[Tracheocele: a rare cause of pharyngeal disorders].

Ann Otolaryngol Chir Cervicofac

Service d'ORL et de chirurgie cervico-faciale, Hôpital Bretonneau, CHU de Tours, France.

Published: October 2002

A 40-year-old woman with an uneventful history consulted for an episode of cervical swelling and pharyngeal disorders with sensation of a foreign body. Cervical and ENT examination was normal. The barium swallow showed a normal esophagus and the CT scan showed an air image in the right side of the trachea. The diagnosis of tracheocele was made at surgery and was confirmed by histology. Clinical, endoscopic, and radiologic outcome was favorable three months after surgical resection of the diverticulum. Tracheocele is rarely reported in the literature. It results from a congenital or acquired weakness of the tracheal wall. The right side is involved more frequently. No specific signs or symptoms have been identified. Diagnosis is often based on CT findings. Surgery confirms the diagnosis and allows resection.

Download full-text PDF

Source

Publication Analysis

Top Keywords

[tracheocele rare
4
rare pharyngeal
4
pharyngeal disorders]
4
disorders] 40-year-old
4
40-year-old woman
4
woman uneventful
4
uneventful history
4
history consulted
4
consulted episode
4
episode cervical
4

Similar Publications

BACKGROUND Tracheocele are rarely encountered air cysts formed due to tracheal wall outpouching through a weak vantage point. The majority are acquired in the adult population and are associated with conditions that weaken the tracheal wall. Most tracheoceles are diagnosed incidentally since many are asymptomatic or present with nonspecific symptoms.

View Article and Find Full Text PDF

Tracheocele: A Rare Entity.

Iran J Otorhinolaryngol

July 2022

Department of ENT and Cervicofacial Surgery. Habib Bourguiba's Teaching Hospital, El Ferdaous Avenue, 3029 Sfax, Tunisia. University of Sfax.

Introduction: Tracheocele or tracheal diverticulum is an uncommon benign entity that can be congenital or acquired. It is usually diagnosed incidentally on cervicothoracic imaging. Our aim is to describe the etiopathogenic, clinical and paraclinical features of the tracheocele as well as its therapeutic modalities.

View Article and Find Full Text PDF

Huge Tracheal Diverticulum in a Patient with Mounier-Kuhn Syndrome.

Eur J Case Rep Intern Med

June 2016

Respiratory Unit, San Paolo Hospital, Dept. of Scienze della Salute, Università degli Studi di Milano, Milan, Italy.

Article Synopsis
  • - Tracheal diverticulum is a rare, benign condition often associated with tracheobronchomegaly (TBM), a disorder known for the dilation of the trachea and bronchi, which can weaken the trachea and lead to complications like mucosal herniation.
  • - A reported case involved a patient with TBM who had the largest recorded tracheal diameter for this syndrome, diagnosed using bronchoscopy and 3D CT reconstruction.
  • - Diagnosing tracheal diverticulum is important in patients with chronic cough and bronchial infections, and it must be differentiated from other conditions like laryngocele and Zenker's diverticulum, with bronchoscopy and CT being effective diagnostic
View Article and Find Full Text PDF

Tracheocele presenting with intermittent dysphonia: a case report.

Indian J Otolaryngol Head Neck Surg

March 2015

Department of Otolaryngology and Head and Neck Surgery, Apollo Hospitals, 21, Greams Lane, Off., Greams Road, Chennai, 600 006 Tamilnadu India.

We report a rare case of tracheocele presenting in an ENT setting. The referral was made on the basis of intermittent dysphonia. The aim of this report is to document the rare condition of tracheocele on the right side and to help raise the level of its awareness among the otolaryngologists.

View Article and Find Full Text PDF

Giant tracheocele with multiple congenital anomalies.

Ear Nose Throat J

May 2012

Department of Otorhinolaryngology-Head and Neck Surgery, National University Health System, Republic of Singapore.

Tracheocele--an outpouching of tracheal mucous membrane--is an uncommon entity. It can occur as a congenital or acquired form. The congenital entity remains mostly dormant until adulthood, and then it typically presents as a herniation with multiple air-filled sacs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!