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首页> 外文期刊>Journal of International Medical Research >Giant hysteromyoma after vaginoplasty in a woman with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: case report and review of the literature
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Giant hysteromyoma after vaginoplasty in a woman with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: case report and review of the literature

机译：阴道成形术后的巨型毒蕈瘤在一个妇女的妇女综合征：案例报告和审查文献中

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摘要

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder characterized by congenital absence of both the uterus and vagina. Some patients require surgery to create a neovagina, however, the preservation of a nonfunctional rudimentary uterus after surgery may lead to long-term complications. Herein, a rare case of a giant hysteromyoma after vaginoplasty, in a 31-year-old Chinese female patient who was diagnosed with MRKH syndrome, is reported. The patient, who had undergone vaginal reconstruction 4 years previously, presented with abdominal distension for the previous 2 weeks. Transabdominal ultrasonography showed a firm mass of approximately 10?×?10?cm in the lower abdomen. The patient subsequently underwent an exploratory laparotomy, and a leiomyoma from her rudimentary uterus was removed. Beside this case, seven cases, published between 2004 and 2020, were identified during a literature search. Findings of the present and previously published cases suggest that gynaecologists should pay particular attention to the risks of pelvic complications in female patients with MRKH syndrome who have previously undergone surgery, and select appropriate therapeutic methods.
机译：Mayer-Rokitansky-küster-hauser（MRKH）综合征是先天性疾病，其特征在于先天性缺乏子宫和阴道。一些患者需要手术以产生新奥诺那，然而，手术后的无功能基本子宫可能导致长期并发症。据报道，据报道，在阴道成形术后，在诊断综合征诊断的31岁的中国女性患者中，罕见的呼吸道肌瘤。患者在前期2周内患有4年的阴道重建，患有腹胀。 TransaboMinal超声检查显示在下腹部约为10Ω×10Ω厘米的牢固质量。患者随后接受了探索性剖腹手术，并除去了来自她的基本子宫的平滑肌瘤。在这种情况下，在文献搜索期间识别了7个案例，发表于2004年至2020年。目前和以前公布的案例表明，妇科医生应特别注意女性患者的骨盆并发症的风险，患有以前经历过手术的MRKH综合征，并选择适当的治疗方法。

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