Journals / Journal of Clinical and Analytical Medicine / 2014 / Cilt: 5 - Sayı: 6

Pektus Karinatus Deformitesinin Eşlik Ettiği Kartagener Sendromu

A Case of the Kartagener Syndrome Accompanied by Pectus Carinatus Deformity

Pages
519–520
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

In the literature it is mentioned that KS can be withrare togetherness but patient with thoracic deformities were not encountered.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A seven year old female patient diagnosed as a Kartagener Syndrom (KS) by thefindings of clinical and radiological, was brought to the hospital with the complaints such as expectoration sputum often, cough and fever.
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Key Findings & Data:Situs inversus totalis,pansinusitis, destroyed right lower lobe, bronchiectasis in the left middle lobe andpectus carinatus deformity were detected in the physical examination and radiological investigations of the patient.
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Conclusion & Impact:In the literature it is mentioned that KS can be withrare togetherness but patient with thoracic deformities were not encountered.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

A seven year old female patient diagnosed as a Kartagener Syndrom (KS) by thefindings of clinical and radiological, was brought to the hospital with the complaints such as expectoration sputum often, cough and fever. Situs inversus totalis,pansinusitis, destroyed right lower lobe, bronchiectasis in the left middle lobe andpectus carinatus deformity were detected in the physical examination and radiological investigations of the patient. Although long-term medical therapy pulmonary symptoms couldn t get under control. Because of this right lower lobectomywas performed to the patient. In the literature it is mentioned that KS can be withrare togetherness but patient with thoracic deformities were not encountered.

Özet

Klinik ve radyolojik olarak Kartagener Sendromu (KS) tanısı konulmuş olan yedi yaşındaki kız çocuk hasta; sık balgam çıkarma, öksürük, yüksek ateş şikayeti ile getirildi. Hastanın fizik muayene ve radyolojik incelemelerinde; situs inversus totalis, yaygın sinüzit, harab olmuş sağ alt lob, sol orta lobda bronşektazi, pektus karinatus deformitesi saptandı. Uzun süreli medikal tedaviye rağmen pulmoner semptomlar kontrol altına alınamadığı için hastaya sağ alt lobektomi yapıldı. Literatürde KS ile nadir birlikteliklerden bahsedilmiş ancak toraks deformiteli olguyarastlanmamıştır.

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Cite This Article

KORKMAZ, C., TOKUR, M., TOKUR, N., YENİBERTİZ, D. (2022). Pektus Karinatus Deformitesinin Eşlik Ettiği Kartagener Sendromu. Journal of Clinical and Analytical Medicine, Cilt: 5 - Sayı: 6, 519–520. https://ajindex.com/articles/561166

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References (7)

  1. Afzelius BA. Immotile cilia syndrome: past, present and prospects for the future. Thorax 1998;53(10):894-7
  2. Behrman RE, editor. Nelson Texbook of Pediatrics. 17th ed. Philadelphia: wb Saunders; 2000. p.1391
  3. De Iongh RU, Rutland J: Ciliary defects in healthy subjects, bronchiectasis, and primary ciliary dyskinesia. Am J Respir Crit Care Med 1995;151(5):1559-67
  4. Webber BA, Pryor JA, editors. Bronchiectasis, primary ciliary dyskinesia and cystic fibrosis, Physiotherapy for Respiratory and Cardiac Problems. Tokyo: Churchill Livingstone; 1993.p.402-4
  5. Agasthian T, Deschamps C, Trastek VF, Allen MS, Pairolero PC. Surgical management of bronchiectasis. Ann Thorac Surg 1996;62(4):976-8
  6. Yakan B, Mirici A, Görgüner M, Girgiç M, Mısırlıoğlu F. Kifoskolyoz ve Kongenital Kardiak Anomaliler ile Birlikte Seyreden Kartagener Sendromlu Bir Hastanın Silya Ultrastrüktürü. Türkiye Klinikleri Tıp Dergisi 1996;16(6):458-60
  7. Shamberger RC. Chest wall deformities. In: Shields TW,LoCicero III J, Ponn RB, editors. General Thoracic Surgery. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2000.p.535-61.