Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/6782
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dc.contributor.authorYammine, Kabalaneen_US
dc.contributor.authorOsman, Danien_US
dc.contributor.authorDaher, Jihaden_US
dc.contributor.authorSalha, Makramen_US
dc.contributor.authorMouawad, Sabineen_US
dc.date.accessioned2023-04-18T08:01:46Z-
dc.date.available2023-04-18T08:01:46Z-
dc.date.issued2023-06-01-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/6782-
dc.description.abstractAcquired uterine arteriovenous malformation is a rare condition, sometimes provoking abnormal life-threatening uterine hemorrhage. Here, we present the case of a 30-year-old healthy woman who developed heavy vaginal bleeding after dilatation and suctioning of the placenta 1 month after the delivery of a nonviable fetus. An ultrasound was performed which showed the appearance of a large exacerbation of a vessel with positive fetal sounds, normal cardiac movement, and normal morphological analysis. The patient was successfully treated with unilateral superselective embolization, distal to the ovarian supply, maintaining normal supply to the uterus and ovaries restoring normal menstruation, and showed complete resolution of the arteriovenous malformation.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.subjectHemorrhageen_US
dc.subjectUterine arteriovenous malformationen_US
dc.subjectUterine artery embolizationen_US
dc.titleAcquired uterine arteriovenous malformation treated with superselective embolization: Case reporten_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.radcr.2023.03.018-
dc.identifier.scopus2-s2.0-85152144335-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85152144335-
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume18en_US
dc.description.issue6en_US
dc.description.startpage2204en_US
dc.description.endpage2208en_US
dc.date.catalogued2023-04-18-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.radcr.2023.03.018en_US
dc.relation.ispartoftextRadiology Case Reportsen_US
Appears in Collections:Faculty of Medicine
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