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Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a congenital disorder of the lung similar to bronchopulmonary sequestration. In CPAM, usually an entire lobe of lung is replaced by a non-working cystic piece of abnormal lung tissue.
CCAM codes are structured in a tree whose top-level comprises 19 chapters, organized mainly by large anatomical structure or function: 01. central nervous system, device and independent; 02. eye and notes; 03. ear; 04. circulatory; 05. immune system and hematopoietic; 06. respiratory; 07. digestive; 08. urinary and genital
There is still much debate to whether pulmonary sequestration is a congenital problem or acquired through recurrent pulmonary infection. It is widely believed that extralobar pulmonary sequestrations are a result of prenatal pulmonary malformation while intralobar pulmonary sequestrations can develop due to recurrent pulmonary infections in adolescents and young adults.
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Congenital cystic adenomatoid malformation, now known as congenital pulmonary airway malformation (CPAM) cCam, a camera capture program that runs on Nokia S60 phones Center for research on Children, Adolescents, and the Media at the University of Amsterdam , the Netherlands
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