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首页> 外文期刊>International Journal of Surgical Research >Ameloblastic Fibrosarcoma of Mandible in a Paediatric Patient- A Rare Case Report
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Ameloblastic Fibrosarcoma of Mandible in a Paediatric Patient- A Rare Case Report

机译:儿科患者下颌骨的成纤维细胞肉瘤-罕见病例报告

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Background: Ameloblastic fibro sarcoma is a tumour of odontogenic origin. It is frequently seen in the 3~(rd) and 4~(th) decade of life. Case report: We report a case of 17 years old female who presented with left lower jaw swelling. CT scan revealed a large expansile osteolytic soft tissue mass in mandible. The patient underwent left extended hemimandibulectomy. Grossly the large mass measured 16x9x6.5cm, destructing the underlying mandible. Microscopic examination revealed a biphasic tumor composed of islands of benign odontogenic epithelium in abundant mesenchymal component, mild nuclear pleomorphism, and occasional mitosis. Hence the diagnosis of Ameloblastic Fibrosarcoma- Low grade was made. On radiological and clinical follow up patient is free of tumor till date. Conclusions: Ameloblastic fibrosarcoma is rare tumor of paediatric age. Surgical excision is a treatment of choice.
机译:背景:成纤维细胞肉瘤是牙源性起源的肿瘤。它经常出现在生命的第3个和第4个十年中。病例报告:我们报告一例17岁女性,左下颌肿胀。 CT扫描显示下颌骨有较大的扩张性溶骨性软组织肿块。该患者接受了左半下颌大手术。总的来说,大块的尺寸为16x9x6.5cm,破坏了下颌骨。显微镜检查显示为双相性肿瘤,由良性牙源性上皮小岛组成,具有丰富的间充质成分,轻度的核多态性和偶发的有丝分裂。因此,作出了诊断为非成纤维细胞纤维肉瘤的等级。在放射学和临床随访中,患者迄今为止没有肿瘤。结论:成纤维细胞肉瘤是小儿时期罕见的肿瘤。手术切除是一种治疗选择。

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