Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosum.
Marco Pizzi, Matteo Fassan, Kathrin Ludwig, Matteo Cassina, Maria Teresa Gervasi, Roberto Salmaso
Department of Medical Diagnostic Sciences & Special Therapies, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy.
Fetal and pediatric pathology 2012 JunCongenital pulmonary airway malformations (CPAM) are a family of hamartomatous disorders due to the uncontrolled overgrowth of the terminal bronchioles. Congenital pulmonary airway malformations can co-exist with cardiovascular and/or urogenital malformations, but their association with thoracopulmonary malformations is extremely rare. We report the first case of CPAM type I, co-existing with tracheo-esophageal fistula and corpus callosum agenesis.
Citation
Marco Pizzi, Matteo Fassan, Kathrin Ludwig, Matteo Cassina, Maria Teresa Gervasi, Roberto Salmaso. Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosum. Fetal and pediatric pathology. 2012 Jun;31(3):169-75
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PMID: 22414029
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