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成年 MDR3/ABCB4 基因突变患者的肝脏病理学特征。

Aspects of liver pathology in adult patients with MDR3/ABCB4 gene mutations.

机构信息

Service d'Anatomie Pathologique, APHP, Hôpital St Antoine, 75012 Paris, France.

出版信息

Virchows Arch. 2012 Mar;460(3):291-8. doi: 10.1007/s00428-012-1202-6. Epub 2012 Feb 14.

Abstract

The aims of this study were to describe the histological liver lesions in adult patients with MDR3/ ABCB4 mutation and to study the usefulness of MDR3 immunostaining as a diagnostic tool. All adult patients from our institution with an MDR3/ABCB4 mutation and a liver histology were included (n = 13). Eleven patients had a single heterozygous gene mutation and two patients had two heterozygous mutations. Two patients had no liver lesions. Eight patients had a mild ductular reaction and portal fibrosis. One patient had a few fibrous septa and two patients had biliary cirrhosis. In three cases intraductal lipid crystals were identified. Two patients had biliary fibroobliterative lesions with no sclerosing cholangitis on cholangiography. Biliary dysplasia was identified in hepatectomy specimens from two patients, one of whom developed an intrahepatic cholangiocarcinoma. One patient with biliary cirrhosis developed a hepatocellular carcinoma. MDR3 immunostainings performed on formalin-fixed paraffin-embedded sections showed a strong canalicular staining in all patients except in one. To conclude, the predominant histological features were ductular reaction with no or mild fibrosis without cholangitis. Liver lesions previously unreported in association with MDR3/ABCB4 gene mutations (biliary dysplasia, cholangiocarcinoma, small duct sclerosing cholangitis) were also found. Lipid crystals in bile ducts may be suggestive of MDR3/ABCB4 mutation. MDR3 immunostaining on formalin-fixed paraffin-embedded sections does not seem to be sensitive for the diagnosis of heterozygous MDR3/ABCB4 mutations.

摘要

本研究的目的是描述 MDR3/ABCB4 基因突变的成年患者的肝组织学病变,并研究 MDR3 免疫染色作为诊断工具的有用性。我们机构中所有患有 MDR3/ABCB4 突变和肝组织学的成年患者均包括在内(n=13)。11 名患者存在单一杂合基因突变,2 名患者存在两个杂合突变。2 名患者无肝病变。8 名患者存在轻微的胆管反应和门脉纤维化。1 名患者有少量纤维性间隔,2 名患者存在胆汁性肝硬化。在 3 例中发现了胆管内脂质晶体。2 名患者存在胆管纤维闭塞病变,胆管造影未见硬化性胆管炎。2 例肝切除术标本中发现胆管发育不良,其中 1 例发展为肝内胆管癌。1 例胆汁性肝硬化患者发展为肝细胞癌。对福尔马林固定石蜡包埋切片进行的 MDR3 免疫染色显示,除 1 例外,所有患者均存在强胆管染色。总之,主要的组织学特征是胆管反应,无或轻度纤维化,无胆管炎。还发现了与 MDR3/ABCB4 基因突变相关的先前未报道的肝病变(胆管发育不良、胆管癌、小胆管硬化性胆管炎)。胆管内的脂质晶体可能提示 MDR3/ABCB4 突变。福尔马林固定石蜡包埋切片上的 MDR3 免疫染色似乎对杂合 MDR3/ABCB4 突变的诊断不敏感。

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