{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T16:34:54Z","timestamp":1753893294485,"version":"3.41.2"},"reference-count":16,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2022,8,9]],"date-time":"2022-08-09T00:00:00Z","timestamp":1660003200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Surg."],"abstract":"<jats:p>Hereditary haemorrhagic telangiectasia (HHT) is a rare disease that lacks effective treatment. Here, the authors report the case of a 30-year-old woman presenting with abdominal pain accompanied by severe malnutrition. After a definite diagnosis of HHT involvement in the liver, liver transplantation was the first-choice treatment according to the guidelines of HHT. However, the patient firmly refused liver transplantation. Finally, a new type of surgery, right hemihepatectomy combined with ligation of the common hepatic artery and gastroduodenal artery, was performed based on careful study of the case and with the maximum benefit of the patient in mind. Although the patient developed transient liver dysfunction after surgery, she eventually recovered well and continued to be followed up. As far as we know, this is the first report of this kind of surgery for the treatment of intrahepatic HHT.<\/jats:p>","DOI":"10.3389\/fsurg.2022.900297","type":"journal-article","created":{"date-parts":[[2022,8,9]],"date-time":"2022-08-09T05:58:41Z","timestamp":1660024721000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["Right hemihepatectomy combined with ligation of the common hepatic artery and gastroduodenal artery for the treatment of intrahepatic HHT: A\u00a0case report"],"prefix":"10.3389","volume":"9","author":[{"given":"Jifeng","family":"Xiang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wei","family":"Xie","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cuncheng","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huaizhi","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2022,8,9]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"6395629","DOI":"10.1155\/2020\/6395629","article-title":"Hereditary Hemorrhagic Telangiectasia in a Sudanese Patient","volume":"2020","author":"Elawad","year":"2020","journal-title":"Case Rep Med"},{"key":"B2","doi-asserted-by":"publisher","first-page":"33","DOI":"10.1038\/gim.2013.66","article-title":"The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia","volume":"16","author":"Grosse","year":"2014","journal-title":"Genet Med"},{"key":"B3","doi-asserted-by":"publisher","first-page":"171","DOI":"10.1148\/rg.281075037","article-title":"Abdominal findings in hereditary hemorrhagic telangiectasia: pictorial essay on 2D and 3D findings with isotropic multiphase CT","volume":"28","author":"Siddiki","year":"2008","journal-title":"Radiographics"},{"key":"B4","doi-asserted-by":"publisher","first-page":"66","DOI":"10.1002\/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P","article-title":"Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)","volume":"91","author":"Shovlin","year":"2000","journal-title":"Am J Med Genet"},{"key":"B5","doi-asserted-by":"publisher","first-page":"989","DOI":"10.7326\/M20-1443","article-title":"Second international guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia","volume":"173","author":"Faughnan","year":"2020","journal-title":"Ann Intern Med"},{"key":"B6","doi-asserted-by":"publisher","first-page":"872","DOI":"10.1007\/s11605-007-0411-9","article-title":"Treatment of high output cardiac failure by flow-adapted hepatic artery banding (FHAB) in patients with hereditary hemorrhagic telangiectasia","volume":"12","author":"Koscielny","year":"2008","journal-title":"J Gastrointest Surg"},{"key":"B7","doi-asserted-by":"publisher","first-page":"281","DOI":"10.1177\/000313481107700314","article-title":"Individualized management of hepatic diseases in hereditary hemorrhagic telangiectasia","volume":"77","author":"Song","year":"2011","journal-title":"Am Surg"},{"key":"B8","doi-asserted-by":"publisher","first-page":"e238385","DOI":"10.1136\/bcr-2020-238385","article-title":"Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations","volume":"14","author":"Dunphy","year":"2021","journal-title":"BMJ Case Rep"},{"key":"B9","doi-asserted-by":"publisher","first-page":"12","DOI":"10.1186\/s13023-020-01579-2","article-title":"Predictors of mortality in patients with hereditary hemorrhagic telangiectasia","volume":"16","author":"Thompson","year":"2021","journal-title":"Orphanet J Rare Dis"},{"key":"B10","doi-asserted-by":"publisher","first-page":"3750","DOI":"10.3390\/jcm9113750","article-title":"The role of liver imaging in hereditary hemorrhagic telangiectasia","volume":"9","author":"Harwin","year":"2020","journal-title":"J Clin Med"},{"key":"B11","doi-asserted-by":"publisher","first-page":"179","DOI":"10.1016\/j.jhep.2015.07.040","article-title":"Vascular diseases of the liver","volume":"64","year":"2016","journal-title":"J Hepatol"},{"key":"B12","doi-asserted-by":"publisher","first-page":"323","DOI":"10.1007\/s001470050152","article-title":"Effective therapy for hepatic M. 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