Cover image of the article: Mediastinal Tuberculous Lymphadenitis Presenting as a Mediastinal Mass with Dysphagia: A Case Report

Image Credit:I J Radiol

Mediastinal Tuberculous Lymphadenitis Presenting as a Mediastinal Mass with Dysphagia: A Case Report

Authors

Füsun Şahin1,*, A Yerlioğlu1, P Yıldız2
1Department of Chest Diseases, Yedikule Chest Diseases and Thoracic Surgery Research and Training Hospital, İstanbul, Turkey
2Associate Professor, Department of Chest Diseases, Yedikule Chest Diseases and Thoracic Surgery Research and Training Hospital, İstanbul, Turkey
*Corresponding Author: Department of Chest Diseases, Yedikule Chest Diseases and Thoracic Surgery Research and Training Hospital, İstanbul, Turkey. Tel: +902126641700, Fax: +902125472233, E-mail: fusunsahin19700@hotmail.com Email: fusunsahin19700@hotmail.com

Iranian Journal of Radiology:Vol. 8, issue 2; e93935
Published online:Jun 30, 2011
Article type:Case Report
Received:May 18, 2019
Accepted:Jun 30, 2011
How to Cite:Şahin F, Yerlioğlu A, Yıldız P. Mediastinal Tuberculous Lymphadenitis Presenting as a Mediastinal Mass with Dysphagia: A Case Report. I J Radiol. 2011;8(2):e93935. doi:

Abstract

Mediastinal tuberculous lymphadenitis is a rare disease in adults. Dysphagia as the accompanying symptom is even a rarer manifestation. Cases with esophageal symptoms may present as esophageal ulceration, mucosal or submucosal mass, fistula or sinus formation, extrinsic compression or displacement of the esophagus. Extrinsic compression may radiologically or endoscopically present as a submucosal tumor. Our case is a 30-year-old woman with dysphagia for a month. Extrinsic compression was seen endoscopically on the mid-esophagus. On thoracic CT and MRI images, a multiloculated cystic/necrotic mass  5.5×4.8×3.1 cm in size consisting of multiple septa was located subcarinally in the middle mediastinum. In Wang needle aspiration, a mucopurulaent liquid was aspirated from the subcarinal localization by bronchoscopy. Diagnostic thoracotomy was carried out because histological and bacteriological examinations were not diagnostic. It was reported as tuberculous lymphadenitis pathologically. The control thoracic CT performed after antituberculous treatment showed complete regression of the mass. We herein report a rare form of tuberculous lymphadenitis.

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Copyright

© 2011, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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