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首页> 外文期刊>International Journal of Surgery Case Reports >The infected hematometra in a rudimentary noncommunicating horn misdiagnosed as pelvic mass: A case report
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The infected hematometra in a rudimentary noncommunicating horn misdiagnosed as pelvic mass: A case report

机译:被感染的血管瘤中的血管瘤被误诊为骨盆质量:案例报告

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Introduction 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. Presentation of case 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. Discussion 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. Conclusion The early and correct diagnosis of the Müllerian anomaly remains difficult but essential as misdiagnosis can be associated with serious complications in patients.
机译:介绍基本的非交通喇叭与功能子宫腔是罕见的,往往具有挑战性,因为在临床特征的各种诊断。我们提出了一个人子宫角的诊断现有剖宫产,后来成功地与机器人辅助腹腔镜切除子宫和同侧管的一个基本非交通角的处理的过程中被错过的患者的情况。情况下的20岁女子,孕妇3条第2款的介绍,表现为急性和发烧严重的盆腔疼痛的投诉。骨盆和腹部的多个成像模态显示出8厘米右路盆腔包块与靠近子宫的管状结构。盆腔炎诊断和静脉注射抗生素治疗。审查多个放射图像后,苗勒异常被怀疑,并且与输卵管残角经诊断宫腔镜和腹腔镜证实。随后,进行机器人辅助腹腔镜切除与输卵管右角的。与单角子宫一个基本非交通喇叭的讨论评估可通过几种方法放射学,包括计算机断层扫描,磁共振成像,二和三维超声检查,子宫输卵管造影和宫腔声学造影来实现。此外,伴随骨骼和肾脏异常的评价是在提高诊断的准确性至关重要。在我们的例子中,苗勒异常与迟发并发症被诊断由多个影像学和成功治疗。结论苗勒氏管的早期和正确的诊断仍然是异常困难的,但必要的,因为误诊可与患者严重的并发症有关。

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