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

被引:8
作者
Ozgul, Mehmet Akif [1 ]
Toru, Umran [2 ]
Acat, Murat [3 ]
Ozgul, Guler [4 ]
Cetinkaya, Erdogan [1 ]
Dincer, H. Erhan [5 ]
Omaygenc, Derya Ozden [6 ]
Urer, Halide Nur [7 ]
机构
[1] Yedikule Chest Dis & Thorac Surg Training & Res H, Dept Chest Dis, TR-34020 Istanbul, Turkey
[2] Dumlupinar Univ, Dept Chest Dis, Fac Med, Tavsanli Yolu 10 Km, TR-43100 Kutahya, Turkey
[3] Karabuk Univ, Dept Chest Dis, Fac Med, TR-78050 Karabuk, Turkey
[4] Bagcilar Educ & Res Hosp, Dept Chest Dis, TR-34200 Istanbul, Turkey
[5] Univ Minnesota, Div Pulm Allergy Sleep & Crit Care, Columbus, OH 43210 USA
[6] Yedikule Chest Dis & Thorac Surg Training & Res H, Dept Anesthesiol & Reanimat, TR-34020 Istanbul, Turkey
[7] Yedikule Chest Dis & Thorac Surg Training & Res H, Dept Pathol, TR-34020 Istanbul, Turkey
关键词
Inflammatory myofibroblastic tumor; Trachea; Bronchoscopy;
D O I
10.1016/j.rmcr.2014.10.001
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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. (C) 2014 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:57 / 60
页数:4
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