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


Turan O., Hirfanoglu I. M. , Beken S. , Biri A., Efeturk T., Atalay Y.

TURKISH JOURNAL OF PEDIATRICS, cilt.53, ss.337-341, 2011 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 53 Konu: 3
  • Basım Tarihi: 2011
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Sayfa Sayısı: ss.337-341

Özet

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.