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2019, Número 1

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Ann Hepatol 2019; 18 (1)


Type II Abernethy Malformation in a Patient with Primary Budd-Chiari Syndrome

Ding Peng-Xu, Han Xin-Wei, Liu C

Idioma: Ingles.
Referencias bibliográficas: 12
Paginas: 246-249
Archivo PDF: 419.30 Kb.


RESUMEN

Sin resumen.


REFERENCIAS (EN ESTE ARTÍCULO)

  1. Tripathi D, Sunderraj L, Vemala V, Mehrzad H, Zia Z, Mangat K, West R, et al. Long-term outcomes following percutaneous hepatic vein recanalization for Budd-Chiari syndrome. Liver Int 2017; 37: 111-20.

  2. Wang ZG, Jones RS. Budd-Chiari syndrome. Curr Probl Surg 1996; 33: 83-211.

  3. Mahmoud AE, Wilde JT, Elias E. Budd-Chiari syndrome and factor V Leiden mutation. Lancet 1995; 345: 526.

  4. Howard ER, Davenport M. Congenital extrahepatic portocaval shunts—the Abernethy malformation. J Pediatr Surg 1997; 32: 494-7.

  5. Morgan G, Superina R. Congenital absence of the portal vein: two cases and a proposed classification system for portasystemic vascular anomalies. J Pediatr Surg 1994; 29: 1239-41.

  6. Kopec J, Krzanowski M, Krolczyk J, Jaworek-Troc J, Krzanowska K, Sulowicz W. Abernethy malformation type I (congenital absence of the portal vein) in a patient with chronic kidney disease. Pol Arch Med Wewn 2016; 126: 1012-3.

  7. Huang Q, Shen B, Zhang Q, Xu H, Zu M, Gu Y, Wei N, et al. Comparison of Long-Term Outcomes of Endovascular Management for Membranous and Segmental Inferior Vena Cava Obstruction in Patients With Primary Budd-Chiari Syndrome. Circ Cardiovasc Interv 2016; 9: e003104.

  8. Ding PX, Li Z, Zhang SJ, Han XW, Wu Y, Wang ZG, Fu MT. Outcome of the Z-expandable metallic stent for Budd-Chiari syndrome and segmental obstruction of the inferior vena cava. Eur J Gastroenterol Hepatol 2016; 28: 972-9.

  9. Sanada Y, Urahashi T, Ihara Y, Wakiya T, Okada N, Yamada N, Egami S, et al. The role of operative intervention in management of congenital extrahepatic portosystemic shunt. Surgery 2012; 151: 404-11.

  10. Franchi-Abella S, Branchereau S, Lambert V, Fabre M, Steimberg C, Losay J, Riou JY, et al. Complications of congenital portosystemic shunts in children: therapeutic options and outcomes. J Pediatr Gastroenterol Nutr 2010; 51: 322-30.

  11. Kraus C, Sheynzon V, Hanna R, Weintraub J. Single Stage Endovascular Treatment of a Type 2 Abernethy Malformation: Successful Nonsurgical Outcome in a Case Report. Case Rep Radiol 2015; 2015: 491867.

  12. Kuo MD, Miller FJ, Lavine JE, Peterson M, Finch M. Exploiting phenotypic plasticity for the treatment of hepatopulmonary shunting in Abernethy malformation. J Vasc Interv Radiol 2010; 21: 917-22.




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