4.3 Article

Noncirrhotic Portal Hypertension Current and Emerging Perspectives

期刊

CLINICS IN LIVER DISEASE
卷 23, 期 4, 页码 781-+

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.cld.2019.07.006

关键词

Idiopathic portal hypertension; Extrahepatic portal venous obstruction; Animal models; Biliopathy; Rex shunt; Parenchymal extinction

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Idiopathic portal hypertension (IPH) and extrahepatic portal venous obstruction (EHPVO) are prototype noncirrhotic causes of hypertension (PHI), characterized by normal hepatic venous pressure gradient, variceal bleeds, and moderate to massive splenomegaly with preserved liver synthetic functions. Infections, toxins, and immunologic, prothrombotic and genetic disorders are possible causes in IPH, whereas prothrombotic and local factors around the portal vein lead to EHPVO. Growth failure, portal biliopathy, and minimal hepatic encephalopathy are long-term concerns in EHPVO. Surgical shunts and transjugular intrahepatic portosystemic shunt resolve the complications secondary to PHT. Meso-Rex shunt is now the standard-of-care surgery in children with EHPVO.

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