Ladke Pooja, Ambhore Ashish N, Dhok Avinash, Mitra Kajal, Dalvi Vrushali
Department of Radiodiagnosis, NKP Salve Institute of Medical Sciences (NKPSIMS) and Lata Mangeshkar Hospital (LMH), Nagpur, IND.
Cureus. 2022 Dec 17;14(12):e32640. doi: 10.7759/cureus.32640. eCollection 2022 Dec.
Congenital uterine anomalies are a rare type of malformation involving female genitalia caused by abnormal development of the Mullerian duct system. Patients having an obstructive type of uterine anomalies are very much likely to develop obstetric and gynecological complications usually at the age of menarche or later in the course of life. In this case report, we present a case of a young female patient having severe dysmenorrhea which is caused by obstructive hematometra in the rudimentary horn which is not communicating with the uterine cavity. Ultrasonography (USG) was used to make a differential diagnosis of a probable congenital abnormality, which was subsequently validated by magnetic resonance imaging (MRI), which revealed a uterine cavity having a single cornu on the left side seen to be connecting with the cervix and a dilated rudimentary horn on the right side. The patient underwent the excision of the rudimentary horn laparoscopically. This case emphasizes the importance of identifying patients having anomalies involving the uterus to provide appropriate treatment to the patient and to prevent adverse outcomes for her reproductive potential.
先天性子宫异常是一种罕见的女性生殖器畸形类型,由苗勒管系统发育异常引起。患有梗阻型子宫异常的患者很可能在初潮年龄或之后的人生过程中出现妇产科并发症。在本病例报告中,我们呈现了一名年轻女性患者的病例,该患者因残角子宫积血导致严重痛经,且残角子宫与子宫腔不相通。超声检查(USG)用于对可能的先天性异常进行鉴别诊断,随后通过磁共振成像(MRI)得到证实,MRI显示子宫腔左侧有一个单角与宫颈相连,右侧有一个扩张的残角。患者接受了腹腔镜下残角子宫切除术。该病例强调了识别子宫异常患者以给予适当治疗并防止对其生殖潜能产生不良后果的重要性。