» Articles » PMID: 30194461

Ultrasound with Doppler Evaluation of Congenital Hepatic Vascular Shunts

Overview
Journal Pediatr Radiol
Specialty Pediatrics
Date 2018 Sep 9
PMID 30194461
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Congenital aberrant hepatic vascular communications result from intrahepatic or extrahepatic errors in vascular development or involution during the transition from fetal to newborn hepatic circulation. These hepatic vascular shunts can be fortuitously discovered and asymptomatic, or can cause symptoms of varying severity, often presenting diagnostic dilemmas. Some hepatic vascular shunts resolve spontaneously while others require interventional radiologic or surgical closure. Affected patients are often first studied with real-time and Doppler ultrasound, so radiologists should familiarize themselves with the expected ultrasound findings of these vascular shunts for effective diagnosis, triage and management. In this review, the authors focus on ultrasound and Doppler findings of hepatic vascular shunts with underlying embryology, clinical features and management strategies. Broadly, these aberrant hepatic vascular communications include portosystemic venous shunts (which can be intra- or extrahepatic and include persistent patent ductus venosus), arterioportal, arteriovenous or mixed shunts.

Citing Articles

Congenital Extrahepatic Portosystemic Shunt Complicated by the Development of Hepatoblastoma: A Case Report and Review of Literature.

AlMheiri M, Mrayyan H, Krishnamurthy B, Dsouza A Cureus. 2024; 16(2):e54508.

PMID: 38516443 PMC: 10955446. DOI: 10.7759/cureus.54508.


Prenatal ultrasonographic features and follow-up outcomes of 19 cases of congenital intrahepatic portosystemic venous shunts diagnosed during the foetal period.

Zhu L, Wu H, Cong X, Li S, Li Q, Dong X Insights Imaging. 2022; 13(1):169.

PMID: 36264515 PMC: 9584029. DOI: 10.1186/s13244-022-01310-8.


Hepatic hemangiomas in childhood: the spectrum of radiologic findings. A pictorial essay.

Esposito F, DAuria D, Ferrara D, Esposito P, Gaglione G, Zeccolini M J Ultrasound. 2022; 26(1):261-276.

PMID: 36071345 PMC: 10063746. DOI: 10.1007/s40477-022-00714-y.


Prenatal diagnosis and management of a giant intrahepatic arteriovenous malformation-Sonographic findings, clinical implications, and treatment.

Walter A, Calite E, Muller A, Kalff J, Meyer C, Geipel A Clin Case Rep. 2022; 10(8):e6175.

PMID: 35937027 PMC: 9347331. DOI: 10.1002/ccr3.6175.


Symptomatic congenital hemangiomatosis in a neonate: Imaging of a life-threatening presentation with multifocal liver involvement.

Ramdani H, El Haddad S, Allali N, Chat L Radiol Case Rep. 2022; 17(9):3126-3131.

PMID: 35774051 PMC: 9237947. DOI: 10.1016/j.radcr.2022.05.071.


References
1.
Gorincour G, Droulle P, Guibaud L . Prenatal diagnosis of umbilicoportosystemic shunts: report of 11 cases and review of the literature. AJR Am J Roentgenol. 2004; 184(1):163-8. DOI: 10.2214/ajr.184.1.01840163. View

2.
Wu L, Zhao L, Lu Y, He L, Hu X . Interventional embolization of congenital intrahepatic shunts in children. Pediatr Radiol. 2015; 46(4):541-7. DOI: 10.1007/s00247-015-3497-3. View

3.
Billing J, Jamieson N . Hepatic arterioportal fistula: a curable cause of portal hypertension in infancy. HPB Surg. 1997; 10(5):311-4. PMC: 2423894. DOI: 10.1155/1997/58026. View

4.
Kwapisz L, Wells M, Aljudaibi B . Abernethy malformation: congenital absence of the portal vein. Can J Gastroenterol Hepatol. 2015; 28(11):587-8. PMC: 4277169. DOI: 10.1155/2014/675812. View

5.
Makin E, Davenport M . Fetal and neonatal liver tumours. Early Hum Dev. 2010; 86(10):637-42. DOI: 10.1016/j.earlhumdev.2010.08.023. View