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Sinusoidal obstruction syndrome (hepatic veno-occlusive disease)
Cathy Q Fan1, James M Crawford1
1Hofstra North Shore-LIJ School of Medicine, North Shore-LIJ Health System, Manhasset, NY, USA.
Insights
Hepatic sinusoidal obstruction syndrome (SOS), or veno-occlusive disease (VOD), is a severe liver condition often linked to medical treatments. Early diagnosis and management are crucial for patient outcomes.
Area of Science:
- Hepatology
- Oncology
- Transplantation Medicine
Background:
- Hepatic sinusoidal obstruction syndrome (SOS), also known as veno-occlusive disease (VOD), is a serious complication following certain medical treatments.
- It involves damage to liver sinusoidal endothelial cells (SEC) leading to venule occlusion and potential mortality.
Purpose of the Study:
- To review the pathogenesis, clinical presentation, diagnosis, treatment, and prevention strategies for hepatic sinusoidal obstruction syndrome.
- To highlight the critical nature of SOS and the need for comprehensive management.
Main Methods:
- Literature review of pathogenesis, clinical manifestations, diagnostic approaches, and therapeutic interventions for SOS.
- Discussion of preventative measures in high-risk patient populations.
Main Results:
- SOS is associated with cytoreductive therapy for HSCT, oxaliplatin chemotherapy, and herbal remedies.
- Pathogenesis involves SEC destruction, endothelial dysfunction, and activation of clotting factors.
- Clinical signs include jaundice, hepatomegaly, ascites, and weight gain.
Conclusions:
- Transjugular liver biopsy is often preferred for diagnosis to rule out other liver conditions.
- Treatment involves fluid management, medications like defibrotide, and potentially liver transplantation.
- Prevention strategies include modified HSCT protocols, ursodeoxycholic acid, and bevacizumab in chemotherapy regimens.
Abstract:
Hepatic sinusoidal obstruction syndrome (SOS) is an obliterative venulitis of the terminal hepatic venules, which in its more severe forms imparts a high risk of mortality. SOS, also known as veno-occlusive disease (VOD), occurs as a result of cytoreductive therapy prior to hematopoietic stem cell transplantation (HSCT), following oxaliplatin-containing adjuvant or neoadjuvant chemotherapy for colorectal carcinoma metastatic to the liver and treated by partial hepatectomy, in patients taking pyrrolizidine alkaloid-containing herbal remedies, and in other particular settings such as the autosomal recessive condition of veno-occlusive disease with immunodeficiency (VODI). A central pathogenic event is toxic destruction of hepatic sinusoidal endothelial cells (SEC), with sloughing and downstream occlusion of terminal hepatic venules. Contributing factors are SEC glutathione depletion, nitric oxide depletion, increased intrahepatic expression of matrix metalloproteinases and vascular endothelial growth factor (VEGF), and activation of clotting factors. The clinical presentation of SOS includes jaundice, development of right upper-quadrant pain and tender hepatomegaly, ascites, and unexplained weight gain. Owing to the potentially critical condition of these patients, transjugular biopsy may be the preferred route for liver biopsy to exclude other potential causes of liver dysfunction and to establish a diagnosis of SOS. Treatment includes rigorous fluid management so as to avoid excessive fluid overload while avoiding too rapid diuresis or pericentesis, potential use of pharmaceutics such as defibrotide, coagulolytic agents, or methylprednisolone, and liver transplantation. Proposed strategies for prevention and prophylaxis include reduced-intensity conditioning radiation for HSCT, treatment with ursodeoxycholic acid, and inclusion of bevacizumab with oxaliplatin-based chemotherapeutic regimes. While significant progress has been made in understanding the pathogenesis of SOS and in mitigating against its adverse outcomes, this condition remains a serious complication of a selective group of medical treatments.
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