{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T12:06:49Z","timestamp":1753877209948,"version":"3.41.2"},"reference-count":10,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2020,3,1]],"date-time":"2020-03-01T00:00:00Z","timestamp":1583020800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,3,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>We report a case of a 47-year-old female, with strong preoperative clinical and radiological suspicious of uterine leiomyosarcoma who underwent a total abdominal hysterectomy. Despite the final histology concluded as benign uterine leiomyoma, the loss of fumarate hydratase expression of the same specimen still put her at risk of having hereditary leiomyomatosis and renal cell carcinoma syndrome. Intraoperatively, an obstetric vacuum cup was used for uterine manipulation to avoid breaching of the uterine serosa.<\/jats:p>","DOI":"10.1093\/jscr\/rjaa044","type":"journal-article","created":{"date-parts":[[2020,2,17]],"date-time":"2020-02-17T12:11:37Z","timestamp":1581941497000},"source":"Crossref","is-referenced-by-count":1,"title":["Fumarase-deficient uterine leiomyoma: a case of a rare entity and surgical innovation"],"prefix":"10.1093","volume":"2020","author":[{"given":"Hong","family":"Lee","sequence":"first","affiliation":[{"name":"Department of Obstetrics and Gynaecology, Joondalup Health Campus, Joondalup, WA, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Saman","family":"Shafiezadeh","sequence":"first","affiliation":[{"name":"Department of Obstetrics and Gynaecology, Joondalup Health Campus, Joondalup, WA, 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