Congenital cystic adenomatoid malformation with prenatal diagnosis: case report

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KALAY S., OZTEKIN O., TEZEL G., Basaran E., KERNAK A., Akcakus M., ...Daha Fazla

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.47, sa.4, ss.294-297, 2012 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 47 Sayı: 4
  • Basım Tarihi: 2012
  • Doi Numarası: 10.4274/tpa.293
  • Dergi Adı: TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.294-297
  • Anahtar Kelimeler: Congenital cystic adenomatoid malformation, newborn, LUNG, MANAGEMENT
  • Akdeniz Üniversitesi Adresli: Evet

Özet

Congenital cystic adenomatoid malformation is a hamartomatous malformation accepted as an embryonic differentiation anomaly characterized by replacement of normal lung parenchyma by cysts of various sizes and numbers. The primigravid presented on her 24th week with the ultrasound findings of a fetus with unilateral cyts in left lung. Thoracoamniotic shunting was inserted at a mean gestational age of 24. Patient was born due to premature rupture of membranes and preterm delivery at a mean gestational age of 25. We present a case of congenital cystic adenomatoid malformation type I in a newborn who died in twelve hours after birth and discuss about pre- and postnatal diagnostic and therapeutic possibilities. (Turk Arch Ped 2012; 47: 294-7)