PAPPENHEIMER A M, CHEEVER F S, SALK H
J Exp Med. 1955 Feb 1;101(2):119-28. doi: 10.1084/jem.101.2.119.
There has been described a previously unrecognized disease of mice, characterized by progressive jaundice, first appearing during the nursing period. This has been shown to be due to congenital absence of the terminal segment of the common bile duct, or to the absence of intrahepatic ducts. In the former case, there is distension of the cystic and hepatic ducts, and of the gall bladder, with mucoid material. Biliary cirrhosis and infarct-like areas of necrosis are commonly found in the liver. The cause of the necroses has not been positively determined, but it is suggested that they result from defective arteriolization of the hepatic parenchyma. Inflammatory lesions of the biliary passages, when present, are attributed to secondary bacterial infection. Protozoan-like parasites were present in the gastric epithelium of all mice examined. Their relationship to the biliary and hepatic lesions is as yet undetermined.
曾描述过一种先前未被认识的小鼠疾病,其特征为进行性黄疸,最早出现在哺乳期。已表明这是由于胆总管终末段先天性缺失,或肝内胆管缺失所致。在前一种情况下,胆囊管、肝管和胆囊会因黏液样物质而扩张。肝脏中常见胆汁性肝硬化和梗死样坏死区域。坏死的原因尚未明确确定,但有人认为它们是由肝实质动脉化缺陷导致的。胆管的炎性病变(若存在)归因于继发性细菌感染。在所有检查的小鼠胃上皮中都存在类似原生动物的寄生虫。它们与胆管和肝脏病变的关系尚未确定。