Gasparotti Roberto, Zanetti Diego, Bolzoni Andrea, Gamba Paola, Morassi Maria L, Ungari Marco
Department of Radiology, University of Brescia, Brescia, Italy.
AJNR Am J Neuroradiol. 2003 Nov-Dec;24(10):2092-6.
Inflammatory myofibroblastic tumors include a diverse group of lesions characterized by inflammatory cell infiltration and variable fibrotic responses. Occurrence in the temporal bone is unusual. We present CT and MR imaging findings of an inflammatory myofibroblastic tumor of the temporal bone in a 26-year-old patient with repeated paroxystic episodes of rotatory vertigo that occurred over a few days. CT and MR imaging revealed a homogeneously enhancing soft-tissue mass of the right mastoid with bone erosion of the tegmen and extensive dural thickening. The mass resembled a malignant tumor, and the patient underwent an extended mastoidectomy through a retroauricular approach. Microscopic examination showed myofibroblastic spindle cells with mixed inflammatory infiltrate, and the pathologic diagnosis was inflammatory myofibroblastic tumor.
炎性肌纤维母细胞瘤包括一组多样的病变,其特征为炎性细胞浸润和不同程度的纤维化反应。发生于颞骨者较为罕见。我们报告了一名26岁患者的颞骨炎性肌纤维母细胞瘤的CT和MR成像表现,该患者在数天内反复出现发作性旋转性眩晕。CT和MR成像显示右侧乳突有均匀强化的软组织肿块,伴有 tegmen骨侵蚀和广泛的硬脑膜增厚。该肿块类似恶性肿瘤,患者通过耳后入路接受了扩大乳突切除术。显微镜检查显示肌纤维母细胞梭形细胞伴有混合性炎性浸润,病理诊断为炎性肌纤维母细胞瘤。