Sclerosing epithelioid fibrosarcoma of the chest wall

Sunhee Chang, Mee Joo, Kim Hanseong, Ji Yun Ryoo, Yeon Soo Kim, Sung-Soon Lee, Jae Yun Ro
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Abstract

Sclerosing epithelioid fibrosarcoma is an unusual variant of fibrosarcoma composed of epithelioid cells arranged in strands and nests in the background of a highly sclerotic collagenous stroma. Despite the relatively bland appearance and low mitotic activity, the tumor is capable of local recurrence and distant metastasis. We report a case of sclerosing epithelioid fibrosarcoma arising from the chest wall in a 26-year-old man. Microscopically, the tumor showed proliferation of round, oval, or angulated tumor cells in the sclerotic collagenous stroma. The tumor cells were small to medium in size, had pale eosinophilic cytoplasm and were arranged in cords, strands, and clusters. Immunohistochemically, the tumor cells were diffusely positive for vimentin, but negative for pan-cytokeratin, S100 protein, human melanoma black 45, CD34, smooth muscle actin, and desmin. The tumor cells showed paranuclear dot-like staining for beta-catenin on immunostaining, but no nuclear staining was observed. The patient is alive 13 months after surgery.

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胸壁硬化性上皮样纤维肉瘤
硬化性上皮样纤维肉瘤是一种罕见的纤维肉瘤变体,在高度硬化的胶原基质背景下,上皮样细胞呈股状和巢状排列。尽管肿瘤的外观相对平淡,有丝分裂活性低,但它有局部复发和远处转移的能力。我们报告一个26岁男性的胸壁硬化上皮样纤维肉瘤病例。显微镜下,肿瘤显示圆形、卵圆形或成角状的肿瘤细胞在硬化的胶原间质中增生。肿瘤细胞小至中等大小,有淡色嗜酸性细胞质,呈索状、股状和簇状排列。免疫组化结果显示,肿瘤细胞呈弥漫性波形蛋白阳性,泛细胞角蛋白、S100蛋白、人黑色素瘤黑45、CD34、平滑肌肌动蛋白和desmin阴性。肿瘤细胞免疫染色显示β -连环蛋白的核旁点样染色,未见细胞核染色。手术后患者存活了13个月。
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