A Case Report: Seven-Year Follow-Up of a Patient With Kartagener Syndrome Undergoing Bilateral Lung Transplantation


Yilmaz E., Basaran F. C., Bindal M., TÜRKKAN S., Sahin M. F., Direk T., ...Daha Fazla

Transplantation Proceedings, cilt.58, sa.5, ss.934-938, 2026 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 58 Sayı: 5
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1016/j.transproceed.2026.04.026
  • Dergi Adı: Transplantation Proceedings
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, EMBASE, MEDLINE, Academic Search Ultimate (EBSCO)
  • Sayfa Sayıları: ss.934-938
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Kartagener syndrome (KS) is a rare genetic disorder inherited in an autosomal recessive manner. Bronchiectasis is a major contributor to the morbidity associated with this syndrome. In end-stage cases of KS, bilateral lung transplantation (DLuTx) is considered a viable treatment option. This case report presents a 7-year follow-up of a KS patient who developed end-stage respiratory failure and subsequently underwent DLuTx. The case includes both surgical and postoperative challenges, ultimately resulting in a significant improvement in the patient's quality of life.