{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,21]],"date-time":"2026-02-21T10:51:15Z","timestamp":1771671075249,"version":"3.50.1"},"reference-count":9,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2022,4,26]],"date-time":"2022-04-26T00:00:00Z","timestamp":1650931200000},"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. Cardiovasc. Med."],"abstract":"<jats:p>Intravenous leiomyomatosis (IVL) is a distinct uterine leiomyoma, even rare when combined with intracardiac invasion. Although leiomyomas are histologically benign, intracardiac metastasis may cause circulatory failure and death. Herein, we report a 55-year-old woman with a tricuspid chordae mass on echocardiography. Subsequently, gynecological ultrasonography revealed that the patient had masses in the ovaries, internal iliac vein, and inferior vena cava. The patient successfully underwent resection of the tricuspid chordae tendinea mass and implantation of the tricuspid annuloplasty ring. The patient underwent inferior vena cava, common iliac vein, hysterectomy, and bilateral adnexectomy after 4 months. To our knowledge, the present study is the first reported case with such a rare combination.<\/jats:p>","DOI":"10.3389\/fcvm.2022.871983","type":"journal-article","created":{"date-parts":[[2022,4,26]],"date-time":"2022-04-26T06:36:20Z","timestamp":1650954980000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["A Rare Case of Cardiac Metastatic Uterine Intravenous Leiomyomatosis"],"prefix":"10.3389","volume":"9","author":[{"given":"Xun","family":"Wu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Feng","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chukwuemeka Daniel","family":"Iroegbu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chengming","family":"Fan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"GuoBao","family":"Song","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2022,4,26]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"1240","DOI":"10.1016\/j.humpath.2010.10.015","article-title":"Intravenous leiomyomatosis of the uterus: a clinicopathologic study of 18 cases, with emphasis on early diagnosis and appropriate treatment strategies.","volume":"42","author":"Du","year":"2011","journal-title":"Hum Pathol."},{"key":"B2","doi-asserted-by":"publisher","first-page":"503.e501","DOI":"10.1016\/j.crad.2017.12.016","article-title":"Contrast-enhanced CT findings of intravenous leiomyomatosis.","volume":"73","author":"Wang","year":"2018","journal-title":"Clin Radiol."},{"key":"B3","doi-asserted-by":"publisher","first-page":"25","DOI":"10.5306\/wjco.v4.i1.25","article-title":"Uterine intravenous leiomyomatosis with cardiac extension: imaging characteristics and literature review.","volume":"4","author":"Xu","year":"2013","journal-title":"World J Clin Oncol."},{"key":"B4","doi-asserted-by":"publisher","first-page":"202","DOI":"10.1080\/00313020410001672075","article-title":"Death due to intravenous leiomyomatosis extending to the right pulmonary artery.","volume":"36","author":"Burke","year":"2004","journal-title":"Pathology."},{"key":"B5","first-page":"261","article-title":"Primary cardiac tumors.","volume":"38","author":"Leja","year":"2011","journal-title":"Tex Heart Inst J."},{"key":"B6","doi-asserted-by":"publisher","first-page":"434.e437","DOI":"10.1016\/j.echo.2008.12.025","article-title":"Multisided cardiac hemangiomas mimicking biatrial thrombus: atypically located cardiac hemangiomas of left atrial appendage and right atrium.","volume":"22","author":"Acikel","year":"2009","journal-title":"J Am Soc Echocardiogr."},{"key":"B7","doi-asserted-by":"publisher","first-page":"530","DOI":"10.1055\/s-0032-1322545","article-title":"A 30-year-single-center experience in atrial myxomas: from presentation to treatment and prognosis.","volume":"61","author":"Obrenovi\u0107-Kir\u0107anski","year":"2013","journal-title":"Thorac Cardiovasc Surg."},{"key":"B8","doi-asserted-by":"publisher","first-page":"1058","DOI":"10.1111\/jog.13012","article-title":"Vanishing intravenous leiomyomatosis after hysterectomy: assessment of the need to perform complete resection.","volume":"42","author":"Maneyama","year":"2016","journal-title":"J Obstet Gynaecol Res."},{"key":"B9","doi-asserted-by":"publisher","first-page":"324","DOI":"10.1016\/j.athoracsur.2013.05.097","article-title":"Primary leiomyoma: a rare space occupying lesion in the right ventricle.","volume":"97","author":"Song","year":"2014","journal-title":"Ann Thorac Surg."}],"container-title":["Frontiers in Cardiovascular Medicine"],"original-title":[],"link":[{"URL":"https:\/\/www.frontiersin.org\/articles\/10.3389\/fcvm.2022.871983\/full","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,4,26]],"date-time":"2022-04-26T06:36:22Z","timestamp":1650954982000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.frontiersin.org\/articles\/10.3389\/fcvm.2022.871983\/full"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,4,26]]},"references-count":9,"alternative-id":["10.3389\/fcvm.2022.871983"],"URL":"https:\/\/doi.org\/10.3389\/fcvm.2022.871983","relation":{},"ISSN":["2297-055X"],"issn-type":[{"value":"2297-055X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,4,26]]},"article-number":"871983"}}