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Low Grade Central Osteosarcoma-A Diagnostic Challenge

机译:低度中枢骨肉瘤-A诊断挑战

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Low Grade Central Osteosarcoma (LGCO) is a rare intramedullary and well differentiated variant of osteosarcoma with a betterprognosis than the more common conventional variant. It was frst described by Unni et al., in 1977. Due to its subtle histologicalfeatures of malignancy, it is diffcult to diagnose on biopsy. Even in the resection specimen it can be mistaken for lesions likefbrous dysplasia, desmoplastic fbroma, parosteal osteosarcoma and fbrosarcoma. Adequate sampling of the tumour is essentialto arrive at a correct diagnosis. Histological features such as cytological atypia, mitotic activity, permeation into the bone marrow,entrapment of the native bone, cortical disruption and soft tissue extension will help in the diagnosis of this tumour. We report acase of a 30-year-old man who presented with pain in the right hip of three months duration. On radiological evaluation, a lyticlesion was noted in the upper part of right femur and a possible diagnosis of locally aggressive giant cell tumour of bone wasproposed. On histopathological study of the resected upper part of the right femur, a diagnosis of LGCO was rendered.
机译:低度中央骨肉瘤(LGCO)是一种罕见的髓内且分化良好的骨肉瘤变体,其预后要比更常见的常规变体好。最早在1977年由Unni等人描述。由于其微妙的恶性组织学特征,很难通过活检进行诊断。即使在切除标本中,也可能将其误认为是纤维增生,增生性纤维瘤,骨旁骨肉瘤和纤维肉瘤。足够的肿瘤样本对于正确诊断至关重要。组织学特征,如细胞学上的异型性,有丝分裂活性,渗透到骨髓,天然骨的包埋,皮质破坏和软组织延伸,将有助于诊断该肿瘤。我们报告了一例30岁男子,他的右髋关节疼痛持续了三个月。经放射学评估,在右股骨的上部发现了溶胞病,并提出了可能诊断为局部侵袭性骨巨细胞瘤的建议。在对右股骨切除的上部进行组织病理学研究后,诊断为LGCO。

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