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Erschienen in: Pediatric Surgery International 12/2020

06.10.2020 | Technical Innovation

Laparoscopic ligation of portosystemic shunt for the treatment of congenital intrahepatic portosystemic shunt in one newborn infant

verfasst von: Jin-Shan Zhang, Long Li

Erschienen in: Pediatric Surgery International | Ausgabe 12/2020

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Abstract

Background

Congenital portosystemic shunt (CPSS) is a rare congenital portal malformation. 35.5% of CPSS is intrahepatic. Certain intrahepatic CPSS cases can be spontaneously closed within 2 years after birth. However, the intrahepatic CPSS with clinical symptoms or large shunt requires immediate treatment. In the present study, we used a laparoscopic ligation of portosystemic shunt to treat one newborn case.

Materials and methods

An abnormal shunt between the portal and the hepatic vein was initially detected by a prenatal ultrasound in one newborn infant. The postnatal ultrasound and CT indicated a connection between the left portal and hepatic vein and a venous cyst at the anterior edge of the left liver. Owing to the hyperammonemia and the large shunt from the portal into the hepatic vein, the infant was treated with a laparoscopic ligation of the shunt. During the operation, the left portal vein and its branches were dissected and the anterior branch of the left portal vein was clamped using a Hem-o-lok. The venous cyst was sutured and ligated using a prolene suture.

Results

The surgery was completed successfully. The duration of the operation time was 60 min. The postoperative hospital stay was 3 days. The preoperative portal angiography indicated an intrahepatic shunt between the left portal and the left hepatic vein and a venous cyst. Postoperative portal angiography indicated the disappearance of the abnormal shunt and the venous cyst. The portal pressure was increased from the preoperative 6 cmH2O to the postoperative 12 cmH2O. The duration of the follow-up was 22 months. Following surgery, the level of serum ammonia returned to normal. The postoperative CT demonstrated that the abnormal shunt had disappeared. No symptoms of portal hypertension were noted following surgery, such as splenomegaly, hypothrombocytopenia, and upper gastrointestinal bleeding.

