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Primary Sclerosing Epithelioid Fibrosarcoma of the Lung in a Patient with Lynch Syndrome

机译:林奇综合征患者的肺原发性硬化上皮样纤维肉瘤。

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摘要

Sclerosing epithelioid fibrosarcoma (SEF) is a rare neoplasm arising mostly in limbs and limb girdles, with a high rate of recurrence and a strong tendency to metastasize. This case study is of a 54-year-old woman with an asymptomatic mass in the upper lobe of the left lung detected by PET-CT when staging for Lynch syndrome-associated colon carcinoma. Histology of the resected tumor showed epithelioid cells arranged in nests, partly restiform within a zone of sclerosing fibrosis. Immunohistochemistry was positive for vimentin, epithelial membrane antigen, and S100-protein. Eight months after lung resection, the patient was diagnosed for basal cell carcinoma on her back. At the end of a two year follow-up period, she developed metastases to the mediastinum, vertebrae, ribs, femurs, pelvic bones, kidneys, and one lung, histologically all related to SEF. Here we report the first case of a SEF primarily arising from the lung and discuss it in the context of the current literature.
机译:硬化性上皮样纤维肉瘤(SEF)是一种罕见的肿瘤,多发于四肢和四肢带,复发率高,有很强的转移倾向。该病例研究是一名54岁的女性,在进行Lynch综合征相关的结肠癌分期时,PET-CT检测到左肺上叶无症状肿块。切除的肿瘤的组织学表现为上皮样细胞排列在巢中,在硬化性纤维化区域内部分呈网状。波形蛋白,上皮膜抗原和S100蛋白的免疫组织化学呈阳性。肺切除术后八个月,该患者被诊断为背部基底细胞癌。在两年的随访期末,她在组织学上发展为纵隔,椎骨,肋骨,股骨,骨盆骨,肾脏和一个肺的转移,从组织学上讲都与SEF有关。在这里,我们报告主要来自肺部的SEF的第一例,并在当前文献的背景下进行讨论。

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