Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report
Introduction: Didelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Due to its rarity, data are sparse on overall outcomes associated with this congenital defect, but it may be associated with several complications, both pregnancy and non-pregnancy related. Case...
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eScholarship Publishing, University of California
2021
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oai:doaj.org-article:f3bfe48563054f33af90ad26d3660c9f2021-11-23T20:02:52ZDidelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report2474-252X10.5811/cpcem.2021.7.53212https://doaj.org/article/f3bfe48563054f33af90ad26d3660c9f2021-11-01T00:00:00Zhttps://escholarship.org/uc/item/6193p2vmhttps://doaj.org/toc/2474-252XIntroduction: Didelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Due to its rarity, data are sparse on overall outcomes associated with this congenital defect, but it may be associated with several complications, both pregnancy and non-pregnancy related. Case Report: In this case, a pregnant 35-year-old female with vaginal bleeding was subsequently diagnosed with uterus didelphys by transvaginal ultrasound imaging. Conclusion: Despite its rarity, clinicians should be aware of MDAs and their associated compli-cations with pregnancy.Colin JorgensenMonika LusiakeScholarship Publishing, University of CaliforniaarticleMedical emergencies. Critical care. Intensive care. First aidRC86-88.9ENClinical Practice and Cases in Emergency Medicine, Vol 5, Iss 4 (2021) |
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DOAJ |
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DOAJ |
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EN |
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Medical emergencies. Critical care. Intensive care. First aid RC86-88.9 |
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Medical emergencies. Critical care. Intensive care. First aid RC86-88.9 Colin Jorgensen Monika Lusiak Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report |
| description |
Introduction: Didelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Due to its rarity, data are sparse on overall outcomes associated with this congenital defect, but it may be associated with several complications, both pregnancy and non-pregnancy related. Case Report: In this case, a pregnant 35-year-old female with vaginal bleeding was subsequently diagnosed with uterus didelphys by transvaginal ultrasound imaging. Conclusion: Despite its rarity, clinicians should be aware of MDAs and their associated compli-cations with pregnancy. |
| format |
article |
| author |
Colin Jorgensen Monika Lusiak |
| author_facet |
Colin Jorgensen Monika Lusiak |
| author_sort |
Colin Jorgensen |
| title |
Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report |
| title_short |
Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report |
| title_full |
Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report |
| title_fullStr |
Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report |
| title_full_unstemmed |
Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report |
| title_sort |
didelphys uterus in pregnancy, an uncommon mullerian duct anomaly: a case report |
| publisher |
eScholarship Publishing, University of California |
| publishDate |
2021 |
| url |
https://doaj.org/article/f3bfe48563054f33af90ad26d3660c9f |
| work_keys_str_mv |
AT colinjorgensen didelphysuterusinpregnancyanuncommonmullerianductanomalyacasereport AT monikalusiak didelphysuterusinpregnancyanuncommonmullerianductanomalyacasereport |
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1718416129933705216 |