Service de Pédiatrie, Hôpital de Saint Etienne, Saint-Etienne, France.
Centre de Référence des Maladies Rénales Rares, Hôpital Femme Mère Enfant, 59 Boulevard Pinel, 69677, Bron, France.
Pediatr Nephrol. 2019 Jul;34(7):1289-1293. doi: 10.1007/s00467-019-04234-6. Epub 2019 Apr 8.
Liver lesions of hemolytic uremic syndrome due to Shiga-toxin-producing Escherichia coli (STEC-HUS) are uncommon.
CASE-DIAGNOSIS/TREATMENT: We report three observations of severe STEC-HUS with delayed hepatic involvement. They presented with multiple organ failure and received eculizumab; 15 days after the onset of STEC-HUS, cholestasis appeared and cytolysis worsened. Abdominal ultrasonography showed vesicular sludge. Liver biopsy performed 3 to 6 months after the STEC-HUS found cholangiolar proliferation and inflammatory portal fibrosis. Despite renal recovery, cholestasis persisted and worsened in two cases, leading to biliary cirrhosis and subsequent liver transplantation. Pathological examination of one native liver found thrombotic microangiopathy.
Even though the pathological examination performed on one native liver demonstrated areas of thrombotic microangiopathy, we cannot completely rule out that eculizumab may have worsened the liver lesions. Before the efficacy of eculizumab in STEC-HUS is formally demonstrated, physicians should stay cautious in its use.
产志贺毒素大肠杆菌(STEC-HUS)引起的溶血尿毒综合征的肝脏病变并不常见。
病例诊断/治疗:我们报告了三例严重 STEC-HUS 伴有延迟性肝受累的观察结果。它们表现为多器官衰竭并接受了依库珠单抗治疗;在 STEC-HUS 发病后 15 天,出现胆汁淤积和细胞溶解加重。腹部超声显示胆囊泥砂样。在 STEC-HUS 发生后 3 至 6 个月进行的肝活检发现胆管增生和炎症性门脉纤维化。尽管肾功能恢复,但在两例中,胆汁淤积持续存在并恶化,导致胆汁性肝硬化和随后的肝移植。对一个原肝的病理检查发现血栓性微血管病。
尽管对一个原肝的病理检查显示存在血栓性微血管病区域,但我们不能完全排除依库珠单抗可能加重了肝脏病变。在依库珠单抗在 STEC-HUS 中的疗效得到正式证实之前,医生应谨慎使用。