| Literature DB >> 25207108 |
Xinghua Tang1, Jian Zou1, Shixi Liu1.
Abstract
BACKGROUND: KARTAGENER SYNDROME (KS) IS A RARE CONGENITAL DISEASE CHARACTERISED BY A CLINICAL TRIAD OF SYMPTOMS: situs inversus, chronic rhinosinusitis, and bronchiectasis. Although congenital ciliary defect is recognised as the main cause of this syndrome, it remains difficult to treat the associated airway infection. CASE REPORT: A 17-year-old female patient presented with repeated refractory airway infection. She also had bronchiectasis and situs inversus. Electron microscopic evaluation of her nasal mucosa revealed ciliary defect and confirmed the diagnosis of KS. She underwent functional endoscopic sinus surgery (FESS) followed by long-term postoperative debridement of the sinonasal cavity. This treatment reduced chronic rhinosinusitis and protected against subsequent airway infection in a 7-year follow-up.Entities:
Keywords: Kartagener syndrome; endoscopy; primary ciliary dyskinesia; sinusitis; surgery
Year: 2013 PMID: 25207108 PMCID: PMC4115961 DOI: 10.5152/balkanmedj.2013.8152
Source DB: PubMed Journal: Balkan Med J ISSN: 2146-3123 Impact factor: 2.021