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An Unusual Case of Giant Cell Tumor of First Metatarsal: A Rare Case Report and Review of Literature

机译:第一Meta骨巨细胞瘤的罕见病例:罕见病例报告并文献复习

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摘要

Introduction:Giant cell tumor (GCT) or osteoclastoma is an osteolytic, mostly benign but locally aggressive tumor occurring in young adults at the epiphysis. Area of predilection is mainly long bones (85-90%). 4% of GCT are also found in iliac bone, spine and only 2% in hand (of which GCT phalanges are more common than metacarpal). GCT of metatarsal is a very rare occurrence with very few cases being reported so far. We report a case of GCT 1st metatarsal in a 40-year-old male which is a very rare entity. We shall discuss the clinical features, pathological and radiological hallmarks, and the various treatment modalities of such lesion.
机译:简介:巨细胞瘤(GCT)或破骨细胞瘤是一种溶骨性肿瘤,多为良性但局部侵袭性肿瘤,发生在成年人的骨physi中。偏爱区域主要是长骨头(85-90%)。在CT骨,脊柱中也发现了4%的GCT,手部仅发现2%(其中GCT指骨比掌骨更常见)。 CT骨的GCT很少发生,迄今为止报道的病例很少。我们报告了一例GCT 1 st tar骨的病例,该病例在40岁的男性中非常罕见。我们将讨论这种病变的临床特征,病理和放射学特征以及各种治疗方式。

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