![]() It is generally accepted that the various types of CCAMs originate at different levels of the tracheobronchial tree. Hum Pathol 1999 Jun 30(6):618-25 Abstract quote Congenital cystic adenomatoid malformation of the lung (CCAM) is a rare congenital lesion whose pathogenesis is not well defined. We studied the bronchial and vascular trees by mapping bronchi, pulmonary blood vessels, systemic blood vessels, the size and configuration of cysts, and associated scarring. Design.-We studied 10 consecutive cases of surgically resected cystic lung disease in children. Objective.-To clarify the identity of congenital cystic adenomatoid malformation in relation to other cystic diseases. Arch Pathol Lab Med 2002 Aug 126(8):934-940 Abstract quote Context.-Congenital cystic adenomatoid malformation, intralobar sequestration, extralobar sequestration, bronchopulmonary foregut malformation, bronchial atresia, and lobar emphysema generally are treated as separate entities, but there are commonalities among them. Kobe Children's Hospital of Hyogo Prefecture, Kobe, Japan, the Department of Pathology, Massachusetts General Hospital, Boston, Mass, Kobe Operation Center, International Center for Diagnostic Pathology, Kobe, Japan, and Kobe City General Hospital, Kobe, Japan (Dr Imai) and the Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Mass (Dr Mark).
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