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dc.contributor.authorWali Jebran, Farzana
dc.contributor.authorJebran, Ahmad M.
dc.contributor.authorJalalzai, Rana
dc.contributor.authorSaadaat, Ramin
dc.contributor.authorAlizai, Huma
dc.contributor.authorSadat, Karima
dc.date.accessioned2025-06-30T16:53:45Z
dc.date.available2025-06-30T16:53:45Z
dc.date.issued2025-03-10
dc.identifier.urihttps://hdl.handle.net/1721.1/159840
dc.description.abstractCongenital uterine anomalies with outflow tract obstruction caused by abnormal Mullerian duct system development are rare conditions that can lead to painful pelvic emergencies such as hematometra. A unicornuate uterus with a rudimentary horn occurs in about 2.4–13% of all Müllerian duct anomalies with a prevalence of 1 in 100000 fertile women. Clinical symptoms such as dysmenorrhea, dyspareunia, and acute and chronic pelvic pain usually develop at and after menarche. Accurate diagnosis and timely surgical intervention are crucial to prevent complications such as adenomyosis, endometriosis, and infertility. A 21-year-old nulligravida Afghan female presented with severe chronic pelvic pain that worsened during menstruation and coitus. Ultrasonography and magnetic resonance imaging (MRI) revealed two separate uterine bodies. The left body was a unicornuate uterus with an endometrial lining connected to the cervix and the vaginal canal. The right body showed a functioning non-communicating rudimentary horn containing hematometra without a cervical opening. The patient underwent a hemi-hysterectomy and the rudimentary horn was removed. The histopathological findings revealed adenomyosis with cystic changes. The patient recovered after the operation and her severe pain subsided. This case underscores the importance of timely diagnosis and management of rare non-communicating functioning rudimentary horn anomalies that occur in less than 0.06% of reproductive-age women. Notably, this report adds to the limited literature on this anomaly where the rudimentary horn contained extensive adenomyosis, highlighting the potential for significant histopathological changes in such anomalies. Precise diagnosis and surgical excision are critical to prevent complications.en_US
dc.publisherSpringer International Publishingen_US
dc.relation.isversionofhttps://doi.org/10.1007/s42399-025-01798-3en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer International Publishingen_US
dc.titleAdenomyosis and Hematometra in a Non-communicating Rudimentary Horn of a Unicornuate Uterus: A Case Reporten_US
dc.typeArticleen_US
dc.identifier.citationWali Jebran, F., Jebran, A.M., Jalalzai, R. et al. Adenomyosis and Hematometra in a Non-communicating Rudimentary Horn of a Unicornuate Uterus: A Case Report. SN Compr. Clin. Med. 7, 57 (2025).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.relation.journalSN Comprehensive Clinical Medicineen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2025-03-27T13:50:32Z
dc.language.rfc3066en
dc.rights.holderThe Author(s), under exclusive licence to Springer Nature Switzerland AG
dspace.embargo.termsY
dspace.date.submission2025-03-27T13:50:32Z
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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