Woman's Health Sciences Department, Gynecologic Section, Polytechnic University of Marche, Ancona, Italy.
Woman's Health Sciences Department, Gynecologic Section, Polytechnic University of Marche, Ancona, Italy.
Fertil Steril. 2024 Nov;122(5):948-950. doi: 10.1016/j.fertnstert.2024.07.034. Epub 2024 Jul 27.
To report a rare, misleading fibroid degeneration involving a nonfunctional, noncommunicating horn in a woman with a unicornuate uterus. Although the presence of a functional rudimentary horn may lead to signs and symptoms that recommend its removal, nonfunctional cases are rarely reported, and because of their apparent functional inactivity, the need for their removal has not yet been reported. No previous report showed the possibility of a degenerative process in a nonfunctional rudimentary horn causing patient discomfort.
This is a step-by-step narrated video showing a unique case of fibroid degeneration and growth of a nonfunctional, noncommunicating rudimentary horn in a unicornuate uterus (American Society for Reproductive Medicine classification 2021) and its surgical management.
University academic hospital.
PATIENT(S): A 48-year-old White nulliparous premenopausal woman was referred to our institution because of abdominal pain and an enlarging adnexal mass. Her personal history showed primary infertility with a previous diagnosis of unicornuate uterus. Given the possibility of ectopic ureters in these occurrences, complete computed tomography was performed, and no genitourinary alterations were found. Preoperative imaging (ultrasound evaluation, computed tomography, and magnetic resonance imaging) provided a provisional diagnosis of a suspicious ovarian fibroma.
INTERVENTION(S): Considering the patient's age, lack of desire for pregnancy, and volumetric increase in the adnexal mass, a laparoscopic intervention to perform mass removal and prophylactic bilateral salpingectomy was planned. The patient was counseled about the low risk of an underlying malignant transformation. Therefore, the decision to remove the intact mass via a minilaparotomy at the end of the surgery was shared. Once the abdominal cavity was entered, the right unicornuate uterus was found in anatomical continuity with the ipsilateral broad ligament, fallopian tube, and ovary. These structures were wholly attached to the right pelvic wall. On the other side, cranially compared with the right hemiuterus, a roundish myoma-like mass was detected in direct connection with the left broad ligament, fallopian tube, and ovary. In light of a changed intraoperative finding, amputation of the left rudimentary horn and prophylactic bilateral salpingectomy were performed.
MAIN OUTCOME MEASURE(S): Showing the fibroid degeneration and growth of a nonfunctional, noncommunicating rudimentary horn in a unicornuate uterus (American Society for Reproductive Medicine classification 2021) treated laparoscopically.
RESULT(S): Laparoscopic removal of the uterine horn was successful, and no intraoperative and postoperative complications occurred. The patient was in good health at the 6-month follow-up visit. The histopathological examination confirmed the fibroid degeneration and absence of the endometrium.
CONCLUSION(S): The lack of symptomatic cases of rudimentary nonfunctional horns reported in the literature led gynecologists to consider them a silent Müllerian anomaly. This unique case demonstrates that even nonfunctional rudimentary horns can undergo symptomatic transformation processes requiring surgery. This information may be helpful for more comprehensive counseling of women and for considering the possibility of this occurrence in the diagnostic workup of misleading Müllerian anomalies. With this in mind, surgical treatment can also be better planned as the technical aspects change compared with what is expected for an adnexal pathology.
报告一例罕见的、具有误导性的子宫肌瘤变性,涉及具有单侧子宫的非功能性、非交通性残角子宫。虽然功能性残角子宫可能会出现导致其切除的体征和症状,但非功能性病例很少见报道,而且由于其明显的功能不活跃,其切除的必要性尚未被报道。以前没有报告表明,非功能性残角子宫的退行性过程会导致患者不适。
这是一个分步叙述的视频,展示了一例单侧子宫(美国生殖医学学会 2021 年分类)中罕见的子宫肌瘤变性和非功能性、非交通性残角子宫的生长及其手术处理。
大学学术医院。
一位 48 岁的白人未产绝经前妇女因腹痛和附件肿块增大而被转至我院。她的个人史显示原发性不孕,此前诊断为单侧子宫。鉴于这些情况下可能存在异位输尿管,因此进行了全面的计算机断层扫描,未发现泌尿生殖系统改变。术前影像学(超声评估、计算机断层扫描和磁共振成像)提供了可疑卵巢纤维瘤的初步诊断。
鉴于患者年龄、缺乏妊娠愿望以及附件肿块体积增大,计划进行腹腔镜手术切除肿块和预防性双侧输卵管切除术。对患者进行了低恶性转化风险的咨询。因此,分享了通过手术结束时的小切口完整切除肿块的决策。一旦进入腹腔,就发现右侧单侧子宫与同侧阔韧带、输卵管和卵巢在解剖学上连续。这些结构完全附着在右侧骨盆壁上。在另一侧,与右侧半子宫相比,在颅侧发现了一个圆形肌瘤样肿块,直接与左侧阔韧带、输卵管和卵巢相连。根据术中改变的发现,行左侧残角子宫切除术和预防性双侧输卵管切除术。
展示单侧子宫(美国生殖医学学会 2021 年分类)中罕见的子宫肌瘤变性和非功能性、非交通性残角子宫的生长,并经腹腔镜治疗。
腹腔镜切除子宫角成功,无术中及术后并发症发生。患者在 6 个月的随访时身体状况良好。组织病理学检查证实为子宫肌瘤变性和无子宫内膜。
文献中报道的无症状的非功能性残角子宫病例较少,这导致妇科医生认为它们是一种沉默的 Müllerian 异常。这个独特的病例表明,即使是非功能性的残角子宫也可能发生需要手术的有症状的转化过程。这一信息可能有助于对女性进行更全面的咨询,并考虑在误导性 Müllerian 异常的诊断工作中出现这种情况的可能性。考虑到这一点,与预期的附件病变相比,手术技术方面的变化可能会更好地规划手术治疗。