Maxilla tuberosity malignant fibrous histiocytoma with giant fibroblastic cells: Case report and review of literature

K.A. Al-Salihi , K.A. Al-Jashamy , S. Ab Rahman , A.R. Samsudin
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引用次数: 4

Abstract

Malignant fibrous histiocytoma (MFH) of the maxilla is a rare neoplasm. A round 61 cases reported in the international literature since 1974. We present a rare case of primary MFH of the maxilla in the unusual location of maxilla in a 64-year-old man. The tumor was located in the left tuberosity of maxilla extending from the junction between soft and hard palate towards premolar area of edentulous ridge, and measured 7 cm × 6 cm. Histologically, it consisted of spindle-shaped, pleomorphic malignant cells in a storiform pattern associated with histiocyte-like cells and giant cells. Mitotic figures were frequent Immunohistochemically, most of the tumor cells were strongly positive for vimentin, and negative with S-100 protein, cytokeratin, actin, desmin, HMB45 and epithelial membrane antigen. Ultra structurally, the tumor have clearly shown spindle shaped fibroblastic and giant cells with well-known pleomorphic multi-segmented nuclei, prominent branching and often dilated rough endoplasmic reticulum (RER). Histopathological and ultra structural findings are consistent with high-grade MFH of the storiform/pleomorphic subtype. Four months later the patient came with residual/recurrent tumor that was confirmed histopathologically. The literature is briefly reviewed.

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上颌结节性恶性纤维组织细胞瘤伴巨大成纤维细胞:病例报告及文献复习
上颌骨恶性纤维组织细胞瘤是一种罕见的肿瘤。自1974年以来,国际文献共报道了61例病例。我们报告了一例罕见的上颌骨原发性MFH病例,该病例发生在一名64岁的男性上颌骨的异常位置。肿瘤位于上颌骨的左侧结节,从软腭和硬腭的交界处向无齿嵴的前臼齿区域延伸,长7cm×6cm。组织学上,它由纺锤形、多形性恶性细胞组成,呈存储状,与组织细胞样细胞和巨细胞相关。免疫组化显示有丝分裂现象频繁,大多数肿瘤细胞波形蛋白强阳性,S-100蛋白、细胞角蛋白、肌动蛋白、结蛋白、HMB45和上皮膜抗原阴性。在超微结构上,肿瘤清楚地显示出梭形成纤维细胞和巨细胞,具有众所周知的多形性多节细胞核、突出的分支和经常扩张的粗糙内质网(RER)。组织病理学和超微结构检查结果与存储型/多形性亚型的高级别MFH一致。四个月后,患者出现残留/复发肿瘤,经组织病理学证实。对文献进行了简要回顾。
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