Pyrrolizidine alkaloids-induced hepatic sinusoidal obstruction syndrome: Pathogenesis, clinical manifestations, diagnosis, treatment, and outcomes

World J Gastroenterol. 2019 Jul 28;25(28):3753-3763. doi: 10.3748/wjg.v25.i28.3753.

Abstract

Hepatic sinusoidal obstruction syndrome (HSOS) can be caused by the intake of pyrrolizidine alkaloids (PAs). To date, PAs-induced HSOS has not been extensively studied. In view of the difference in etiology of HSOS between the West and China, clinical profiles, imaging findings, treatment, and outcomes of HSOS associated with hematopoietic stem cell transplantation or oxaliplatin might be hardly extrapolated to PAs-induced HSOS. Reactive metabolites derived from PAs form pyrrole-protein adducts that result in toxic destruction of hepatic sinusoidal endothelial cells. PAs-induced HSOS typically manifests as painful hepatomegaly, ascites, and jaundice. Laboratory tests revealed abnormal liver function tests were observed in most of the patients with PAs-induced HSOS. In addition, contrast computed tomography and magnetic resonance imaging scan show that patients with PAs-induced HSOS have distinct imaging features, which reveal that radiological imaging provides an effective noninvasive method for the diagnosis of PAs-induced HSOS. Liver biopsy and histological examination showed that PAs-induced HSOS displayed distinct features in acute and chronic stages. Therapeutic strategies for PAs-induced HSOS include rigorous fluid management, anticoagulant therapy, glucocorticoids, transjugular intrahepatic portosystemic shunt, liver transplantation, etc. The aim of this review is to describe the pathogenesis, clinical profiles, diagnostic criteria, treatment, and outcomes of PAs-induced HSOS.

Keywords: Anticoagulant therapy; Diagnostic criteria; Hepatic sinusoidal endothelial cells; Hepatic sinusoidal obstruction syndrome; Pyrrole-protein adducts; Pyrrolizidine alkaloids; Symptomatic treatment.

Publication types

  • Review

MeSH terms

  • Anticoagulants / therapeutic use
  • Biopsy
  • China
  • Endothelial Cells / pathology
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / pathology
  • Fluid Therapy / methods
  • Glucocorticoids
  • Hepatic Veins / cytology
  • Hepatic Veins / diagnostic imaging
  • Hepatic Veins / pathology*
  • Hepatic Veno-Occlusive Disease / chemically induced
  • Hepatic Veno-Occlusive Disease / diagnosis*
  • Hepatic Veno-Occlusive Disease / therapy
  • Humans
  • Liver / blood supply
  • Liver / diagnostic imaging
  • Liver / pathology
  • Liver Function Tests
  • Liver Transplantation
  • Magnetic Resonance Imaging
  • Plants, Edible / chemistry
  • Plants, Edible / toxicity*
  • Portasystemic Shunt, Transjugular Intrahepatic
  • Pyrrolizidine Alkaloids / toxicity*
  • Tomography, X-Ray Computed
  • Treatment Outcome

Substances

  • Anticoagulants
  • Glucocorticoids
  • Pyrrolizidine Alkaloids