Behrens Michaela, Licata Michael, Lee Ji-Young
Department of Obstetrics and Gynecology, Sisters of Charity Hospital, University at Buffalo, Buffalo, New York, 14214, USA.
Department of Radiology, Sisters of Charity Hospital, University at Buffalo, Buffalo, New York, 14214, USA.
Int J Surg Case Rep. 2020;68:4-7. doi: 10.1016/j.ijscr.2020.01.052. Epub 2020 Feb 11.
The rudimentary noncommunicating horn with a functional endometrial cavity is rare and often challenging to diagnose because of the variety in clinical features. We present a case of a patient for whom the diagnosis of a uterine horn was missed during the prior cesarean section, which later successfully treated with robotic-assisted laparoscopic removal of a rudimentary noncommunicating horn of uterus and ipsilateral tube.
A 20-year old woman, gravida 3 para 2, presented with a complaint of acute and severe pelvic pain with fever. Multiple imaging modalities of pelvis and abdomen showed an 8 cm right-sided pelvic mass with a tubular structure adjacent to the uterus. The pelvic inflammatory disease was diagnosed and treated with intravenous antibiotics. After reviewing multiple radiology images, Müllerian anomaly was suspected, and the rudimentary horn with the fallopian tube was confirmed via diagnostic hysteroscopy and laparoscopy. Subsequently, robotic-assisted laparoscopic removal of the right horn with the fallopian tube was performed.
Assessment of a rudimentary noncommunicating horn with unicornuate uterus can be achieved by several radiology methods, including computed tomography, magnetic resonance imaging, two and 3-dimensional ultrasonography, hysterosalpingogram, and sonohysterography. In addition, evaluation of concomitant skeletal and renal anomalies is essential in enhancing diagnostic accuracy. In our case, the Müllerian anomaly with delayed onset complications was diagnosed by multiple imaging studies and treated successfully.
The early and correct diagnosis of the Müllerian anomaly remains difficult but essential as misdiagnosis can be associated with serious complications in patients.
具有功能性子宫内膜腔的始基非交通性子宫角极为罕见,因其临床特征多样,诊断往往具有挑战性。我们报告一例患者,其在先前剖宫产时漏诊了子宫角,后来通过机器人辅助腹腔镜手术成功切除了始基非交通性子宫角及同侧输卵管。
一名20岁女性,孕3产2,因急性剧烈盆腔疼痛伴发热就诊。骨盆和腹部的多种影像学检查显示右侧盆腔有一个8厘米的肿块,与子宫相邻有管状结构。诊断为盆腔炎并给予静脉抗生素治疗。在复查多张放射影像后,怀疑为苗勒管畸形,通过诊断性宫腔镜检查和腹腔镜检查确诊为带有输卵管的始基子宫角。随后,进行了机器人辅助腹腔镜下右侧子宫角及输卵管切除术。
对于单角子宫合并始基非交通性子宫角的评估可通过多种放射学方法实现,包括计算机断层扫描、磁共振成像、二维和三维超声检查、子宫输卵管造影和宫腔超声造影。此外,评估合并的骨骼和肾脏异常对于提高诊断准确性至关重要。在我们的病例中,通过多项影像学研究诊断出伴有延迟发作并发症的苗勒管畸形,并成功进行了治疗。
苗勒管畸形的早期正确诊断仍然困难但至关重要,因为误诊可能会给患者带来严重并发症。