下颌骨原发性恶性纤维组织细胞瘤:罕见病例报告及免疫组织化学分析

Takaaki Kamatani , Akihisa Horie , Hiroaki Ishii , Hideo Kasahara , Yoshiki Hamada , Yoshio Aida , Satoru Shintani
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引用次数: 4

摘要

我们提出一个罕见的恶性纤维组织细胞瘤(MFH)出现在一个74岁的日本妇女下颌骨。口腔内检查显示右下颌牙槽嵴臼齿区有单一溃疡。全景x线片显示右侧磨牙区不透明、透光区。计算机断层扫描显示皮质骨破坏肿块。组织学检查显示大量成纤维细胞样纺锤状细胞呈束状排列,分散的多核和单核细胞,细胞核奇异。中度核多形性明显,有丝分裂细胞较少。免疫组化检测结果显示,所有肿瘤细胞的vimentin和Ki-67均呈阳性,而所有肿瘤细胞的c-kit、CD34、平滑肌肌动蛋白、CD68、S100蛋白和因子VIII均呈阴性。病变诊断为故事型-多形型MFH。手术切除病变和邻近组织后,患者被转介到放射治疗继续治疗,并在近一年后保持健康。
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Primary malignant fibrous histiocytoma of the mandible: Report of a rare case with an immunohistochemical analysis

We present a rare case of a malignant fibrous histiocytoma (MFH) arising in the mandible of a 74-year-old Japanese woman. Intraoral examination revealed a single ulcer in the right mandibular alveolar ridge at the molar region. Panoramic radiographs revealed ill-defined radiopaque, radiolucent area in the right molar region. Computed tomography demonstrated a mass with cortical bone destruction. The histological examination revealed numerous fibroblast-like spindle-shaped cells arranged in a fascicular pattern and scattered multinucleated and mononuclear cells with bizarre nuclei throughout the lesion. Moderate nuclear pleomorphism was evident with few mitotic cells. The immunohistochemical techniques proved positive for vimentin of all tumor cells and Ki-67 of about half of the tumor cells and negative for c-kit, CD34, smooth muscle actin, CD68, S100 protein, and Factor VIII of all tumor cells. The lesion was diagnosed as a MFH of storiform-pleomorphic type. After surgical removal of the lesion and the adjacent tissues, the patient was referred to a radiotherapist for continuation of treatment and remains well almost a year later.

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