| Literature DB >> 23328150 |
Sunila Jain1, Prem Chopra, Alok Agarwal, Shweta Gogia, Arup Basu.
Abstract
Inflammatory myofibroblastic tumor (IMT) is an uncommon entity usually encountered among children and involving the lungs. Involvement of trachea, however, is extremely rare with only a few published case reports. The condition may present with deceptive clinical features. We report a case of tracheal IMT in a 23-year-old female who presented with clinical symptoms mimicking asthma. On further evaluation, she was detected to have a tracheal mass that was diagnosed as IMT on histopathology and was successfully treated surgically. This case report highlights the rarity and diagnostic challenge associated with the condition.Entities:
Mesh:
Year: 2013 PMID: 23328150 DOI: 10.1097/LBR.0b013e31827cd58f
Source DB: PubMed Journal: J Bronchology Interv Pulmonol ISSN: 1948-8270