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Mesenchymal chondrosarcoma of the orbit: A case report with 5?years of follow-up

机译:轨道的间充质软骨肉瘤:案例报告5?多年随访

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Mesenchymal chondrosarcoma is a rare orbital tumor. Several case reports of this rare tumor have been published in the literature but only 6 cases have documented a follow up of 5?years or more. We report a case of 28?year-old female who presented with left orbital mass. Computed Tomography (CT) revealed a lobulated mass in the superior extraconal space with dense intralesional calcification. Patient underwent complete resection of the mass and histopathology was suggestive of mesenchymal chondrosarcoma. He was given adjuvant radiotherapy and there was no recurrence or metastasis at 5?years of follow-up. The case highlights that a complete resection with adjuvant radiotherapy in cases of orbital mesenchymal chondrosarcoma offers excellent prognosis.
机译:间充质骨髓瘤是一种罕见的眶肿瘤。 有几个案例报告在文献中发表了这种罕见的肿瘤,但只有6个案件记录了5岁以下的时间或更长时间。 我们举报了28岁的案例?岁月的女性呈现出左侧轨道物质。 计算机断层扫描(CT)揭示了具有致密的腔内钙化的高级外部空间中的裂肿块。 患者接受了群众和组织病理学的完全切除,旨在是间充质软骨菌瘤的暗示。 他给予佐剂放射治疗,并且在5年后没有复发或转移。 这种情况强调,在轨道间充质软骨菌菌病例中具有佐剂放射治疗的完全切除,具有优异的预后。

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