Kartagener's syndrome: A rare condition diagnosed in a young male patient

Radiol Case Rep. 2024 Apr 19;19(7):2741-2744. doi: 10.1016/j.radcr.2024.03.067. eCollection 2024 Jul.

Abstract

Kartagener's Syndrome is a rare autosomal recessive genetic condition, that affects the structure and function of cilia and includes a condition of situs inversus, chronic sinusitis, and bronchiectasis associated sometimes with infertility. A young patient who had a long-time fever, cough, and infertility after a clinical evaluation performed a chest X-ray and a CT scan that revealed the unexpected condition of Situs Inversus Totalis (SIT). Imaging also showed bronchiectasis and sinusitis: all findings consistent with Kartagener's syndrome, confirmed a second time by the genetic test. This case highlights the importance of knowing and considering situs inversus in clinical practice, particularly when interpreting imaging studies and planning medical interventions. Furthermore, as situs inversus may be associated with cardiovascular and pulmonary pathologies in several syndromic conditions, such as Kartagener's syndrome in this case, these conditions should always be carefully examined.

Keywords: Case report; Diagnostic imaging; Kartagener's syndrome; Primary ciliary dyskinesia; Situs inversus totalis.

Publication types

  • Case Reports