Cystic adenomatoid malformation of fetus
Authors:
K. Bihariová 1; D. Kobidová 1; T. Bielik 2; P. Molitoris 1
Authors‘ workplace:
Gynekologicko-pôrodnícke oddelenie, NsP Zvolen, a. s., primár MUDr. P. Molitoris
1; Gynekologicko-pôrodnícka klinika, Fakultná nemocnica s poliklinikou F. D. Roosevelta, Banská Bystrica, prednosta doc. MUDr. T. Bielik, PhD.
2
Published in:
Ceska Gynekol 2017; 82(6): 474-477
Overview
Objective:
Presentation of prenataly diagnosed fetus with congenital cystic adenomatoid malformation (CCAM). Summary of clinical and histological findings in fetuses with CCAM, in utero ultrasound diagnosis, prognosis, in utero dispensarisation, timing of delivery and postanatal management.
Design:
Case report.
Settings:
Nemocnica s poliklinikou, Zvolen, a.s., gynekologicko-pôrodnícke oddelenie.
Case report:
In this article we would like to introduce the case report of fetus suffering from CCAM.
Conclusions:
Congenital cystic adenomatoid malformation is a rare congenital disorder. The clinical and histological findings can vary. The diagnose can be made in prenatal period due to the availability of prenatal ultrasound examination.
Keywords:
congenital cystic adenomatoid malformation of lung, prenatal ultrasound diagnosis, polyhydramnion
Sources
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Paediatric gynaecology Gynaecology and obstetrics Reproduction medicineArticle was published in
Czech Gynaecology
2017 Issue 6
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