z-logo
Premium
Inflammatory myofibroblastic tumor of the larynx
Author(s) -
Suh Sangil,
Seol Hae Young,
Lee Jean Hwa,
Lee Young Hen,
Kim TaikKun,
Lee Nam Joon,
Woo JeongSoo,
Kim In Sun
Publication year - 2006
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/hed.20413
Subject(s) - medicine , larynx , laryngoscopy , biopsy , lesion , head and neck , benign tumor , radiology , pathology , surgery , intubation
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. © 2006 Wiley Periodicals, Inc. Head Neck 28: 369–372, 2006

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom