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罗伯特子宫盲半腔妊娠:一例报告

Pregnancy in the blind hemi-cavity of Robert's uterus: a case report.

作者信息

Liu Yan, Wang Shanshan, Hong Yue, Wang Jia, Niu Junqiao, Li Xiaojuan, Li Hui, Wang Yan

机构信息

Department of Radiology, People's Hospital of Xinjiang Uygur Autonomous region, China.

出版信息

Radiol Case Rep. 2021 Feb 24;16(5):1085-1088. doi: 10.1016/j.radcr.2021.02.013. eCollection 2021 May.

Abstract

Robert's uterus is a rare Müllerian malformation first characterized by a French gynecologist Héléne Robert in 1969. It represents an asymmetric division of the uterine cavity. A 45-year-old female patient presented with vaginal bleeding and vague abdominal pain for the course of 20 days, with a blood human chorionic gonadotropin level of 10331.00 mIU/mL, and a gestational sac in the right uterine horn without a fetal heart beat revealed by the ultrasound. Ectopic pregnancy in the right uterine horn seemed to be the most likely diagnosis. Laparoscopic and hysteroscopic attempts to terminate the pregnancy failed. A pelvic magnetic resonance imaging (MRI) performed after the surgery demonstrated Robert's uterus with pregnancy in the blind hemicavity. When a pregnancy sac has been revealed by an ultrasound but nothing has been found by a hysteroscopy, a possibility of uterine malformation should be considered. Radiologists and gynecologists should consider the application of MRI for diagnosis of congenital Müllerian uterine anomalies.

摘要

罗伯特子宫是一种罕见的苗勒管畸形,1969年由法国妇科医生海伦·罗伯特首次描述。它表现为子宫腔的不对称分隔。一名45岁女性患者出现阴道出血和模糊腹痛20天,血人绒毛膜促性腺激素水平为10331.00 mIU/mL,超声显示右子宫角有妊娠囊但无胎心搏动。右子宫角异位妊娠似乎是最可能的诊断。腹腔镜和宫腔镜终止妊娠的尝试均失败。术后盆腔磁共振成像(MRI)显示为罗伯特子宫,妊娠位于盲半腔。当超声显示有妊娠囊但宫腔镜检查未发现任何异常时,应考虑子宫畸形的可能性。放射科医生和妇科医生应考虑应用MRI诊断先天性苗勒管子宫异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c955/7921196/cebf9f1b2d88/gr1.jpg

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