HIGHLIGHTS
SUMMARY
Congenital cystic adenomatoid malformation (CCAM) is an unusual form of cystic disease of the lungs, also known as congenital pulmonary adenomatoid malformation (CPAM). When following the Stocker classification system, CCAM may be subdivided into three types, based on gross and microscopic criteria: type I is usually associated with a good prognosis and includes multiple large cysts (>2 cm in diameter) or a single large cyst, surrounded by numerous smaller cysts. Type II represents over 40% of all CCAM cases, and is associated with multiple small cysts ( and amp;lt;1 cm in diameter), lined . . .
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