{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,8]],"date-time":"2026-03-08T22:45:01Z","timestamp":1773009901731,"version":"3.50.1"},"reference-count":5,"publisher":"Oxford University Press (OUP)","issue":"6","license":[{"start":{"date-parts":[[2022,6,16]],"date-time":"2022-06-16T00:00:00Z","timestamp":1655337600000},"content-version":"vor","delay-in-days":15,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,6,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Mayer\u2013Rokitansky\u2013K\u00fcster\u2013Hauser (MRKH) syndrome is the second most common cause of primary amenorrhea with an incidence of 1:4000\u20135000 women. It is characterized by aplasia or hypoplasia of the uterus and the upper two-thirds of the vagina with normal ovaries and tubes and a normal secondary sexual characteristics. The occurrence of leiomyoma is common but it is rare to have leiomyoma in uterine remnant in MRKH syndrome. Although few cases of MRKH syndrome with leiomyoma have been reported in the literature, none presented with urinary retention. Here, we report a case of 28-year-old women who presented with urinary retention that unmasked deeply embedded huge fibroids in pelvis arising from a rudimentary uterine horns and its safe management via laparoscopic approach.<\/jats:p>","DOI":"10.1093\/jscr\/rjac291","type":"journal-article","created":{"date-parts":[[2022,6,16]],"date-time":"2022-06-16T15:03:41Z","timestamp":1655391821000},"source":"Crossref","is-referenced-by-count":4,"title":["Urinary retention unveiling deeply embedded multiple leiomyomas in women with Mayer\u2013Rokitansky\u2013Kuster\u2013Hauser syndrome and its successful laparoscopic management: a case-report and literature review"],"prefix":"10.1093","volume":"2022","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9742-4330","authenticated-orcid":false,"given":"Namita","family":"Jain","sequence":"first","affiliation":[{"name":"Obstetrics and Gynecology Department, Paras Hospital , Gurugram 122002 , India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Isha","family":"Kriplani","sequence":"additional","affiliation":[{"name":"Obstetrics and Gynecology Department, Paras Hospital , Gurugram 122002 , India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Seema","family":"Sharma","sequence":"additional","affiliation":[{"name":"Obstetrics and Gynecology Department, Paras Hospital , Gurugram 122002 , India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shaily","family":"Hanumantaiya","sequence":"additional","affiliation":[{"name":"Obstetrics and Gynecology Department, Paras Hospital , Gurugram 122002 , India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alka","family":"Kriplani","sequence":"additional","affiliation":[{"name":"Obstetrics and Gynecology Department, Paras Hospital , Gurugram 122002 , India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2022,6,16]]},"reference":[{"key":"2022061615030697700_ref1","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1186\/1477-7827-10-57","article-title":"Malformations in a cohort of 284 women with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH)","volume":"10","author":"Oppelt","year":"2012","journal-title":"Reprod Biol Endocrinol"},{"key":"2022061615030697700_ref2","doi-asserted-by":"crossref","first-page":"5895","DOI":"10.3390\/ijerph18115895","article-title":"The rare, unexpected condition of a twisted leiomyoma in Mayer-Rokitansky-K\u00fcster-Hauser (MRKH) syndrome: etiopathogenesis, diagnosis and management. Our experience and narrative review of the literature","volume":"18","author":"Romano","year":"2021","journal-title":"Int J Environ Res Public Health"},{"key":"2022061615030697700_ref3","first-page":"3725043","article-title":"Case report rare case of leiomyoma and adenomyosis in Mayer-RokitanskyKuster-Hauser syndrome","volume":"2016","author":"Hoo","year":"2016","journal-title":"Case Rep Obstet Gynecol"},{"key":"2022061615030697700_ref4","doi-asserted-by":"crossref","first-page":"4147","DOI":"10.18203\/2320-1770.ijrcog20174080","article-title":"Fibroid originated from rudimentary horn in mullerian agenesis","volume":"6","author":"Deepika","year":"2017","journal-title":"Int J Reprod Contracept Obstet Gynecol"},{"key":"2022061615030697700_ref5","doi-asserted-by":"crossref","first-page":"30","DOI":"10.5005\/jp-journals-10016-1037","article-title":"Large fibroid arising from Mullerian remnant mimicking as ovarian neoplasm in a woman with MRKH syndrome","volume":"3","author":"Singh","year":"2012","journal-title":"Int J Infertility Fetal Med"}],"container-title":["Journal of Surgical Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/academic.oup.com\/jscr\/article-pdf\/2022\/6\/rjac291\/44083061\/rjac291.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/academic.oup.com\/jscr\/article-pdf\/2022\/6\/rjac291\/44083061\/rjac291.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,6,16]],"date-time":"2022-06-16T15:03:46Z","timestamp":1655391826000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/jscr\/article\/doi\/10.1093\/jscr\/rjac291\/6608963"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,6,1]]},"references-count":5,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2022,6,1]]}},"URL":"https:\/\/doi.org\/10.1093\/jscr\/rjac291","relation":{},"ISSN":["2042-8812"],"issn-type":[{"value":"2042-8812","type":"electronic"}],"subject":[],"published-other":{"date-parts":[[2022,6]]},"published":{"date-parts":[[2022,6,1]]},"article-number":"rjac291"}}