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原发性胆汁性肝硬化中赫林管的破坏。

Destruction of canals of Hering in primary biliary cirrhosis.

作者信息

Saxena Romil, Hytiroglou Prodromos, Thung Swan N, Theise Neil D

机构信息

Lillian and Henry M. Stratton-Hans Popper Department of Pathology, Mount Sinai School of Medicine, New York, NY, USA.

出版信息

Hum Pathol. 2002 Oct;33(10):983-8. doi: 10.1053/hupa.2002.128060.

Abstract

The canals of Hering (CoH), converging from the hepatic lobule onto the portal tract, connect bile canaliculi to the interlobular bile ducts, and represent the most proximal portion of the bile drainage pathway with a cholangiocyte lining. In this study we sought to ascertain whether this proximal pathway is involved by the disease process in primary biliary cirrhosis (PBC), which uniformly affects small bile ducts while sparing medium- and large-sized ducts. Ten biopsy specimens with early-stage PBC were compared with 6 normal control livers. Adjacent 4-micron-thick sections of routinely processed, formalin-fixed tissue were immunostained for CK19 and HLA-DR. Each terminal portal tract was assigned a stage: 0, normal; 1, bile duct damage or loss; 2, bile ductular proliferation; or 3, periportal fibrosis. The ratio of the number of CoH to number of portal tracts (i.e., the c/p ratio) was calculated for the control biopsies and individual portal tracts at each stage of PBC. The numbers of CoH were decreased in all stages of PBC (P <0.0001), with the fewest found around portal tracts at stages 0 and 1 and the most around portal tracts at stages 2 and 3, but never at normal levels. HLA-DR was expressed focally on bile ducts and CoH in PBC, but was absent in normal controls. We conclude that CoH are destroyed in PBC in concert with the destruction of small bile ducts. This destruction appears to be an early event, because CoH numbers are lowest around stage 0 portal tracts, which still contain normal bile ducts.

摘要

赫林管(CoH)从肝小叶汇聚至门管区,将胆小管与小叶间胆管相连,是胆汁引流途径中最靠近近端且内衬胆管细胞的部分。在本研究中,我们试图确定这条近端途径是否参与原发性胆汁性肝硬化(PBC)的疾病进程,PBC一致地影响小胆管,而中、大胆管不受影响。将10例早期PBC活检标本与6例正常对照肝脏进行比较。对常规处理的福尔马林固定组织的相邻4微米厚切片进行CK19和HLA-DR免疫染色。每个终末门管区被指定一个阶段:0,正常;1,胆管损伤或缺失;2,胆管增生;或3,门周纤维化。计算对照活检标本以及PBC各阶段单个门管区的赫林管数量与门管区数量之比(即c/p比)。PBC各阶段的赫林管数量均减少(P<0.0001),在0期和1期门管区周围发现的赫林管最少,在2期和3期门管区周围最多,但从未达到正常水平。HLA-DR在PBC的胆管和赫林管上呈局灶性表达,但在正常对照中不存在。我们得出结论,在PBC中,赫林管与小胆管的破坏同时发生。这种破坏似乎是一个早期事件,因为在0期门管区周围赫林管数量最少,而这些门管区仍含有正常胆管。

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