Conclusion

The laparoscopic ligation of portosystemic shunt is suitable for the treatment of the intrahepatic CPSS in the newborn patient.
Literatur
1.
Zurück zum Zitat Bernard O, Franchi-Abella S, Branchereau S et al (2012) Congenital portosystemic shunts in children: recognition, evaluation, and management. Semin Liver Dis 32(4):273–287CrossRef Bernard O, Franchi-Abella S, Branchereau S et al (2012) Congenital portosystemic shunts in children: recognition, evaluation, and management. Semin Liver Dis 32(4):273–287CrossRef
2.
Zurück zum Zitat Shapiro RS, Winsberg F, Stancato-Pasik A et al (1993) Color Doppler sonography of vascular malformations of the liver. J Ultrasound Med 12(6):343–348CrossRef Shapiro RS, Winsberg F, Stancato-Pasik A et al (1993) Color Doppler sonography of vascular malformations of the liver. J Ultrasound Med 12(6):343–348CrossRef
3.
Zurück zum Zitat Gitzelmann R, Forster I, Willi UV (1997) Hypergalactosaemia in a newborn: self-limiting intrahepatic portosystemic venous shunt. Eur J Pediatr 156(9):719–722CrossRef Gitzelmann R, Forster I, Willi UV (1997) Hypergalactosaemia in a newborn: self-limiting intrahepatic portosystemic venous shunt. Eur J Pediatr 156(9):719–722CrossRef
4.
Zurück zum Zitat Ono H, Mawatari H, Mizoguchi N et al (2010) Clinical features and outcome of eight infants with intrahepatic porto-venous shunts detected in neonatal screening for galactosaemia. Acta Paediatr 87(6):631–634CrossRef Ono H, Mawatari H, Mizoguchi N et al (2010) Clinical features and outcome of eight infants with intrahepatic porto-venous shunts detected in neonatal screening for galactosaemia. Acta Paediatr 87(6):631–634CrossRef
5.
Zurück zum Zitat Chiaie DL, Neuberger P, Kalle TV (2008) Congenital intrahepatic portosystemic shunt: prenatal diagnosis and possible influence on fetal growth. Ultrasound Obstet Gynecol 32(2):233–235CrossRef Chiaie DL, Neuberger P, Kalle TV (2008) Congenital intrahepatic portosystemic shunt: prenatal diagnosis and possible influence on fetal growth. Ultrasound Obstet Gynecol 32(2):233–235CrossRef
6.
Zurück zum Zitat Sagiv-Friedgut K, Witzling M, Dalal I et al (2007) Congenital patent ductusvenosus: an association with the hyper IgE syndrome. J Pediatr 150(2):210–212CrossRef Sagiv-Friedgut K, Witzling M, Dalal I et al (2007) Congenital patent ductusvenosus: an association with the hyper IgE syndrome. J Pediatr 150(2):210–212CrossRef
7.
Zurück zum Zitat Uchino T, Endo F, Ikeda S et al (1996) Three brothers with progressive hepatic dysfunction and severe hepatic steatosis due to a patent ductus venosus. Gastroenterology 110(6):1964–1968CrossRef Uchino T, Endo F, Ikeda S et al (1996) Three brothers with progressive hepatic dysfunction and severe hepatic steatosis due to a patent ductus venosus. Gastroenterology 110(6):1964–1968CrossRef
8.
Zurück zum Zitat Noe JA, Pittman HC, Burton EM (2006) Congenital absence of the portal vein in a child with Turner syndrome. Pediatr Radiol 36(6):566–568CrossRef Noe JA, Pittman HC, Burton EM (2006) Congenital absence of the portal vein in a child with Turner syndrome. Pediatr Radiol 36(6):566–568CrossRef
9.
Zurück zum Zitat Stringer MD (2008) The clinical anatomy of congenital portosystemic venous shunts. Clin Anat 21(2):147–157CrossRef Stringer MD (2008) The clinical anatomy of congenital portosystemic venous shunts. Clin Anat 21(2):147–157CrossRef
10.
Zurück zum Zitat Murray CP, Yoo SJ, Babyn PS (2003) Congenital extrahepatic portosystemic shunts. Pediatr Radiol 33(9):614–620CrossRef Murray CP, Yoo SJ, Babyn PS (2003) Congenital extrahepatic portosystemic shunts. Pediatr Radiol 33(9):614–620CrossRef
11.
Zurück zum Zitat Kieran MW, Vekemans M, Robb LJ et al (1992) Portohepatic shunt in a Down syndrome patient with an interchange trisomy 47, XY,-2,+der(2), +der(21)t(2;21)(p13;q22.1)mat. Am J Med Genet 44(3):288–292CrossRef Kieran MW, Vekemans M, Robb LJ et al (1992) Portohepatic shunt in a Down syndrome patient with an interchange trisomy 47, XY,-2,+der(2), +der(21)t(2;21)(p13;q22.1)mat. Am J Med Genet 44(3):288–292CrossRef
12.
