Rastogi Archana, Bihari Chhagan, Thapar Shalini L, Bhatia Vikram
Departments of Pathology Radiodiagnosis Hepatology, Institute of Liver and Biliary Sciences, D1, Vasant Kunj, New Delhi 110070, India.
Diagnostics (Basel). 2023 Jan 25;13(3):436. doi: 10.3390/diagnostics13030436.
Portal cavernoma cholangiopathy (PCC)' refers to abnormalities of the extrahepatic and intrahepatic bile ducts in patients with portal hypertension. Although there is data on clinical and imaging aspects of PCC, the description of liver pathology has been strikingly deficient. The purpose of this study was to examine the histopathological characteristics of PCC.
A retrospective study of patients clinically diagnosed with extrahepatic portal vein obstruction (EHPVO) with portal cavernoma cholangiopathy, was conducted. Vascular anatomy was characterized by computerized tomographic angiography, and endoscopic retrograde cholangiography (ERC) and magnetic resonance cholangiography (MRC) were used to characterize the biliary anatomy. Histological features were analyzed by two hepatopathologists in a blinded manner, with mutual discussion to resolve any discrepancies.
A total of 50 patients with portal cavernoma cholangiopathy were included in the study. The mean age of the patients was 26.2 ± 11.6 years. Radiologically, bilobar intrahepatic biliary dilatation was seen in 98% with common bile duct abnormality in 100% of patients, along with extrinsic ductal impressions in 77 % of cases. Liver tests were deranged total bilirubin 1.5 mg/dL (IQR 0.8-2.4) and alkaline phosphatase 109.5 IU/L (IQR 70-193). Histologically; dilated multiple portal venous channels (72%), hepatic artery thickening (70%). The presence of aberrant vascular channels around portal tracts (54%), elastosis of portal veins (50%), and bile ductular reaction in (44%) were the other prominent findings. A 12% of cases show focal thin bridges. Advanced fibrosis was not seen in any of the cases. One-fourth of the cases showed concomitant minimal to mild hepatocyte steatosis.
Histologically, intrahepatic portal vein and portal tract abnormalities were noted in cases with portal cavernoma cholangiopathy, associated with mild derangement of liver tests.
门静脉海绵样变性胆管病(PCC)是指门静脉高压患者肝外和肝内胆管的异常。尽管有关于PCC临床和影像学方面的数据,但肝脏病理学描述却极为欠缺。本研究旨在探讨PCC的组织病理学特征。
对临床诊断为肝外门静脉阻塞(EHPVO)伴门静脉海绵样变性胆管病的患者进行回顾性研究。通过计算机断层血管造影术对血管解剖结构进行特征分析,采用内镜逆行胆管造影术(ERC)和磁共振胆管造影术(MRC)对胆管解剖结构进行特征分析。由两名肝脏病理学家以盲法分析组织学特征,并通过相互讨论解决任何分歧。
本研究共纳入50例门静脉海绵样变性胆管病患者。患者的平均年龄为26.2±11.6岁。影像学上,98%的患者出现双叶肝内胆管扩张,100%的患者胆总管异常,77%的病例存在外在胆管压迹。肝功能检查异常,总胆红素为1.5mg/dL(四分位间距0.8 - 2.4),碱性磷酸酶为109.5IU/L(四分位间距70 - 193)。组织学上,多个门静脉通道扩张(72%),肝动脉增粗(70%)。门静脉周围存在异常血管通道(54%)、门静脉弹性组织变性(50%)以及胆管反应(44%)是其他突出发现。12%的病例显示局灶性细桥。所有病例均未发现重度纤维化。四分之一的病例伴有轻度至中度肝细胞脂肪变性。
组织学上,门静脉海绵样变性胆管病患者存在肝内门静脉和门静脉周围异常,伴有肝功能轻度异常。