Respiratory Medicine Case Reports (Jan 2014)

A rare tumor of trachea: Inflammatory myofibroblastic tumor diagnosis and endoscopic treatment

  • Mehmet Akif Özgül,
  • Ümran Toru,
  • Murat Acat,
  • Güler Özgül,
  • Erdoğan Çetinkaya,
  • H. Erhan Dinçer,
  • Derya Özden Omaygenç,
  • Halide Nur Ürer

DOI
https://doi.org/10.1016/j.rmcr.2014.10.001
Journal volume & issue
Vol. 13, no. C
pp. 57 – 60

Abstract

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Inflammatory myofibroblastic tumors (IMTs) are rare childhood neoplasms, with benign clinical course. Although etiology of IMTs are not clear, recent studies have reported that IMT is a true neoplasm rather than a reactive or inflammatory lesion. IMTs are rarely seen in adults and tracheal involvement is also rare both in adults and also in children. We describe a 16-year old female patient who was misdiagnosed and treated as asthma in another center for a few months and presented with acute respiratory distress due to upper airway obstruction. Computerized tomography (CT) of the chest and rigid bronchoscopy revealed a mass lesion that was nearly totally obliterating tracheal lumen. Bronchoscopic resection was performed under general anesthesia and the final pathological diagnosis was tracheal IMT.

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