Colantuono Rossella, Pavanello Chiara, Pietrobattista Andrea, Turri Marta, Francalanci Paola, Spada Marco, Vajro Pietro, Calabresi Laura, Mandato Claudia
Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.
Dipartimento di Scienze Farmacologiche e Biomolecolari, Centro E. Grossi Paoletti, Università degli Studi di Milano, Milan, Italy.
Front Pediatr. 2022 Aug 4;10:969081. doi: 10.3389/fped.2022.969081. eCollection 2022.
Lipoprotein X (LpX) - mediated extremely severe hyperlipidemia is a possible feature detectable in children with syndromic paucity of intralobular bile ducts (Alagille syndrome) but rarely in other types of intra- and/or extrahepatic infantile cholestasis.
Here we report on a previously well 18-month child admitted for cholestatic jaundice and moderate hepatomegaly. Laboratory tests at entry showed conjugated hyperbilirubinemia, elevated values of serum aminotransferases, gamma-glutamyl transpeptidase (GGT) and bile acids (100 folds upper normal values). Extremely severe and ever-increasing hypercholesterolemia (total cholesterol up to 1,730 mg/dl) prompted an extensive search for causes of high GGT and/or hyperlipidemic cholestasis, including an extensive genetic liver panel (negative) and a liver biopsy showing a picture of obstructive cholangitis, biliary fibrosis, and bile duct proliferation with normal MDR3 protein expression. Results of a lipid study showed elevated values of unesterified cholesterol, phospholipids, and borderline/low apolipoprotein B, and low high-density lipoprotein-cholesterol. Chromatographic analysis of plasma lipoproteins fractions isolated by analytical ultracentrifugation revealed the presence of the anomalous lipoprotein (LpX). Magnetic resonance cholangiopancreatography and percutaneous transhepatic cholangiography showed stenosis of the confluence of the bile ducts with dilation of the intrahepatic biliary tract and failure to visualize the extrahepatic biliary tract. Surgery revealed focal fibroinflammatory stenosis of the left and right bile ducts confluence, treated with resection and bilioenteric anastomosis, followed by the rapid disappearance of LpX, paralleling the normalization of serum lipids, bilirubin, and bile acids, with a progressive reduction of hepatobiliary enzymes.
We have described a unique case of focal non-neoplastic extrahepatic biliary stenosis of uncertain etiology, presenting with unusual extremely high levels of LpX-mediated hypercholesterolemia, a condition which is frequently mistaken for LDL on routine clinical tests.
脂蛋白X(LpX)介导的极重度高脂血症是小叶内胆管综合征(阿拉吉尔综合征)患儿可能出现的一种特征,但在其他类型的肝内和/或肝外婴儿胆汁淤积中很少见。
我们在此报告一名18个月大的此前健康儿童,因胆汁淤积性黄疸和中度肝肿大入院。入院时的实验室检查显示结合胆红素血症、血清转氨酶、γ-谷氨酰转肽酶(GGT)和胆汁酸值升高(高于正常值100倍)。极重度且不断升高的高胆固醇血症(总胆固醇高达1730mg/dl)促使对高GGT和/或高脂血症性胆汁淤积的病因进行广泛排查,包括广泛的基因肝脏检测(结果为阴性)以及肝脏活检,显示为阻塞性胆管炎、胆管纤维化和胆管增生,多药耐药蛋白3(MDR3)蛋白表达正常。血脂研究结果显示游离胆固醇、磷脂值升高,载脂蛋白B处于临界/低值,高密度脂蛋白胆固醇降低。通过分析超速离心分离的血浆脂蛋白组分的色谱分析显示存在异常脂蛋白(LpX)。磁共振胰胆管造影和经皮经肝胆管造影显示胆管汇合处狭窄,肝内胆管扩张,肝外胆管未显影。手术显示左右胆管汇合处存在局灶性纤维炎性狭窄,经切除和胆肠吻合术治疗,随后LpX迅速消失,同时血脂、胆红素和胆汁酸恢复正常,肝胆酶逐渐降低。
我们描述了一例病因不明的局灶性非肿瘤性肝外胆管狭窄的独特病例,其表现为异常高水平的LpX介导的高胆固醇血症,这种情况在常规临床检查中常被误诊为低密度脂蛋白。