{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,8]],"date-time":"2026-04-08T13:50:09Z","timestamp":1775656209154,"version":"3.50.1"},"reference-count":15,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"C","license":[{"start":{"date-parts":[[2024,2,1]],"date-time":"2024-02-01T00:00:00Z","timestamp":1706745600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,2,1]],"date-time":"2024-02-01T00:00:00Z","timestamp":1706745600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,1,18]],"date-time":"2024-01-18T00:00:00Z","timestamp":1705536000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2024,2]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Introduction:<\/jats:title>\n                    <jats:p>The management of Budd-Chiari syndrome is determined on the basis of the severity of the disease. There are no standard guidelines regarding the management of Budd-Chiari syndrome in children, particularly in cases of liver transplantation. Therefore, we present a case of a pediatric patient with Budd-Chiari syndrome treated with liver transplantation.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Case presentation:<\/jats:title>\n                    <jats:p>A female patient aged 1 year and 8 months presented to the hospital with an enlarged stomach in the last 1.5 months before admission. The patient was moderately ill, malnourished, and jaundiced. Liver biopsy revealed fibrosis in the portal area and confluent necrosis caused by vascular disorders. Magnetic resonance imaging (MRI) revealed a nutmeg liver and ascites due to the stenosis of the inferior vena cava at the level of the liver and the middle and left hepatic veins. The patient underwent living-donor liver transplantation. The occlusion of the proximal right hepatic vein due to the presence of a membrane was identified as the cause of Budd-Chiari syndrome in this case. Postoperatively, the patient's condition was stable and there was no sepsis or any other complications.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Clinical discussion:<\/jats:title>\n                    <jats:p>Prothrombotic factors are often the underlying cause of more than 80 % of Budd-Chiari syndrome cases. Protein C deficiency is suspected to be a prothrombotic factor that triggers Budd-Chiari syndrome in patients. Liver transplantation is the treatment of choice for patients with Budd-Chiari syndrome who were not treated with anticoagulation therapy, angioplasty, and TIPS.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>Living-donor liver transplantation has a good outcome in the management of pediatric patients with Budd-Chiari syndrome.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Highlights<\/jats:title>\n                  <\/jats:sec>","DOI":"10.1016\/j.ijscr.2024.109294","type":"journal-article","created":{"date-parts":[[2024,1,20]],"date-time":"2024-01-20T04:26:55Z","timestamp":1705724815000},"update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":1,"title":["Living donor liver transplantation on pediatric patient with Budd-Chiari syndrome: Case report and literature review"],"prefix":"10.1097","volume":"115","author":[{"given":"Tri Hening","family":"Rahayatri","sequence":"first","affiliation":[{"name":"Faculty of Medicine, Universitas Indonesia, Department of Pediatric Surgery, Cipto Mangunkusumo Hospital, Jakarta, Indonesia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jason","family":"Ruslie","sequence":"additional","affiliation":[{"name":"Faculty of Medicine, Universitas Indonesia, Department of Surgery, Cipto Mangunkusumo Hospital, Jakarta, Indonesia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mureo","family":"Kasahara","sequence":"additional","affiliation":[{"name":"Department of Transplantation, National Center for Child Health and Development, Tokyo, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-90-20260408","first-page":"1","article-title":"Budd-Chiari Syndrome","author":"X Q.","year":"2019","journal-title":"Treasure Island (FL)."},{"issue":"6","key":"R2-90-20260408","doi-asserted-by":"crossref","first-page":"578","DOI":"10.1056\/NEJMra020282","article-title":"The Budd-Chiari syndrome","volume":"350","author":"Menon,","year":"2004","journal-title":"N. Engl. J. Med."},{"issue":"4","key":"R3-90-20260408","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1016\/j.clinre.2018.10.014","article-title":"Epidemiology of Budd-Chiari syndrome: a systematic review and meta-analysis","volume":"43","author":"Li,","year":"2019","journal-title":"Clin. Res. Hepatol. Gastroenterol."},{"issue":"3","key":"R4-90-20260408","doi-asserted-by":"crossref","first-page":"167","DOI":"10.7326\/0003-4819-151-3-200908040-00004","article-title":"Etiology, management, and outcome of the Budd-Chiari syndrome","volume":"151","author":"Darwish Murad,","year":"2009","journal-title":"Ann. Intern. Med."},{"issue":"5","key":"R5-90-20260408","doi-asserted-by":"crossref","first-page":"1337","DOI":"10.1002\/hep.1840210518","article-title":"Which is the best surgery for Budd-Chiari syndrome: venous decompression or liver transplantation? A single-center experience with 50 patients","volume":"21","author":"Ringe,","year":"1995","journal-title":"Hepatology"},{"issue":"2","key":"R6-90-20260408","doi-asserted-by":"crossref","first-page":"144","DOI":"10.1002\/lt.21282","article-title":"Eighteen years of liver transplantation experience in patients with advanced Budd-Chiari syndrome","volume":"14","author":"Ulrich,","year":"2008","journal-title":"Liver Transpl."},{"issue":"5","key":"R7-90-20260408","doi-asserted-by":"crossref","first-page":"1136","DOI":"10.1097\/JS9.0000000000000373","article-title":"The SCARE 2023 guideline: updating consensus surgical CAse REport (SCARE) guidelines","volume":"109","author":"Sohrabi,","year":"2023","journal-title":"Int. J. 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Hepatol."},{"issue":"1","key":"R10-90-20260408","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1186\/s40792-021-01224-5","article-title":"Living donor liver transplantation for Budd-Chiari syndrome with right posterior segment graft and patch plasty using the superficial femoral vein: a case report.","volume":"7","author":"Une","year":"2021","journal-title":"Surg Case Rep."},{"issue":"10","key":"R11-90-20260408","first-page":"1783","article-title":"The budd-Chiari syndrome in a child: a case report and review of the literature","volume":"6","author":"Misra,","year":"2012","journal-title":"J. Clin. Diagn. Res."},{"issue":"2","key":"R12-90-20260408","doi-asserted-by":"crossref","first-page":"e17","DOI":"10.1016\/j.clinre.2019.10.008","article-title":"Obstructed membranous transformation of the inferior vena cava in patients with hepatic vein-type Budd-Chiari syndrome: a case series","volume":"44","author":"Ding,","year":"2020","journal-title":"Clin. Res. Hepatol. 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