Ludwig J, Wiesner R H, LaRusso N F
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905.
J Hepatol. 1988 Oct;7(2):193-9. doi: 10.1016/s0168-8278(88)80482-3.
We describe three adult patients who had chronic cholestatic liver disease associated with unexplained loss of interlobular bile ducts; two of these patients eventually required orthotopic liver transplantation. We have named this condition 'idiopathic adulthood ductopenia' because (1) the etiology is unknown, (2) the age of the patients may be the only distinguishing feature between this newly described condition and neonatal or infantile nonsyndromatic paucity of intrahepatic bile ducts, and (3) morphologic demonstration of ductopenia is an indispensable finding. Our three patients, all males, had a negative drug history, absence of antimitochondrial antibodies, normal cholangiographic findings, and no evidence of inflammatory bowel disease. Idiopathic adulthood ductopenia may be a representation of (1) late onset of infantile paucity of intrahepatic bile ducts, (2) destructive viral cholangitis, and (3) isolated small-duct primary sclerosing cholangitis - that is, 'pericholangitis' unassociated with inflammatory bowel disease.
我们描述了三名成年患者,他们患有慢性胆汁淤积性肝病,并伴有不明原因的小叶间胆管缺失;其中两名患者最终需要进行原位肝移植。我们将这种病症命名为“特发性成人胆管减少症”,原因如下:(1)病因不明;(2)患者年龄可能是这种新描述病症与新生儿或婴儿期非综合征性肝内胆管稀少之间唯一的区别特征;(3)胆管减少的形态学表现是一项不可或缺的发现。我们的三名患者均为男性,药物史阴性,无抗线粒体抗体,胆管造影结果正常,且无炎症性肠病的证据。特发性成人胆管减少症可能表现为:(1)婴儿期肝内胆管稀少的迟发性发作;(2)破坏性病毒性胆管炎;(3)孤立性小胆管原发性硬化性胆管炎,即与炎症性肠病无关的“胆管周围炎”。