Abstract
Inflammatory myofibroblastic tumors IMTs are clinico-pathologically distinctive but biologically controversial entities; they rarely affect the head and neck region and usually follow a benign clinical course after radical excision. We reviewed the literatures of IMTs and present a rare case of IMT arising from the maxillary paranasal sinus of an 11-year-old girl. Moreover, we elaborate on the morpho-immunophenotypic characteristics of this lesion. Microscopic examination revealed a spindle cell proliferation set in a highly vascular stroma with numerous inflammatory cells. Tumor cells were immunoreactive for vimentin, and smooth muscle actin, negative for desmin, S-100, p53, Cyclin D1, and bcl-2. The potential neoplastic nature of this lesion was substantiated by the strong diffuse immuno-expression of ALK-1 protein, a marker that has been linked to neoplastic transformation. The lesion was excised completely by a CO2 LASER as a new treatment modality and the patient manifested no evidence of disease recurrence at 10-months recall.
Article Type
Case Report
First Page
623
Last Page
627
Recommended Citation
Al-Sindi, Khalid; Al-Shehabi, Mohamed H.; and Al-Khalifa, Salman A.
(2007)
"Inflammatory myofibroblastic tumor of paranasal sinuses,"
Saudi Medical Journal: Vol. 28:
Iss.
4, Article 25.
DOI: https://doi.org/10.15537/1658-3175.3870