一只老年雄性 C57BL/6J 小鼠头颅纵隔淋巴结中的自发性 B 细胞淋巴瘤

IF 0.9 4区 医学 Q4 PATHOLOGY
Shoko SUZUKI, Mao MIZUKAWA, Akane KASHIMURA, Hironobu NISHINA, Tetsuya SAKAIRI, Satomi NISHIKAWA
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引用次数: 0

摘要

B细胞淋巴瘤一般出现在老龄小鼠的脾脏、肠系膜淋巴结和派尔斑,很少出现在其他器官。在此,我们报告了一例75周大的雄性C57BL/6J小鼠颅纵隔淋巴结自发性B细胞淋巴瘤病例。从宏观上看,在心脏底部发现了一个白色肿块,与胸腺没有任何联系。显微镜检查发现,肿块中心的肿瘤细胞呈实性增生,细胞核较大。在中心和外围区域发现了一些巨噬细胞、正常大小的淋巴细胞和淋巴窦。免疫组化分析显示,分化簇 19、配对盒蛋白 5、免疫球蛋白 M 和 Ki-67 染色阳性,但细胞角蛋白 AE1/AE3 染色不阳性。这些结果与已有的小鼠淋巴瘤分类不完全一致,因此诊断为起源于颅纵隔淋巴结的B细胞淋巴瘤。本病例报告首次记录了高龄 C57BL/6J 小鼠颅纵隔淋巴结中的 B 细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spontaneous B-cell lymphoma in the cranial mediastinal lymph node of an aged male C57BL/6J mouse

B-cell lymphoma is generally observed in the spleen, mesenteric lymph nodes, and Peyer’s patches in aged mice and rarely appears in other organs. Herein, we report a case of spontaneous B-cell lymphoma originating from the cranial mediastinal lymph node in a male 75-week-old C57BL/6J mouse. Macroscopically, a white mass was found at the base of the heart with no connection to the thymus. Microscopic examination revealed a solid proliferation of tumor cells with large nuclei at the center of the mass. Some macrophages, normal-sized lymphocytes, and lymphatic sinuses were found in both central and peripheral areas. Immunohistochemical analysis showed positive staining for cluster of differentiation 19, paired box protein 5, immunoglobulin M, and Ki-67 but not for cytokeratin AE1/AE3. These findings were not completely consistent with the established mouse lymphoma classification, leading to a diagnosis of B-cell lymphoma originating from the cranial mediastinal lymph node. This case report is the first to document a B-cell lymphoma in the cranial mediastinal lymph nodes in an aged C57BL/6J mouse model.

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来源期刊
Journal of Toxicologic Pathology
Journal of Toxicologic Pathology PATHOLOGY-TOXICOLOGY
CiteScore
2.10
自引率
16.70%
发文量
22
审稿时长
>12 weeks
期刊介绍: JTP is a scientific journal that publishes original studies in the field of toxicological pathology and in a wide variety of other related fields. The main scope of the journal is listed below. Administrative Opinions of Policymakers and Regulatory Agencies Adverse Events Carcinogenesis Data of A Predominantly Negative Nature Drug-Induced Hematologic Toxicity Embryological Pathology High Throughput Pathology Historical Data of Experimental Animals Immunohistochemical Analysis Molecular Pathology Nomenclature of Lesions Non-mammal Toxicity Study Result or Lesion Induced by Chemicals of Which Names Hidden on Account of the Authors Technology and Methodology Related to Toxicological Pathology Tumor Pathology; Neoplasia and Hyperplasia Ultrastructural Analysis Use of Animal Models.
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