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首页> 外文期刊>Diagnostic pathology >Malignant perivascular epithelioid cell tumor (PEComa) of the femur: a case report and literature review
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Malignant perivascular epithelioid cell tumor (PEComa) of the femur: a case report and literature review

机译:股骨恶性血管周围上皮样细胞瘤(PEComa):一例报告并文献复习

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摘要

Background We describe a case of malignant perivascular epithelial cell tumor (PEComa) arising primarily in the distal left femur of a 47-year-old male. Case presentation The patient presented with pain accompanied by progressive swelling of his left thigh. Computed tomography (CT) scan and magnetic resonance imaging (MRI) revealed an osteolytic lesion. Curettage of the lesion was reported as a clear cell tumor with recommendation for exclusion of a metastatic clear cell carcinoma. However, thorough examinations did not find any primary site elsewhere, apart from the presence of bilateral pulmonary metastases. Evaluation of the submitted H & E slides identified a malignant PEComa which was further confirmed by subsequent immunohistochemical study. Conclusions The occurrence of PEComa as a primary bone lesion is extremely rare. We present here a malignant PEComa of the distal left femur, and summarize the clinicopathological characteristics of this rare entity with literature review. Virtual slides The virtual slide (s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5729035221600545 webcite.
机译:背景我们描述了一例恶性血管周围上皮细胞瘤(PEComa)的病例,主要发生在47岁男性的左股骨远端。病例介绍患者出现疼痛并伴有左大腿进行性肿胀。计算机断层扫描(CT)扫描和磁共振成像(MRI)显示溶骨性病变。据报道,该病的刮除是透明细胞肿瘤,建议排除转移性透明细胞癌。但是,除了双侧肺转移灶外,彻底检查未发现其他任何主要部位。对提交的H&E载玻片进行评估后,发现恶性PEComa,随后的免疫组织化学研究进一步证实了该恶性。结论PEComa作为原发性骨病变的发生极为罕见。我们在这里介绍了左股骨远端的恶性PEComa,并通过文献综述总结了这种罕见实体的临床病理特征。虚拟幻灯片可以在此处找到本文的虚拟幻灯片:http://www.diagnosticpathology.diagnomx.eu/vs/5729035221600545网站。

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