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Hepatic veno-occlusive disease: a chemotherapy-related toxicity in children with malignancies.
- Source :
-
Paediatric drugs [Paediatr Drugs] 2010 Oct 01; Vol. 12 (5), pp. 277-84. - Publication Year :
- 2010
-
Abstract
- Hepatic veno-occlusive disease (VOD) is a major manifestation of liver toxicity associated with conventional and high-dose chemotherapy in children affected by hematologic malignancies and certain solid tumors. Clinically, patients present with jaundice, painful hepatomegaly, and fluid retention, which may evolve into multi-organ failure, a hallmark of severe disease. The pathogenesis is complex and not completely understood, but the damage to sinusoidal endothelium, typically caused by toxic metabolites released from antineoplastic drugs, is thought to play a crucial role, together with cytokine activation, immune deregulation, and coagulopathy. Diagnosis is based on clinical criteria supported by characteristic ultrasound findings, with the gold standard investigation being hepatic-venous pressure gradient measurement and biopsy. Several treatment options have been tested; the most convincing approach to date is the use of defibrotide, a novel oligonucleotide with antithrombotic and antiplatelet aggregating properties, as well as endothelial-stabilizing effects. This agent, together with other specific forms of supportive care, has shown efficacy in the treatment of established VOD and promising results in the prevention of VOD in pediatric patients receiving chemotherapy.
- Subjects :
- Animals
Antineoplastic Agents therapeutic use
Child
Hepatic Veno-Occlusive Disease diagnosis
Hepatic Veno-Occlusive Disease physiopathology
Hepatic Veno-Occlusive Disease therapy
Humans
Neoplasms complications
Prognosis
Risk Factors
Antineoplastic Agents adverse effects
Hepatic Veno-Occlusive Disease chemically induced
Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1179-2019
- Volume :
- 12
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Paediatric drugs
- Publication Type :
- Academic Journal
- Accession number :
- 20799757
- Full Text :
- https://doi.org/10.2165/11531840-000000000-00000