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Journal Information

Online ISSN
1305-3124

Established
1993

Editors-in-Chief
​Cihat Şen, ​Nicola Volpe

Editors
Daniel Rolnik, Mar Gil, Murat Yayla, Oluş Api

Statistics Editor
Resul Arısoy

Article info

Congenital cystic adenomatoid malformation: a case report. Perinatal Journal 2014;22(3):SE34 DOI: 10.2399/prn.14.S001084

Author(s) Information

Sevcan Arzu Arınkan,
Resul Arısoy,
Emre Erdoğdu,
Oya Demirci,
Oya Pekin,
Pınar Kumru,
Murat Muhçu

  1. S.B. Zeynep Kamil Kadın ve Çocuk Hastalıkları Eğitim ve Araştırma Hastanesi, Perinatoloji Kliniği- İstanbul TR
Correspondence

Murat Muhçu, S.B. Zeynep Kamil Kadın ve Çocuk Hastalıkları Eğitim ve Araştırma Hastanesi, Perinatoloji Kliniği- İstanbul TR,

Publication History
Conflicts of Interest

No conflicts declared.

Objective 
It is aimed to present a case of type 1 congenital cystic adenomatoid malformation which is prenatally diagnosed,and to discuss the management in these cases.
Case 
A 26-year-old gravida 1 patient was referred to our clinic at 20 weeks gestation. A detailed ultrasound scan was revealed that multiple anechoic cystic lesions at right lung. No additional anomaly was detected during the examinations of other systems.Type 1 congenital cystic adenomatoid malformation was diagnosed. Parents were informed about the fetal prognosis. Patient lost the follow-up and after two months, she applied to emergency with the complaint of pain. There was no fetal heart rate at the ultrasound examination and fetus was delivered vaginally.
Conclusion 
The differential diagnosis of type 1 congenital cystic adenomatoid malformation and the presence of concomitant anomalies are important for the management of these cases. The prognosis is good in cases with type 1 congenital cystic adenomatoid malformation without any other accompanying anomalies. Conservative management should be applied to these patients.
Keywords

Congenital cystic adenomatoid malformation, Prenatal diagnosis, Management

File/Dsecription
Figure 1
CCAM type 1
Figure 2
CCAM Type 1