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Journals / Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi / 2013 / Cilt: 10 - Sayı: 38

Congenital Cystic Adenomatoid Malformation As A Rare Cause Of Respiratory Distress In Newborn

Yenidoğanda Nadir Bir Solunum Sıkıntısı Nedeni: Konjenital Kistik Adenoid Malformasyon

Nurdan FETTAH
Dilek DİLLİ
Nuran UZUNALIÇ
Ayşegül ZENCİROĞLU
Nurullah OKUMUŞ
İbrahim KARAMAN
Pages
1602–1603
Publication Date
2013-04-01
DOI
—
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AI Summary & Key Takeaways

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

Lobectomy has been recommended in symptomatic. patients; whereas surgical intervention may be delayed in asymptomatic patients for 6-12 months.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Congenital cystic adenomatoid malformation CCAM is a rare lung disorder developed as a result of the improper fusion of the bronchial buds with the alveolar mesenchyme during embryological development.
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Key Findings & Data:Depending on the type of lesion, CCAM tissue pressure in newborns may cause respiratory distress and may later manifest itself as recurrent pulmonary infections in young adults.
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Conclusion & Impact:Lobectomy has been recommended in symptomatic. patients; whereas surgical intervention may be delayed in asymptomatic patients for 6-12 months.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Konjenital Kistik Adenomatoid Malformasyon · Yenidoğan · Akciğer

Abstract

Congenital cystic adenomatoid malformation CCAM is a rare lung disorder developed as a result of the improper fusion of the bronchial buds with the alveolar mesenchyme during embryological development. Depending on the type of lesion, CCAM tissue pressure in newborns may cause respiratory distress and may later manifest itself as recurrent pulmonary infections in young adults. Lobectomy has been recommended in symptomatic. patients; whereas surgical intervention may be delayed in asymptomatic patients for 6-12 months.

Özet

Konjenital kistik adenoid malformasyon KKAM bronşiyal tomurcukların alveolar mezenşimle uygun şekilde birleşememesi sonucu ortaya çıkan akciğerin nadir görülen embryolojik gelişim bozukluğudur. Lezyonun tipine göre, KKAM fonksiyon gören pulmoner dokuya bası ile yenidoğanlarda solunum güçlüğüne yol açabilir veya genç erişkinde rekürren akciğer enfeksiyonu ile kendini gösterebilir. Semptomatik olgularda lobektemi önerilmekte, asemptomatik olgularda ise 6-12 aya kadar girişimin geciktirilebileceği bildirilmektedir.

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Cite This Article

FETTAH, N., DİLLİ, D., UZUNALIÇ, N., ZENCİROĞLU, A., OKUMUŞ, N., KARAMAN, İ. (2013). Congenital Cystic Adenomatoid Malformation As A Rare Cause Of Respiratory Distress In Newborn. Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, Cilt: 10 - Sayı: 38, 1602–1603. https://ajindex.com/articles/676715

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References (5)

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