Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature

Turan O., HIRFANOĞLU İ. M., BEKEN S., Biri A., Efeturk T., Atalay Y.

TURKISH JOURNAL OF PEDIATRICS, vol.53, no.3, pp.337-341, 2011 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 53 Issue: 3
  • Publication Date: 2011
  • Journal Name: TURKISH JOURNAL OF PEDIATRICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.337-341
  • Keywords: congenital cystic adenomatoid malformation, trisomy
  • Acibadem Mehmet Ali Aydinlar University Affiliated: No

Abstract

Congenital cystic adenomatoid malformation (CCAM) is a rare bronchopulmonary malformation characterized by loss of the normal pulmonary tissue. CCAM may be frequently associated with cardiac and renal anomalies. Rarely, CCAM may be seen with chromosome abnormalities. This is the first reported neonatal case of prenatally detected CCAM and postnatally diagnosed trisomy 13.