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小腿前侧原发性骨外骨肉瘤:病例报告及文献复习。

Primary cutaneous extraskeletal osteosarcoma of the pretibial leg: A case report and summary of the literature.

机构信息

Department of Pathology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio, USA.

Department of Dermatology, Wayne State University School of Medicine, Detroit, Michigan, USA.

出版信息

J Cutan Pathol. 2022 Jun;49(6):549-556. doi: 10.1111/cup.14194. Epub 2022 Jan 12.

Abstract

Primary cutaneous extraskeletal osteosarcoma is a rare tumor, with fewer than 30 known cases worldwide. We report the case of a 60-year-old female who presented with a solitary right pretibial nodule of 3 mm. She had no known comorbidities, trauma to the area, or prior malignancy. The biopsy specimen showed abundant mineralized osteoid, in which pleomorphic and spindled cells with anaplastic features were embedded. The osteoid matrix in this case contained overtly malignant cells, with frequent mitotic figures, as well as multinucleated giant cells. Immunohistochemistry and imaging led to the conclusion that this nodule represented a primary cutaneous extraskeletal osteosarcoma. The previously reported cases are variable in location, size, gross appearance, and clinical course. The prognosis of osteosarcoma is typically poor, with aggressive behavior; this, however, may be less severe in these strictly cutaneous tumors, though additional follow-up would be beneficial to determine long-term outcomes for the known cases. Ultimately, despite the fact that this is an extremely rare entity, primary cutaneous extraskeletal osteosarcomas should be considered when relevant.

摘要

原发性皮肤外骨骼骨肉瘤是一种罕见的肿瘤,全世界已知病例少于 30 例。我们报告了一例 60 岁女性患者,其右侧胫骨前有一个孤立性结节,大小为 3mm。她没有已知的合并症、该区域的创伤史或先前的恶性肿瘤。活检标本显示丰富的矿化骨样组织,其中嵌入了异型和梭形细胞,具有间变特征。在这种情况下,骨样基质中含有明显的恶性细胞,有频繁的有丝分裂象,以及多核巨细胞。免疫组织化学和影像学检查的结论是,该结节代表原发性皮肤外骨骼骨肉瘤。以前报道的病例在位置、大小、大体外观和临床过程方面各不相同。骨肉瘤的预后通常较差,具有侵袭性;然而,在这些严格的皮肤肿瘤中,情况可能不那么严重,但需要进一步随访以确定已知病例的长期结果。最终,尽管这是一种极其罕见的实体肿瘤,但在相关情况下应考虑原发性皮肤外骨骼骨肉瘤。

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