Literature DB >> 26191808

New type of asymptomatic congenital portosystemic shunt.

Gabriele Bazzocchi1, Daniela Pastorelli2, Fabia Laviani2, Giovanni Simonetti2.   

Abstract

Congenital extrahepatic portosystemic shunt (CEPS) is an extremely rare anomaly. In these malformations splanchnic blood bypasses the liver and drains into the systemic circulation through the inferior vena cava (IVC) or the left renal vein (LRV). Extrahepatic shunts may be divided into type 1 [end-to-side mesenterico-caval fistula with congenital absence of the portal vein (PV)] and type 2 (partial portocaval shunt caused by side-to-side mesenterico-caval fistula with normal or hypoplasic PV). Type 2 shunts typically are wholly extrahepatic between the PV or its right branch and the retrohepatic IVC. This report describes an asymptomatic case of CEPS not previously documented and not classifiable as type 1 or 2. CT revealed a normal PV with communication between the inferior mesenteric vein (IMV) and the LRV. The inferior mesenteric vein appeared tortuous, abnormally long and with a large calibre, and presented a connection with the LRV, in addition to a normal confluence into the splenic vein. Colour Doppler revealed hepatopetal normal flow in the PV and superior mesenteric vein with mild portal hypertension and an inversion of flow in the IMV directed to the LRV. Biochemical parameters showed a normal liver function without hyperammonaemia.

Entities:  

Keywords:  Abernethy malformation; Computed tomography; Congenital extrahepatic portosystemic shunt; Portal hypertension

Year:  2008        PMID: 26191808     DOI: 10.1007/s12328-008-0037-9

Source DB:  PubMed          Journal:  Clin J Gastroenterol        ISSN: 1865-7265


  9 in total

1.  Congenital extrahepatic portocaval shunt (Abernethy type 2), huge liver mass, and patent ductus arteriosus--a case report of its rare clinical presentation in a young girl.

Authors:  Yutaka Kanamori; Kohei Hashizume; Yoshihiro Kitano; Masahiko Sugiyama; Toru Motoi; Tsuyoshi Tange
Journal:  J Pediatr Surg       Date:  2003-04       Impact factor: 2.545

2.  Ultrastructural analysis of the liver with portal vein agenesis: a case report.

Authors:  G Altavilla; P Cusatelli
Journal:  Ultrastruct Pathol       Date:  1998 Nov-Dec       Impact factor: 1.094

3.  Three brothers with progressive hepatic dysfunction and severe hepatic steatosis due to a patent ductus venosus.

Authors:  T Uchino; F Endo; S Ikeda; K Shiraki; Y Sera; I Matsuda
Journal:  Gastroenterology       Date:  1996-06       Impact factor: 22.682

Review 4.  Congenital absence of the portal vein: two cases and a proposed classification system for portasystemic vascular anomalies.

Authors:  G Morgan; R Superina
Journal:  J Pediatr Surg       Date:  1994-09       Impact factor: 2.545

5.  Distal splenorenal shunt versus transjugular intrahepatic portal systematic shunt for variceal bleeding: a randomized trial.

Authors:  J Michael Henderson; Thomas D Boyer; Michael H Kutner; John R Galloway; Layton F Rikkers; Lennox J Jeffers; Kareem Abu-Elmagd; Jason Connor
Journal:  Gastroenterology       Date:  2006-05       Impact factor: 22.682

6.  Surgical shunts and TIPS for variceal decompression in the 1990s.

Authors:  J M Henderson; A Nagle; S Curtas; M Geisinger; D Barnes
Journal:  Surgery       Date:  2000-10       Impact factor: 3.982

7.  Embolization of the left portal vein to inferior vena cava shunts for chronic recurrent hepatic encephalopathy via the mesenteric vein.

Authors:  Y Takayama; S Moriura; J Nagata; A Akutagawa; A Hirano; S Ishiguro; T Matsumoto; T Sato
Journal:  J Gastroenterol Hepatol       Date:  2001-12       Impact factor: 4.029

Review 8.  The clinical anatomy of congenital portosystemic venous shunts.

Authors:  Mark D Stringer
Journal:  Clin Anat       Date:  2008-03       Impact factor: 2.414

9.  Abernethy malformation: one of the etiologies of hepatopulmonary syndrome.

Authors:  Alfonso E Alvarez; Antônio F Ribeiro; Gabriel Hessel; Jamal Baracat; José D Ribeiro
Journal:  Pediatr Pulmonol       Date:  2002-11
  9 in total

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