A case of congenital cystic adenomatoid malformation infected with Mycobacterium avium-intracellulare complex

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Abstract

We present a case of congenital cystic adenomatoid malformation (CCAM) in a 25-year-old male who was presented with chronic cough. Chest radiography revealed an abnormal mass-like shadow in the right lower pulmonary zone. A contrast enhanced computed tomography showed an 11 cm solid, cystic mixed mass on the right lower lobe. A right lower lobectomy was performed by video-assisted thoracoscopic surgery without complications. The gross specimen showed a massive cavitation with multiloculated cysts of varying size, consistent with CCAM, along with noticeable granulomatous inflammation. Non-tuberculosis mycobacteria were isolated from a bronchial wash specimen, and the resected tissue homogenates were positive for Mycobacterium avium-intracellulare complex by polymerase chain reaction. Copyright©2013. The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved.

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Kim, Y. J., Kim, D. Y., Seo, J. W., Lee, S. A., Hwang, J. J., Kim, H. J., & Lee, K. Y. (2013). A case of congenital cystic adenomatoid malformation infected with Mycobacterium avium-intracellulare complex. Tuberculosis and Respiratory Diseases, 74(1), 28–31. https://doi.org/10.4046/trd.2013.74.1.28

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