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Fetal and Pediatric Pathology

Volume 31, 2012 - Issue 3
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Research Article

Congenital Pulmonary Airway Malformation (CPAM) [Congenital Cystic Adenomatoid Malformation] Associated with Tracheoesophageal Fistula and Agensesis of the Corpus Callosum

Marco Pizzi Department of Medical Diagnostic Sciences & Special Therapies, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy
, MD,
Matteo Fassan Department of Medical Diagnostic Sciences & Special Therapies, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy
, MD,
Kathrin Ludwig Department of Medical Diagnostic Sciences & Special Therapies, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy
, MD,
Matteo Cassina Department of Pediatrics, Clinical Genetics Unit, University Hospital, Padua, Italy
, MD,
Maria Teresa Gervasi Obstetrics and Gynecology Unit, Padua Teaching Hospital & University of Padua, Padua, Italy
, MD &
Roberto Salmaso Department of Medical Diagnostic Sciences & Special Therapies, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, ItalyCorrespondenceroberto.sanita.padova.it
, MD
Pages 169-175
Published online: 13 Mar 2012
 
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Abstract

Congenital 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.

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