated hypodence lesion with air fluid level and gas bubbles in posterior pleural space of right lower chest were found. The culture result of needle aspiration of cavity was
apergillus flavus.
Right lower lobectomy was carried out and the result of biopsy was congenital cystic adenomatoid malformation. (Korean J Thoracic Cardiovas Surg 1994; 27:320-324)
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