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Journals / Çocuk Dergisi / 2008 / Cilt: 8 - Sayı: 2

A rare cause of dyspnea in a newborn: Congenital lobar emphysema accompanying pulmonary interstitial emphysema

Yenidoğanda ender bir solunum sıkıntısı nedeni: Konjenital lober amfizem ve pulmoner interstisyel amfizem birlikteliği

Levent ELEMEN
Günbey Gökçe BASLO
Kıray Evrim BAŞ
Feriha ÖZ
Ergun ERDOĞAN
Pages
120–123
DOI
—
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AI Summary & Key Takeaways

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

Here we present a premature newborn, who had CLE and PIE together, and treated successfully with right upper lobectomy.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Congenital lobar emphysema (CLE) is the overinflation of one or more pulmonary lobes.
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Key Findings & Data:Diagnosis of CLE may be delayed in mild disease due to lack of life-threatening symptoms.
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Conclusion & Impact:Here we present a premature newborn, who had CLE and PIE together, and treated successfully with right upper lobectomy.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Ampiyem · Süt çocuğu · prematür

Abstract

Congenital lobar emphysema (CLE) is the overinflation of one or more pulmonary lobes. Diagnosis of CLE may be delayed in mild disease due to lack of life-threatening symptoms. Pulmonary interstitial emphysema (PIE), which is a collection of gases outside of the normal air passages is more frequent in premature infants who require mechanical ventilation. CLE or PIE may be the cause of permanent and severe dyspnea in newborn period. Surgical resection of the effected lobes is indicated in both unless symptoms resolve with conservative therapy. Here we present a premature newborn, who had CLE and PIE together, and treated successfully with right upper lobectomy.

Özet

Konjenital lober amfizem (KLA), bir akciğer lobunun olması gerekenden daha fazla havalanmasıyla karakterize doğumsal bir hastalıktır. Ender olarak birden fazla akciğer lobu etkilenebilir. Pulmoner interstisyel amfizem (PİA), genellikle pozitif basınçlı ventilasyon uygulanan prematüre bebeklerde havanın normal hava yollarının dışında birikmesi durumudur. KLA ve PİA yenidoğan döneminde solunum sıkıntısına yol açmaktadır. KLA’da ender olarak semptomların ortaya çıkışı altı aya kadar gecikebilir. Hafif vakalarda konservatif tedavi tercih edilirken, solunum sıkıntısının düzelmediği vakalarda cerrahi girişim gerekmektedir. Bu makalede yenidoğan döneminde tanısı konularak lobektomi uygulanmış bir KLA-PİA birlikteliği vakası tartışılmıştır.

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Cite This Article

ELEMEN, L., BASLO, G. G., BAŞ, K. E., ÖZ, F., ERDOĞAN, E. (2008). A rare cause of dyspnea in a newborn: Congenital lobar emphysema accompanying pulmonary interstitial emphysema. Çocuk Dergisi, Cilt: 8 - Sayı: 2, 120–123. https://ajindex.com/articles/151073

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