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Journals / İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi / 2012 / Cilt: 2 - Sayı: 3

An uncommon cause of respiratory distress in infancy: Right aortic arch anomaly

Sütçocukluğu döneminde solunum sıkıntısının ender bir nedeni: Sağ arkus aorta anomalisi

Mahmut DOĞRU
Tayfur GİNİŞ
İlknur BOSTANCI
Pages
191–193
DOI
—
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AI Summary & Key Takeaways

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

Anatomical abnormalities should be considered in cases with wheezing persisting since birth which does not respond to treatment with bronchodilators.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Right aortic arch anomaly is a rare vascular pathology.
📊
Key Findings & Data:It may cause respiratory and gastrointestinal tract symptoms by compressing adjacent structures.
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Conclusion & Impact:Anatomical abnormalities should be considered in cases with wheezing persisting since birth which does not respond to treatment with bronchodilators.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Right aortic arch anomaly is a rare vascular pathology. It may cause respiratory and gastrointestinal tract symptoms by compressing adjacent structures. Here, we presented a case who admitted with complaints of rapid breathing, cough and wheezing in our clinic who was diagnosed as right aortic arch anomaly. Anatomical abnormalities should be considered in cases with wheezing persisting since birth which does not respond to treatment with bronchodilators.

Özet

Sağ arkus aorta anomalisi ender görülen bir vasküler patolojidir. Anatomik olarak bası yaparak solunum ve gastrointestinal sistem semptomlarına yol açabilir. Burada hızlı nefes alıp verme, öksürük ve hışıltı yakınmalarıyla başvuran ve sağ arkus aorta anomalisi tanısı konulan olgu sunulmuştur. Yenidoğan döneminde başlayan ve bronkodilatatör tedaviye yanıtsız hışıltılı olgularda anatomik bozukluklar akla gelmelidir.

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Cite This Article

DOĞRU, M., GİNİŞ, T., BOSTANCI, İ. (2012). An uncommon cause of respiratory distress in infancy: Right aortic arch anomaly. İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, Cilt: 2 - Sayı: 3, 191–193. https://ajindex.com/articles/268711

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References (9)

  1. Kocis KC, Midgley FM, Ruckman RN. Aortic arch complex anomalies: 20-year experience with symptoms, diagnosis, associated cardiac defects, and surgical repair. Pediatr Cardiol 1997;18:127-132.
  2. Russell HM, Backer CL. Pediatric thoracic problems: patent ductus arteriosus, vascular rings, congenital tracheal stenosis, and pectus deformities. Surg Clin North Am 2010;90(5):1091-113.
  3. Backer CL, Mavroudis C. Congenital heart surgery nomenclature and database project: vascular rings, tracheal stenosis, pectus excavatum. Ann Thorac Surg 2000;69:308-318.
  4. VanDyke CW, White RD. Congenital abnormalities of the thoracic aorta presenting in the adult. J Thorac Imaging 1994;9:230-45.
  5. Kınoğlu B, Sarıoğlu T, Saltık L, Özkara A, Sarıoğlu A, Bilal MS ve ark. Vasküler Ring: Cerrahi Tedavi Ve Sonuçlar. Göğüs Kalp Damar Cerrrahisi Dergisi 1997;5:44-51
  6. Fındık S, Erkan L, Uzun O, Akan H, Atıcı AG, Bayrak M. Kliniğimizde sağ arkus aorta tanısı alan hastaların radyolojik ve klinik özellikleri. Toraks Dergisi 2005;6(1):13-18
  7. Pickhardt PJ, Siegel MJ, Gutierrez FR. Vascular rings in symptomatic children: Frequency of chest radiographic findings. Radiology 1997;203:423-426
  8. Humphrey C, Duncan K, Fletcher S. Decade of experience with vascular rings at a single institution. Pediatrics 2006;117(5):903-8.
  9. Okutan O, Kartaloğlu Z, Çalışkan T, Kunter E, Mutlu H, İlvan A. Sağ aortik ark anomalisi. Akciğer Arşivi 2005;6:120-122.