{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,10,19]],"date-time":"2024-10-19T04:18:38Z","timestamp":1729311518246,"version":"3.27.0"},"reference-count":19,"publisher":"Japanese Society of Internal Medicine","issue":"20","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Intern. Med."],"published-print":{"date-parts":[[2024,10,15]]},"DOI":"10.2169\/internalmedicine.3270-23","type":"journal-article","created":{"date-parts":[[2024,2,25]],"date-time":"2024-02-25T22:12:03Z","timestamp":1708899123000},"page":"2787-2793","source":"Crossref","is-referenced-by-count":0,"title":["An Splenic Artery Aneurysm and Focal Nodular Hyperplasia Associated with an Abdominal Vascular Abnormality of Hereditary Hemorrhagic Telangiectasia"],"prefix":"10.2169","volume":"63","author":[{"given":"Satoru","family":"Hagiwara","sequence":"first","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Koichi","family":"Nakagawa","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Saiseikai Tondabayashi Hospital, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoriaki","family":"Komeda","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Naoshi","family":"Nishida","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akihiro","family":"Yoshida","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomoki","family":"Yamamoto","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takuya","family":"Matsubara","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masatoshi","family":"Kudo","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"962","reference":[{"key":"1","unstructured":"1. Osler W. On a family form of recurring epistaxis, associated with multiple telangiectasias of the skin and mucous membranes. Bull Johns Hopkins Hosp 12: 333-337, 1901."},{"key":"2","unstructured":"2. Hanes F. Multiple hereditary telangiectases causing hemorrhage (hereditary hemorrhage telangiectasia). Bull Johns Hopkins Hosp 20: 63-73, 1909."},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Begbie ME, Wallace GMF, Shovlin CL. Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): A view from the 21st century. Postgrad Med J 79: 18-24, 2003.","DOI":"10.1136\/pmj.79.927.18"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 91: 66-67, 2000.","DOI":"10.1002\/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Shovlin CL, Hughes JMB, Tuddenham EGD, et al. A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3. Nat Genet 6: 205-209, 1994.","DOI":"10.1038\/ng0294-205"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Johnson DW, Berg JN, Gallione CJ, et al. A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. Genome Res 5: 21-28, 1995.","DOI":"10.1101\/gr.5.1.21"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Ruiz-Llorente L, Gallardo-Vara E, Rossi E, Smadja DM, Botella LM, Bernabeu C. Endoglin and alk1 as therapeutic targets for hereditary hemorrhagic telangiectasia. Expert Opin Ther Targets 21: 933-947, 2017.","DOI":"10.1080\/14728222.2017.1365839"},{"key":"8","unstructured":"8. Reilly PJ, Nostrant TT. Clinical manifestations of hereditary hemorrhagic telangiectasia. Am J Gastroenterol 79: 363-367, 1984."},{"key":"9","doi-asserted-by":"publisher","unstructured":"9. Ianora AA, Memeo M, Sabba C, Cirulli A, Rotondo A, Angelelli G. Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement. Radiology 230: 250-259, 2004.","DOI":"10.1148\/radiol.2301021745"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Komiyama M, Ishiguro T, Yamada O, Morisaki H, Morisaki T. Hereditary hemorrhagic telangiectasia in Japanese patients. J Hum Genet 59: 37-41, 2014.","DOI":"10.1038\/jhg.2013.113"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Buscarini E, Danesino C, Plauchu H, et al. High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia. Ultrasound Med Biol 30: 1089-1097, 2004.","DOI":"10.1016\/j.ultrasmedbio.2004.08.004"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Sekiguchi N, Yamada D, Kobayashi S, et al. Partial hepatectomy for a patient with Rendu-Osler-Weber disease: a case report. Surg Case Rep 9: 7, 2023.","DOI":"10.1186\/s40792-023-01588-w"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Moulinet T, Mohamed S, Deibener-Kaminsky J, Jankowski R, Kaminsky P. High prevalence of arterial aneurysms in hereditary hemorrhagic telangiectasia. Int J Cardiol 176: 1414-1416, 2014.","DOI":"10.1016\/j.ijcard.2014.08.016"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Sellier J, Karam C, Beauchet A, et al. Higher prevalence of splenic artery aneurysms in hereditary hemorrhagic telangiectasia: vascular implications and risk factors. PLOS ONE 15: e0226681, 2020.","DOI":"10.1371\/journal.pone.0226681"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Chaer RA, Abularrage CJ, Coleman DM, et al. The Society for Vascular Surgery clinical practice guidelines on the management of visceral aneurysms. J Vasc Surg 72: 3S-39S, 2020.","DOI":"10.1016\/j.jvs.2020.01.039"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Pitton MB, Dappa E, Jungmann F, et al. Visceral artery aneurysms: incidence, management, and outcome analysis in a tertiary care center over one decade. Eur Radiol 25: 2004-2014, 2015.","DOI":"10.1007\/s00330-015-3599-1"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia (HHT). J Hepatol 46: 499-507, 2007.","DOI":"10.1016\/j.jhep.2006.12.008"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Hashimoto M, Tate E, Nishii T, Watari J, Shioya T, White RI. Angiography of hepatic vascular malformations associated with hereditary hemorrhagic telangiectasia. Cardiovasc Intervent Radiol 26: 177-180, 2003.","DOI":"10.1007\/s00270-002-1507-Y"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Morii K, Uematsu R, Yamamoto T, et al. Hepatocellular carcinoma in a patient with hereditary hemorrhagic telangiectasia. Intern Med 57: 3545-3549, 2018.","DOI":"10.2169\/internalmedicine.1056-18"}],"container-title":["Internal Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/63\/20\/63_3270-23\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,10,19]],"date-time":"2024-10-19T03:28:22Z","timestamp":1729308502000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/63\/20\/63_3270-23\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,10,15]]},"references-count":19,"journal-issue":{"issue":"20","published-print":{"date-parts":[[2024]]}},"URL":"https:\/\/doi.org\/10.2169\/internalmedicine.3270-23","relation":{},"ISSN":["0918-2918","1349-7235"],"issn-type":[{"type":"print","value":"0918-2918"},{"type":"electronic","value":"1349-7235"}],"subject":[],"published":{"date-parts":[[2024,10,15]]},"article-number":"3270-23"}}