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首页> 外文期刊>Journal of Medical Case Reports >Degenerated huge retroperitoneal leiomyoma presenting with sonographic features mimicking a large uterine leiomyoma in an infertile woman with a history of myomectomy: a case report
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Degenerated huge retroperitoneal leiomyoma presenting with sonographic features mimicking a large uterine leiomyoma in an infertile woman with a history of myomectomy: a case report

机译:伴有子宫肌瘤切除术史的不育妇女的巨大超声检查样变性的巨大腹膜后平滑肌瘤

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Introduction Retroperitoneal leiomyomata are rare. They are either mistaken preoperatively for malignant retroperitoneal tumors or dealt with as cases of subserous leiomyomata that turn out intraoperatively to be huge retroperitoneal masses of unknown nature. Case presentation We report the case of a 46-year-old nulligravid female patient of Middle Eastern ethnicity who presented to our university hospital with lower abdominal as well as pelvic pain along with a bloated sensation. She also reported noticing an unusual increase in her abdominal girth. These symptoms developed over the previous two months. Preoperative investigation by means of an ultrasound suggested a degenerated subserous huge uterine leiomyoma. An abdominal hysterectomy was planned. Intraoperatively, a normal sized uterus was found, the surface of which was studded with multiple variable sized pedunculated subserous leiomyomata. Another huge retroperitoneal soft to firm mass was found extending from her left pelvic wall to the level of her spleen, with no connections to her uterus. The mass was excised and a histopathological examination revealed a degenerated leiomyoma. Conclusion Some unusually located extra-uterine leiomyomata have been reported; retroperitoneal leiomyoma being among them. The origin of such tumors is still obscure; a parasitic origin as well as Müllerian cell rests or smooth muscle cells in the retroperitoneal vessels wall have been suggested. An 'iatrogenic' origin for such growths is also a possible theory. The origin of uncommonly located leiomyomata is an unexplored issue that merits more investigation.
机译:引言腹膜后平滑肌瘤很少见。他们或者在术前被误认为是恶性腹膜后肿瘤,或者被当作浆液性平滑肌瘤的病例处理,这些病例在术中发现是性质未知的巨大腹膜后肿块。病例介绍我们报告了一位46岁的中东种族零重力女性患者的病例,该患者出现在我们的大学医院,腹部下垂,骨盆疼痛伴有腹胀感。她还报告注意到腹围异常增加。这些症状在前两个月出现。术前超声检查提示变性的浆液性巨大子宫平滑肌瘤。计划进行腹部子宫切除术。术中发现一个正常大小的子宫,其表面布满了多个可变大小的有蒂的浆液性平滑肌瘤。发现另一个巨大的腹膜后软组织到硬块,从左骨盆壁一直延伸到脾水平,与子宫没有任何联系。切下肿块,组织病理学检查发现变性肌瘤。结论已有报道子宫外平滑肌瘤位置异常。腹膜后平滑肌瘤就在其中。此类肿瘤的起源仍不清楚。已经提出了寄生起源以及腹膜后血管壁中的苗勒氏细胞静止或平滑肌细胞。这种生长的“医源性”起源也是一种可能的理论。罕见的平滑肌瘤的起源是一个尚待探讨的问题,值得进一步研究。

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