Rhabdomyosarcoma-Induced Uterine Inversion.

IF 0.6 Q4 OBSTETRICS & GYNECOLOGY
Case Reports in Obstetrics and Gynecology Pub Date : 2022-07-23 eCollection Date: 2022-01-01 DOI:10.1155/2022/1361803
Kin Li, Gavin Davis, Colleen Wittenberg, Alireza Abidi
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引用次数: 1

Abstract

Nonpuerperal uterine inversion is a rare clinical condition that involves prolapse of the uterine fundus into the uterine cavity and vaginal vault and possibly passed the introitus. The majority of these cases commonly involve benign tumors such as leiomyoma. However, another common cause of nonpuerperal uterine inversion is due to malignancies such as sarcomas. Rhabdomyosarcoma is a rare and aggressive malignancy of soft tissue cells that are common in children and rare in adults. One subtype called embryonal rhabdomyosarcoma is exceptionally rare. Therefore, report of embryonal rhabdomyosarcoma-induced uterine inversion is an exceedingly scarce and rarely documented clinical condition. In this case report, we present a rare case of a nulliparous 27-year-old female who presented with embryonal rhabdomyosarcoma-induced uterine inversion.

Abstract Image

横纹肌肉瘤所致子宫内翻。
非产褥期子宫内翻是一种罕见的临床情况,涉及子宫底脱垂到子宫腔和阴道穹窿,并可能通过子宫内膜。这些病例大多涉及良性肿瘤,如平滑肌瘤。然而,非产褥期子宫内翻的另一个常见原因是恶性肿瘤,如肉瘤。横纹肌肉瘤是一种罕见的侵袭性软组织细胞恶性肿瘤,常见于儿童和罕见的成人。其中一种亚型称为胚胎横纹肌肉瘤,极为罕见。因此,胚胎性横纹肌肉瘤引起子宫内翻的报告是一种非常罕见的临床病例。在这个病例报告中,我们提出一个罕见的27岁未生育女性谁提出胚胎横纹肌肉瘤诱发子宫内翻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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