SavedAdd your journal

Journals / İzmir Tepecik Eğitim Hastanesi Dergisi / 2014 / Cilt: 24 - Sayı: 1

Congenıtal cystıc adenomatoıd malformatıon of the lung: Prenatal and postnatal evaluation

Akciğerin konjenital kistik adenomatoid malformasyonu: Prenatal ve postnatal değerlendirme

Güray ÖNCEL
Dilek ÖNCEL
Erkan YILMAZ
Pages
63–67
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The patient was operated due to respiratory distress and the lesion was totally resected.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Congenital cystic adenomatoid malformation (CCAM) of lung is a rare congenital cystic lung lesion..
📊
Key Findings & Data:We report a case of CCAM (Stocker type 1) with a brief review of literature.
💡
Conclusion & Impact:The patient was operated due to respiratory distress and the lesion was totally resected.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Congenital cystic adenomatoid malformation (CCAM) of lung is a rare congenital cystic lung lesion.. We report a case of CCAM (Stocker type 1) with a brief review of literature. The patient was diagnosed antenatally with fetal MR. As no other associated anomalies or fetal hydrops were observed, no intrauterine intervention was planned. The baby was born at 36 weeks of gestation with an Apgar score of 8 and O 2 saturation was 92%. He had respiratory distress and tachypnea.The diagnosis was confirmed with CT examination. The patient was operated due to respiratory distress and the lesion was totally resected.

Özet

Akciğerin konjenital kistik adenomatoid malformasyonu (KKAM) ender görülen konjenital kistik bir akciğer lezyonudur. Bu yazıda bir KKAM (Stocker tip 1) olgusu literatür bilgileri eşliğinde sunulmaktadır. Olgu fetal MR ile antenatal tanı almış- tır ve ek konjenital anomali veya hidrops saptanmadığından intrauterin girişim yapılmamıştır. 36 gebelik haftasında doğan olgunun Apgar skoru 8 ve O2 satürasyonu %92 olarak izlenmiştir. Solunum sıkıntısı ve takipne bulguları olan olgunun tanı- sı BT ile doğrulanmıştır. Olgu solunum sıkıntısı nedeniyle opere edilmiş ve lezyon tümüyle rezeke edilmiştir.

🔖

Cite This Article

ÖNCEL, G., ÖNCEL, D., YILMAZ, E. (2014). Congenıtal cystıc adenomatoıd malformatıon of the lung: Prenatal and postnatal evaluation. İzmir Tepecik Eğitim Hastanesi Dergisi, Cilt: 24 - Sayı: 1, 63–67. https://ajindex.com/articles/216320

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (6)

  1. Chikkannaiah P, Kangle R, and Hawal M. Congenital cystic adenomatoid malformation of lung: Report of two cases with review of literature. Lung India. 2013; 30: 215-218.
  2. Jain A, Anand K, Singla S and Kumar A. Congenital Cystic Lung Diseases. J Clin Imaging Sci. 2013; 3: 5-11.
  3. Turhan NÖ, Simavlı S,Sarı U, Keskin EA,Gümüş İİ,Kamalak Z. Akciğerin kistik adenomatoid malformayonu; olgu sunumu ve literatür taraması.Yeni Tıp Dergisi 2010;27:184-6. Stocker JT. Congenital pulmonary airway malformation: A new name and an expanded classification of congenital cystic adenomatoid malformation of the lung. Histopathol. 2002;41:424-31.
  4. Kotecha S, Barbato A, Bush A, Claus F, Davenport M, Delacourt C,et al. Antenatal and postnatal management of congenital cystic adenomatoid malformation. Paediatr Respir Rev. 2012;13:162-70.
  5. Bozdağ Ş, Güven Ş, Ayanoğlu ÇY,Yavuz H, Ergüven M. Konjenital kistik adenomatoid malformasyon: bir vaka sunumu. Çocuk Dergisi 2012;12:193-7.
  6. Kozinszky Z, Keresztúri A, Pásztor N, Daru J, Sikovanyecz J, Kaiser L, et al. Magnetic resonance vs. sonographic imaging: diagnostics of a large congenital pulmonary airway malformation.Fetal Pediatr Pathol. 2013;31:55-9.