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Percutaneous mesocaval shunt creation for portal thrombosis in a patient with a JAK2V617F mutation.
Farhan, Ahmed; Liddell, Robert P.
Afiliação
  • Farhan A; Division of Interventional Radiology, Yale Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06510, USA. Electronic address: ahmed.farhan@yale.edu.
  • Liddell RP; Division of Interventional Radiology, Russell H. Morgan Department of Radiology and Radiological Sciences, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. Electronic address: rliddel1@jhmi.edu.
Thromb Res ; 234: 158-161, 2024 02.
Article em En | MEDLINE | ID: mdl-38241766
ABSTRACT
Myeloproliferative neoplasms (MPN) are the most common cause of noncirrhotic, nontumoral portal vein thrombosis (PVT). Over 90 % of MPN patients with PVT carry the JAK2V617F mutation. Compared to other etiologies of PVT, patients with JAK2V617F MPNs are at increased risk of developing significant portal hypertension. However, when these patients develop refractory portal hypertensive complications requiring portosystemic shunt placement, they have limited options. Transjugular intrahepatic portosystemic shunt (TIPS) insertion is often not feasible, as these patients tend to have extensive, occlusive portal thrombus with cavernous transformation. Surgical portosystemic shunt creation can be an alternative; however, this is associated with significant mortality. In this report, we describe the novel use of a percutaneous mesocaval shunt for successful portomesenteric decompression in a patient with portal hypertension from PVT associated with JAK2V617F positive essential thrombocythemia.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derivação Portossistêmica Transjugular Intra-Hepática / Trombose Venosa / Hipertensão Portal Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derivação Portossistêmica Transjugular Intra-Hepática / Trombose Venosa / Hipertensão Portal Idioma: En Ano de publicação: 2024 Tipo de documento: Article