孕期双子宫：一种罕见的苗勒管异常病例报告
Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report.
作者信息
Jorgensen Colin, Lusiak Monika
机构信息
AMITA Health Resurrection Medical Center, Department of Emergency Medicine, Chicago, Illinois.
出版信息
Clin Pract Cases Emerg Med. 2021 Nov;5(4):447-449. doi: 10.5811/cpcem.2021.7.53212.
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.
引言
双子宫，即“双子宫体”，是最罕见的苗勒管畸形（MDA）之一。由于其罕见性，关于这种先天性缺陷的总体结局的数据稀少，但它可能与多种并发症相关，包括妊娠相关和非妊娠相关的并发症。
病例报告
在本病例中，一名35岁的孕妇出现阴道出血，随后经阴道超声成像诊断为双子宫。
结论
尽管双子宫罕见，但临床医生应了解苗勒管畸形及其与妊娠相关的并发症。
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