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肝外门静脉性胆病:基于解剖和临床特征提出的病因学。

Extrahepatic portal biliopathy: proposed etiology on the basis of anatomic and clinical features.

机构信息

Department of Radiology, Mayo Clinic, 4500 San Pablo Dr, Jacksonville, FL 32224, USA.

出版信息

Radiology. 2011 Jan;258(1):146-53. doi: 10.1148/radiol.10090923. Epub 2010 Nov 2.

Abstract

PURPOSE

To compare the anatomic and clinical features in patients with chronic portal vein thrombosis (PVT) to determine why some patients develop portal biliopathy (PB) while most do not and propose an etiology for PB.

MATERIALS AND METHODS

This project satisfied HIPAA regulations and received institutional review board approval for a retrospective review without the need for consent. From 100 patients with PVT, 60 were extracted who had chronic, nonmalignant PVT, after exclusion of those with sclerosing cholangitis, liver transplants, choledocholithiasis, or portosystemic shunts. Clinical and imaging data from 19 patients with biliary dilatation (PB group) were compared with data from 41 patients without biliary dilatation (no-PB group). Statistical analysis was performed with the Fisher exact test for categorical variables or the Wilcoxon rank-sum test for numerical and ordered categorical variables. P values of .05 or less were considered to indicate a significant difference.

RESULTS

The etiology of PVT differed between the groups (P < .001); cirrhosis was infrequently seen in the PB group (two of 19, 11%) but was common in the no-PB group (31 of 41, 76%). Only two of 33 (6%) patients with cirrhosis and PVT had PB. Extension of PVT into the mesenteric veins was significantly more common in the PB group (18 of 19, 95%) than in the no-PB group (one of 41, 2%) (P < .001). Compared with the no-PB group, patients in the PB group had more acute angulation of the bile duct (median, 110° vs 128°; P = .008), less frequent gastroesophageal varices (three of 19 [16%] vs 20 of 41 [49%], P = .021), and a smaller mean coronary vein diameter (median, 5 vs 6 mm; P = .014).

CONCLUSION

Noncirrhotic patients with hypercoagulable states tend to develop PB when PVT extends to the splenomesenteric veins. A possible etiology is the formation of specific peribiliary venous pathways responsible for bile duct compression and tethering.

摘要

目的

比较慢性门静脉血栓形成(PVT)患者的解剖学和临床特征,以确定为什么有些患者会发生门静脉性胆病(PB),而大多数患者则不会,并提出 PB 的病因。

材料和方法

本项目符合 HIPAA 法规,并获得机构审查委员会批准进行回顾性审查,无需同意。从 100 例 PVT 患者中,排除患有硬化性胆管炎、肝移植、胆总管结石或门体分流的患者后,提取 60 例慢性非恶性 PVT 患者。将 19 例有胆管扩张的患者(PB 组)的临床和影像学数据与 41 例无胆管扩张的患者(无-PB 组)的数据进行比较。对于分类变量,采用 Fisher 确切检验进行统计学分析;对于数值和有序分类变量,采用 Wilcoxon 秩和检验。P 值小于或等于 0.05 被认为具有统计学意义。

结果

两组患者的 PVT 病因不同(P < 0.001);PB 组肝硬化少见(19 例中有 2 例,11%),无-PB 组肝硬化常见(41 例中有 31 例,76%)。仅 33 例(6%)肝硬化合并 PVT 患者有 PB。PB 组 PVT 延伸至肠系膜静脉更为常见(19 例中有 18 例,95%),无-PB 组(41 例中有 1 例,2%)(P < 0.001)。与无-PB 组相比,PB 组患者胆管锐角更明显(中位数,110°对 128°;P =.008),胃食管静脉曲张少见(19 例中有 3 例[16%],41 例中有 20 例[49%],P =.021),门静脉直径更小(中位数,5 对 6 mm;P =.014)。

结论

非肝硬化、高凝状态患者当 PVT 延伸至脾肠系膜静脉时,易发生 PB。可能的病因是形成特定的胆管周围静脉通路,导致胆管受压和束缚。

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