{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,14]],"date-time":"2025-05-14T11:47:44Z","timestamp":1747223264134,"version":"3.40.5"},"reference-count":10,"publisher":"Pensoft Publishers","issue":"5","license":[{"start":{"date-parts":[[2024,10,31]],"date-time":"2024-10-31T00:00:00Z","timestamp":1730332800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["FM"],"abstract":"<jats:p>The congenital extrahepatic portosystemic shunt is a rare anomaly characterized by aplasia or hypoplasia of intrahepatic portal venous branches that generate complete or partial extrahepatic shunting of portal venous intra-systemic veins. The clinical presentation is variable, including nausea, abdominal pain, anorexia, and jaundice. This entity has been associated with other congenital anomalies, and the most common are the cardiovascular anomalies. Imaging studies are essential to confirm the diagnosis, establish pre-operative planning, and determine the surgical procedure to be performed. We presented the case of a 15-year-old adolescent who had abdominal symptoms and was found to have a portal venous vascular abnormality.<\/jats:p>","DOI":"10.3897\/folmed.66.e124107","type":"journal-article","created":{"date-parts":[[2024,11,6]],"date-time":"2024-11-06T15:45:04Z","timestamp":1730907904000},"page":"726-730","source":"Crossref","is-referenced-by-count":0,"title":["Congenital extrahepatic portosystemic shunt in a teenager: a case report"],"prefix":"10.3897","volume":"66","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6615-1413","authenticated-orcid":true,"given":"Daniela","family":"Arias-Mari\u00f1o","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0005-5990-106X","authenticated-orcid":true,"given":"Alejandro","family":"Rojas-Urrea","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-5086-1121","authenticated-orcid":true,"given":"Duvan Felipe","family":"Velandia-Siabato","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0000-3570-9560","authenticated-orcid":true,"given":"Marlon Alberto","family":"Orozco-Mojica","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-3249-0933","authenticated-orcid":true,"given":"Andres Manuel","family":"Bohorquez-Diaz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9557-0900","authenticated-orcid":true,"given":"Lorena","family":"Garc\u00eda-Agudelo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2258","published-online":{"date-parts":[[2024,10,31]]},"reference":[{"key":"124107_B1","doi-asserted-by":"crossref","unstructured":"1. Kumar P, Bhatia M, Garg A, et al. Abernethy malformation: A comprehensive review. Diagn Interv Radiol 2022; 28(1):21\u20138.","DOI":"10.5152\/dir.2021.20474"},{"key":"124107_B2","doi-asserted-by":"crossref","unstructured":"2. Baiges A, Turon F, Sim\u00f3n-Talero M, et al. Congenital extrahepatic portosystemic shunts (Abernethy malformation): an international observational study. Hepatology 2020; 71(2):658\u201369.","DOI":"10.1002\/hep.30817"},{"key":"124107_B3","doi-asserted-by":"crossref","unstructured":"3. Azad S, Arya A, Sitaraman R, et al. Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature. Ann Pediatr Cardiol 2019; 12(3):240\u20137.","DOI":"10.4103\/apc.APC_185_18"},{"key":"124107_B4","doi-asserted-by":"crossref","unstructured":"4. Guo C, Zhong YM, Wang Q, et al. Diagnostic accuracy of multi-slice computed tomography in children with Abernethy malformation. BMC Med Imaging 2019; 19(1):97.","DOI":"10.1186\/s12880-019-0396-3"},{"key":"124107_B5","doi-asserted-by":"crossref","unstructured":"5. Pe\u010dek J, Fister P, Homan M. Abernethy syndrome in Slovenian children: Five case reports and review of literature. World J Gastroenterol 2020; 26(37):5731\u201344.","DOI":"10.3748\/wjg.v26.i37.5731"},{"key":"124107_B6","doi-asserted-by":"crossref","unstructured":"6. Lin Y, Li X, Li S, et al. Treatment option for abernethy malformation-two cases report and review of the literature. Front Pediatr 2020; 8:497447.","DOI":"10.3389\/fped.2020.497447"},{"key":"124107_B7","doi-asserted-by":"crossref","unstructured":"7. Castro Rodr\u00edguez J, Rodr\u00edguez Per\u00e1lvarez ML, Montero-\u00c1lvarez JL. Diagnosis and management of Abernethy syndrome. Rev Esp Enferm Dig 2024; 116(1):1\u20136.","DOI":"10.17235\/reed.2023.9781\/2023"},{"key":"124107_B8","doi-asserted-by":"crossref","unstructured":"8. El-Medany AY, Rego G, Williams M, et al. Multimodality imaging of Abernethy malformation. Echocardiography 2022; 39(3):524\u20137.","DOI":"10.1111\/echo.15324"},{"key":"124107_B9","doi-asserted-by":"crossref","unstructured":"9. Wu X, Gu W, Lin Y, et al. A rare presentation of type II Abernethy malformation and nephrotic syndrome: Case report and review. Open Life Sci 2022; 17(1):794\u20139.","DOI":"10.1515\/biol-2022-0086"},{"key":"124107_B10","doi-asserted-by":"crossref","unstructured":"10. DiPaola F, Trout AT, Walther AE, et al. Congenital portosystemic shunts in children: associations, complications, and outcomes. 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