在英国皇家外科学院的大鼠中,自发性胆管纤维化邻近扩张的胆总管伴肠化生。

IF 0.9 4区 医学 Q4 PATHOLOGY Journal of Toxicologic Pathology Pub Date : 2021-10-01 Epub Date: 2021-07-17 DOI:10.1293/tox.2021-0032
Kiyokazu Ozaki, Yui Terayama, Tetsuro Matsuura
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引用次数: 1

摘要

在一项长期的动物研究中,一只130周龄的雄性皇家外科学院大鼠作为未治疗的动物,在肝门静脉区出现了一个肿块,粘附在扩张的胆总管和十二指肠上。组织病理学上,孤立肿块呈扩张性生长,无明显压迫,并继续扩张胆总管,胆总管上皮增生伴肠化生。肿块主要由小到大的扩张和/或弯曲的导管组成,伴有丰富的致密结缔组织和许多炎症细胞。导管单层上皮由立方体变为柱状。免疫组化结果显示,衬里细胞角蛋白7、角蛋白19和OV-6呈阳性,这是胆管标志物。根据病理特点,诊断为自发性胆管纤维化伴胆总管扩张伴肠化生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Spontaneous cholangiofibrosis adjacent to a dilated common bile duct with intestinal metaplasia in a Royal College of Surgeons rat.

A 130-week-old male Royal College of Surgeons rat kept as a non-treated animal in a long-term animal study presented with a mass in the hepatic portal region that adhered to a dilated common bile duct and the duodenum. Histopathologically, the solitary mass showed expansive growth with no apparent compression and continued to dilate the common bile duct, which had a hyperplastic epithelium with intestinal metaplasia. The mass mainly consisted of small to large dilated and/or tortuous ducts with abundant dense connective tissue and many inflammatory cells. The single-layer lining epithelium of the duct changed from cuboidal to columnar. Immunohistochemically, the lining cells were positive for cytokeratin 7, cytokeratin 19, and OV-6, which are bile duct markers. Based on the pathological characteristics, the rat was diagnosed as spontaneous cholangiofibrosis adjacent to a dilated common bile duct with intestinal metaplasia.

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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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