Inflammatory myofibroblastic tumor of the larynx

被引:21
作者
Suh, SI
Seol, HY
Lee, JH
Lee, YH
Kim, TK
Lee, NJ
Woo, JS
Kim, IS
机构
[1] Korea Univ, Sch Med, Dept Diagnost Radiol, Guro Hosp, Seoul 152703, South Korea
[2] Korea Univ, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Seoul 152703, South Korea
[3] Korea Univ, Sch Med, Dept Pathol, Seoul 152703, South Korea
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2006年 / 28卷 / 04期
关键词
larynx; inflammatory myofibroblastic tumor; CT imaging; MR imaging; steroid therapy;
D O I
10.1002/hed.20413
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. Inflammatory myofibroblastic tumor, composed of myofibroblastic spindle cells with acute and chronic inflammatory cells, is an unusual, benign solid mass that mimics a neoplastic process. Methods. We report a rare case of a patient with a laryngeal inflammatory myofibroblastic tumor. Laryngoscopy demonstrated a submucosal mass involving the right false cord. The mass was a well-enhanced supraglottic lesion on CT scan. It showed medially high signal intensity and peripherally low signal intensity on T2-weighted MR images, and it displayed a high magnetization transfer ratio; before surgery, it was believed to be a malignant tumor. Laryngoscopic biopsy was performed. Pathologic features of the specimen were diagnostic for inflammatory myofibroblastic tumor. Results. Steroid therapy was chosen for further treatment. No recurrence was observed for 4 years. Conclusion. In patients with chronic hoarseness who have a malignant-looking submucosal laryngeal mass, inflammatory myofibroblastic tumor should be considered. Conservative surgery and steroid treatment are advocated because of laryngeal preservation. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:369 / 372
页数:4
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