Prenatal Diagnosis of Fetal Trisomy 5 Mosaicism with Congenital Pulmonary Airway Malformation Type 3: A Case Report

Author(s):  
Maria Paola Bonasoni ◽  
Giuseppina Comitini ◽  
Gabriele Tonni ◽  
Silvia Asioli ◽  
Veronica Barbieri ◽  
...  
2018 ◽  
Vol 37 (5) ◽  
pp. 377-386 ◽  
Author(s):  
Moupali Ghosh ◽  
Nelofar Islam ◽  
Arindam Ghosh ◽  
Priyanka Maity Chaudhuri ◽  
Koushik Saha ◽  
...  

2009 ◽  
Vol 205 (7) ◽  
pp. 494-497 ◽  
Author(s):  
Yoo-Duk Choi ◽  
Sung-Sun Kim ◽  
Ji-Shin Lee ◽  
Jong-Hee Nam ◽  
Chan Choi ◽  
...  

2017 ◽  
Vol 8 (2) ◽  
pp. 89-92
Author(s):  
Rema Nambiar ◽  
Dinesh Nayak ◽  
Krupa H Shah ◽  
Shashikala K Bhat

ABSTRACT Congenital pulmonary airway malformation (CPAM) is a rare developmental lung abnormality. It is also referred as a congenital cystic adenomatoid malformation. The exact etiology is not known yet. The majority of cases are detected during targeted prenatal scan or within 2 years of the birth. Here, we report a case of CPAM type II diagnosed at 23 weeks of gestation, the key diagnostic features of which were mediastinal shift and lung lesion. The fetus had transient polyhydramnios and pericardial effusion. Glucocorticoids were administered for threatened preterm labor and CPAM. Healthy neonate was delivered at term without any immediate neonatal complications. How to cite this article Bhat SK, Nambiar R, Nayak D, Shah KH. Prenatal Diagnosis and Postnatal Management of Congenital Pulmonary Airway Malformation. Int J Infertil Fetal Med 2017;8(2):89-92.


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