Zurück zum Zitat Ohno T, Muneuchi J, Ihara K et al (2008) Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Pediatrics 121(4):e892–e899CrossRef Ohno T, Muneuchi J, Ihara K et al (2008) Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Pediatrics 121(4):e892–e899CrossRef
13.
Zurück zum Zitat Massin M, Verloes A, Jamblin P (1999) Cardiac anomalies associated with congenital absence of the portal vein. Cardiol Young 9(5):522–525CrossRef Massin M, Verloes A, Jamblin P (1999) Cardiac anomalies associated with congenital absence of the portal vein. Cardiol Young 9(5):522–525CrossRef
14.
Zurück zum Zitat Kohda E, Saeki M, Nakano M et al (1999) Congenital absence of the portal vein in a boy. Pediatr Radiol 29(4):235–237CrossRef Kohda E, Saeki M, Nakano M et al (1999) Congenital absence of the portal vein in a boy. Pediatr Radiol 29(4):235–237CrossRef
15.
Zurück zum Zitat Eroglu Y, Donaldson J, Sorensen LG et al (2004) Improved neurocognitive function after radiologic closure of congenital portosystemic shunts. J Pediatr Gastroenterol Nutr 39(4):410–417CrossRef Eroglu Y, Donaldson J, Sorensen LG et al (2004) Improved neurocognitive function after radiologic closure of congenital portosystemic shunts. J Pediatr Gastroenterol Nutr 39(4):410–417CrossRef
16.
Zurück zum Zitat Hoover W, Ackerman V, Schamberger M et al (2008) The congenital porto-caval fistula: a unique presentation and novel intervention. Pediatr Pulmonol 43(2):196–199CrossRef Hoover W, Ackerman V, Schamberger M et al (2008) The congenital porto-caval fistula: a unique presentation and novel intervention. Pediatr Pulmonol 43(2):196–199CrossRef
17.
Zurück zum Zitat Hofstaetter C, Plath H, Hansmann M (2000) Prenatal diagnosis of abnormalities of the fetal venous system. Ultrasound Obstet Gynecol 15(3):231–241CrossRef Hofstaetter C, Plath H, Hansmann M (2000) Prenatal diagnosis of abnormalities of the fetal venous system. Ultrasound Obstet Gynecol 15(3):231–241CrossRef
18.
Zurück zum Zitat Achiron R, Hegesh J, Yagel S et al (2000) Abnormalities of the fetal central veins and umbilico-portal system: prenatal ultrasonographic diagnosis and proposed classification. Ultrasound Obstet Gynecol 16(6):539–548CrossRef Achiron R, Hegesh J, Yagel S et al (2000) Abnormalities of the fetal central veins and umbilico-portal system: prenatal ultrasonographic diagnosis and proposed classification. Ultrasound Obstet Gynecol 16(6):539–548CrossRef
19.
Zurück zum Zitat Uchino T, Matsuda I, Endo F (1999) The long-term prognosis of congenital portosystemic venous shunt. J Pediatr 135(2):254–256CrossRef Uchino T, Matsuda I, Endo F (1999) The long-term prognosis of congenital portosystemic venous shunt. J Pediatr 135(2):254–256CrossRef
20.
Zurück zum Zitat Franchi-Abella S, Branchereau S, Lambert V et al (2010) Complications of congenital portosystemic shunts in children: therapeutic options and outcomes. J Pediatr Gastroenterol Nutr 51(3):322–330PubMed Franchi-Abella S, Branchereau S, Lambert V et al (2010) Complications of congenital portosystemic shunts in children: therapeutic options and outcomes. J Pediatr Gastroenterol Nutr 51(3):322–330PubMed
21.
Zurück zum Zitat Gallego C, Miralles M, Marin C et al (2004) Congenital hepatic shunts. Radiographics 24(3):755–772CrossRef Gallego C, Miralles M, Marin C et al (2004) Congenital hepatic shunts. Radiographics 24(3):755–772CrossRef
22.
Zurück zum Zitat Hara Y, Sato Y, Yamamoto S et al (2013) Successful laparoscopic division of a patent ductus venosus: report of a case. Surg Today 43(4):434–438CrossRef Hara Y, Sato Y, Yamamoto S et al (2013) Successful laparoscopic division of a patent ductus venosus: report of a case. Surg Today 43(4):434–438CrossRef
Metadaten
Titel
Laparoscopic ligation of portosystemic shunt for the treatment of congenital intrahepatic portosystemic shunt in one newborn infant
verfasst von
Jin-Shan Zhang
Long Li
Publikationsdatum
06.10.2020
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Surgery International / Ausgabe 12/2020
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-020-04753-6

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