Shimazaki Taishi, Yasui Yuzo, Anagawa-Nakamura Akiko, Toyoda Kaoru, Yamazaki Ryo, Onami Saeko, Kemmochi Yusuke, Shoda Toshiyuki
Toxicology Research Laboratories, Yokohama Research Center, Central Pharmaceutical Research Institute, Japan Tobacco Inc., 1-13-2 Fukuura, Kanazawa-ku, Yokohama, Kanagawa 236-0004, Japan.
Scientific Product Assessment Center, R and D Group, Japan Tobacco Inc., 6-2 Umegaoka, Aoba-ku, Yokohama, Kanagawa 227-8512, Japan.
J Toxicol Pathol. 2024 Jul;37(3):133-137. doi: 10.1293/tox.2024-0022. Epub 2024 May 8.
We report a histiocytic sarcoma originating from the epididymis observed in a 110-week-old male CD-1 mouse in a carcinogenicity study. At necropsy, no lesions were observed in the epididymis. Histologically, a neoplastic lesion was observed in the cauda of the epididymis that was well demarcated from the surrounding tissues. The lesion mainly consisted of spindle-shaped tumor cells with oval to elongated nuclei and abundant eosinophilic or foamy cytoplasm. The tumor cells were arranged in a fascicular pattern, interlacing bundles, or a whorl pattern. The nuclei showed mild atypia with irregular shapes and varied sizes, whereas few mitotic figures and no typical multinucleated cells were observed. The epididymal ducts remained within the neoplastic lesion, and the tumor cells invaded between the epithelium and the smooth muscle layer of the epididymal duct. Immunohistochemically, the tumor cells were positive for vimentin and macrophage markers (Iba1, CD204, F4/80, and Mac-2) but negative for cytokeratin and other mesenchymal cell (α-smooth muscle actin, desmin, CD31, and platelet-derived growth factor receptor-β), neural cell (S-100 and nestin), or Leydig cell markers (calretinin). Proliferating cell nuclear antigen-positive tumor cells were sporadically observed in the lesion. Based on these results, the tumor was diagnosed as a histiocytic sarcoma originating from the epididymis. This report provides additional histopathological evidence of spontaneous histiocytic sarcomas originating from the epididymis of aged mice.
我们报告了在一项致癌性研究中,一只110周龄雄性CD-1小鼠发生的起源于附睾的组织细胞肉瘤。尸检时,附睾未观察到病变。组织学上,在附睾尾部观察到一个肿瘤性病变,与周围组织界限清楚。病变主要由梭形肿瘤细胞组成,细胞核呈椭圆形至细长形,细胞质丰富,呈嗜酸性或泡沫状。肿瘤细胞呈束状、交错束状或漩涡状排列。细胞核显示轻度异型性,形状不规则,大小不一,而仅见少数有丝分裂象,未观察到典型的多核细胞。附睾管保留在肿瘤性病变内,肿瘤细胞侵入附睾管上皮和平滑肌层之间。免疫组化显示,肿瘤细胞波形蛋白和巨噬细胞标志物(Iba1、CD204、F4/80和Mac-2)呈阳性,但细胞角蛋白和其他间充质细胞(α-平滑肌肌动蛋白、结蛋白、CD31和血小板衍生生长因子受体-β)、神经细胞(S-100和巢蛋白)或睾丸间质细胞标志物(钙视网膜蛋白)呈阴性。病变中偶尔可见增殖细胞核抗原阳性的肿瘤细胞。基于这些结果,该肿瘤被诊断为起源于附睾的组织细胞肉瘤。本报告提供了老年小鼠附睾自发组织细胞肉瘤的额外组织病理学证据。