Giant cell variant of extraskeletal osteosarcoma

Sufian Zaheer, Durre Aden, Sunil Ranga
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引用次数: 0

Abstract

The giant cell-rich (GCR) variant of extraskeletal osteosarcoma (ESOS) is a malignant soft-tissue lesion without primary bony involvement. The tumor cells are highly pleomorphic and produce an osteoid matrix, whereas numerous giant cells are present throughout the mass. We describe an unusual case of a 38-year-old female patient who presented with a recurrent gluteal mass. With the help of histomorphological findings and immunohistochemistry (IHC), a final diagnosis of a GCR variant of ESOS arises from the gluteal soft tissue with bony involvement. These malignancies are extremely aggressive and have a high likelihood of recurrence and metastasis; therefore, early detection is crucial for successful management. Standard treatment options include surgery and chemotherapy, and patients should be closely monitored following treatment. With the help of histomorphological findings and IHC, a final diagnosis of a GCR variant of ESOS arises from the gluteal soft tissue with bony involvement. This case is reported to highlight the fact that similar morphology of giant cell osteosarcoma can rarely be seen in soft tissue, and this entity should be kept in mind by the reporting pathologist.
骨外骨肉瘤的巨细胞变异
富巨细胞(GCR)变异的骨外骨肉瘤(ESOS)是一种没有原发性骨受累的恶性软组织病变。肿瘤细胞高度多形性,产生类骨基质,而大量巨细胞遍布肿块。我们描述了一个不寻常的情况下,一个38岁的女性患者谁提出了一个复发的臀部肿块。在组织形态学检查和免疫组化(IHC)的帮助下,最终诊断为GCR变异的ESOS来自臀部软组织并伴有骨受累。这些恶性肿瘤极具侵袭性,有很高的复发和转移的可能性;因此,早期发现对成功治疗至关重要。标准治疗方案包括手术和化疗,治疗后应密切监测患者。在组织形态学检查和免疫组化检查的帮助下,最终诊断为GCR变异的ESOS起源于臀部软组织并伴有骨受累。本病例的报道强调了一个事实,即在软组织中很少看到类似的巨细胞骨肉瘤形态,报告的病理学家应牢记这一实体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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