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头皮原发性骨外骨肉瘤在免疫抑制个体中的表现:病例报告及文献复习。

Primary cutaneous osteosarcoma of the scalp in an immunosuppressed individual: A case report and review of the literature.

机构信息

Department of Dermatology, Dudley Group of Hospitals NHS Trust, Birmingham, UK.

Department of Histopathology, Sandwell and West Birmingham Hospital NHS Trust, Birmingham, UK.

出版信息

J Cutan Pathol. 2020 Jul;47(7):628-632. doi: 10.1111/cup.13661. Epub 2020 Feb 13.

Abstract

We report a case of a 76-year-old man presenting with a 12-month history of a solitary lesion on his scalp. The histopathology was consistent with a grade 2/3 osteosarcoma extending to the subcutis. Full-body imaging excluded any involvement of the underlying bony tissue or solid organ malignancy, thus a diagnosis of primary cutaneous osteosarcoma (PCO) was made. Given the exceedingly rare nature of PCO, we discuss the clinico-pathological features of this case and those previously reported in the literature.

摘要

我们报告了一例 76 岁男性患者,其头皮上有一处孤立性病变,病史长达 12 个月。组织病理学检查符合 2/3 级骨肉瘤,延伸至皮下组织。全身成像排除了任何潜在骨组织或实体器官恶性肿瘤的累及,因此诊断为原发性皮肤骨肉瘤(PCO)。鉴于 PCO 的罕见性质,我们讨论了该病例的临床病理特征以及文献中以前报道的特征。

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