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首页> 外文期刊>Histopathology: Official Journal of the British Division of the International Academy of Pathology >Inflammatory disease of the bile ducts-cholangiopathies: Liver biopsy challenge and clinicopathological correlation
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Inflammatory disease of the bile ducts-cholangiopathies: Liver biopsy challenge and clinicopathological correlation

机译:胆管炎-胆管疾病:肝活检的挑战和临床病理相关性

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摘要

Liver biopsy challenge and clinicopathological correlation Liver biopsy interpretation in inflammatory diseases of the bile ducts or chronic cholangiopathies may be challenging, especially for pathologists working outside referral centres, where there is a limited exposure to relatively uncommon conditions. In view of the importance of sampling errors resulting from the patchy distribution of pathognomonic bile duct injuries and the misleading absence of cholestasis in the early stages, there is a need to recognize surrogate markers and subtle changes, in particular the early periportal deposition of copper and mild biliary interface activity. Such findings may either constitute the first indication of a primarily biliary disorder or be supportive of a clinically suspected diagnosis. Histological changes common to chronic cholangiopathies are reviewed at the variable stages of development that patients may first present to clinicians. As awareness of the protean clinical manifestations is essential for histological interpretation, the major and distinctive anatomoclinical features of primary biliary cirrhosis and primary and acquired sclerosing cholangitis are revisited, together with so-called overlapping syndromes and less common variants and associations, including more recently documented conditions, such as IgG4-related disease and the rarer multidrug resistance 3 deficiency. The review stresses the importance of evaluating histological changes in conjunction with clinical information.
机译:肝活检的挑战和临床病理相关性胆管炎或慢性胆管疾病的肝活检解释可能具有挑战性,特别是对于在转诊中心以外工作的病理学家而言,那里的感染相对较少见。鉴于在早期阶段由致病性胆管损伤的不规则分布和胆汁淤积的误导性缺失引起的采样误差的重要性,有必要认识到替代标志物和细微变化,尤其是铜和铜的早期门静脉沉积。轻度胆道界面活动。这些发现可能构成了原发性胆道疾病的最初指征,也可能支持临床上可疑的诊断。在患者可能首先呈现给临床医生的不同发育阶段,对慢性胆管病常见的组织学变化进行了回顾。由于认识到蛋白质的临床表现对于组织学解释至关重要,因此将重新探讨原发性胆汁性肝硬化,原发性和获得性硬化性胆管炎的主要和独特的解剖临床特征,以及所谓的重叠综合征和较不常见的变异和关联,包括最近文献报道。疾病,例如IgG4相关疾病和罕见的多药耐药性3缺乏症。该评论强调了结合临床信息评估组织学变化的重要性。

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