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

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 reporte...

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Main Authors: Ozden Turan, I Murat Hirfanoğlu, Serdar Beken, Aydan Biri, Tünay Efetürk, Yildiz Atalay
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2011-06-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/1780
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author Ozden Turan
I Murat Hirfanoğlu
Serdar Beken
Aydan Biri
Tünay Efetürk
Yildiz Atalay
author_facet Ozden Turan
I Murat Hirfanoğlu
Serdar Beken
Aydan Biri
Tünay Efetürk
Yildiz Atalay
author_sort Ozden Turan
collection DOAJ
description 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.
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id doaj-art-c3c1e430d3a04f1aa4cfed57b86cd0de
institution DOAJ
issn 0041-4301
2791-6421
language English
publishDate 2011-06-01
publisher Hacettepe University Institute of Child Health
record_format Article
series The Turkish Journal of Pediatrics
spelling doaj-art-c3c1e430d3a04f1aa4cfed57b86cd0de2025-08-20T03:00:54ZengHacettepe University Institute of Child HealthThe Turkish Journal of Pediatrics0041-43012791-64212011-06-01533Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literatureOzden Turan0I Murat HirfanoğluSerdar BekenAydan BiriTünay EfetürkYildiz AtalayDivision of Neonatology, Department of Pediatrics, Gazi University, Faculty of Medicine, Ankara, Turkey. 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. https://turkjpediatr.org/article/view/1780
spellingShingle Ozden Turan
I Murat Hirfanoğlu
Serdar Beken
Aydan Biri
Tünay Efetürk
Yildiz Atalay
Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature
The Turkish Journal of Pediatrics
title Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature
title_full Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature
title_fullStr Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature
title_full_unstemmed Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature
title_short Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature
title_sort prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13 case report and review of the literature
url https://turkjpediatr.org/article/view/1780
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