[Inflammatory myofibroblastic tumor of the temporal bone with case report and literature review].

Yongqing Guo, Yongjun Hong, Yanfei Deng
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引用次数: 0

Abstract

Objective: To study the clinical presentation, imaging characteristics, intraoperative findings, and histopathologic features of inflammatory myofibroblastic tumor of the temporal bone.

Method: The clinical information of 1 case was reported and the literatures were also reviewed. The specimens were prepared for immunohistochemical staining and light microscopy.

Result: The lesions were locally aggressive with extensive bony erosion. Histologically, the tumor was composed of spindle cells and large number of chronic inflammatory cells. Immunohistochemical stains demonstrated Vimentin, SMA and CD68 were positive meanwhile S-100 and CK were negative.

Conclusion: Inflammatory myofibroblastic tumor of the temporal bone are rare lesions with a potential of local recurrence. Therapy should consists of surgical excision with steroids reserved for residual or intracranial disease or in patients in whom surgery is not an option.

[颞骨炎性肌成纤维细胞瘤附病例报告及文献复习]。
目的:探讨颞骨炎性肌成纤维细胞瘤的临床表现、影像学特点、术中表现及组织病理学特征。方法:报告1例患者的临床资料并复习文献。制备标本进行免疫组织化学染色和光镜检查。结果:病变具有局部侵袭性,伴有广泛的骨侵蚀。组织学上,肿瘤由梭形细胞和大量慢性炎症细胞组成。免疫组化染色显示Vimentin、SMA、CD68阳性,S-100、CK阴性。结论:颞骨炎性肌成纤维细胞瘤是一种罕见的病变,有局部复发的可能。治疗应包括手术切除和类固醇保留对残留或颅内疾病或患者的手术不是一个选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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