Literature DB >> 16388937

[Idiopathic intrahepatic portosytemic shunts in 4 children].

F Rouveyrol1, M Meyer, J R Lusson, C Dauphin, P Vanlieferinghen, P Déchelotte, H Laurichesse, L Guibaud, P Pracros, D Campagne, F Gaspard, A Lachaux, J-L Stéphan.   

Abstract

Intrahepatic portosystemic anastomoses are macroscopic communications between the venous portal system and the systemic circulation and located partly in the liver. We report 4 new cases of type II shunts, which illustrate the circumstances of the diagnosis of these exceptional anomalies. For 2 children, the diagnosis was done antenataly by US and spontaneous involution in a few months was observed. In the third case the malformation was evidenced fortuitously at 3 weeks of life, and this 6-year-old child remains completely asymptomatic so far. Then, in the fourth case, a cerebral venous thrombosis was fortuitously and antenatally evidenced in an otherwise uneventful pregnancy and portosystemic shunt was demonstrated postnataly in the extensive work up of the neonate.

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Year:  2006        PMID: 16388937     DOI: 10.1016/j.arcped.2005.11.013

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  1 in total

1.  Congenital portosystemic shunts and AMPLATZER vascular plug occlusion in newborns.

Authors:  William N Evans; Alvaro Galindo; Ruben J Acherman; Abraham Rothman; Dean P Berthoty
Journal:  Pediatr Cardiol       Date:  2009-07-23       Impact factor: 1.655

  1 in total

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