| Literature DB >> 27438081 |
Dayu Huang1, Qinyun Ma1, Shaohua Wang1, Qi Ouyang2, Xiaofeng Chen1.
Abstract
Tracheal diverticulum is a clinical entity rarely reported in the literature. It can be congenital or acquired in origin, and most cases are asymptomatic, usually being discovered incidentally at CT scan. Therefore, treatment has not been widely reported. We present the case of a 30-year-old man with a 6-month history of repeatedly coughing and tracheobronchitis. CT scanning revealed the lesion. The patient underwent surgical resection of the tracheal diverticulum via a transcervical approach. Symptoms resolved after surgical treatment. Reexamination of the neck, chest, trachea, and lungs of the patient was performed with CT scan postoperative.Entities:
Keywords: paratracheal air cyst; tracheal diverticulum
Mesh:
Year: 2016 PMID: 27438081 DOI: 10.1002/hed.24538
Source DB: PubMed Journal: Head Neck ISSN: 1043-3074 Impact factor: 3.147