A rare childhood uterine malignancy combined with complete uterine inversion.

IF 0.5 Q4 OBSTETRICS & GYNECOLOGY
Lucie Klenovská, Ivana Meixnerová, Luboš Minář, Marta Ježová
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引用次数: 0

Abstract

Objective: An overview of the types of uterine sarcoma, supplemented by an illustrative case report of a rare uterine childhood tumor.

Case report: Our case report describes the case of a 9-year-old girl with a 15-cm tumor in the abdominal cavity, which prolapsed vaginally before introitus during a clinical examination of the abdominal wall causing life-threatening bleeding. This bleeding was stopped by ligation of the tumor pedicle and its resection. Histological examination of the resected specimen described Müllerian adenosarcoma of the uterus. Based on the staging, laparoscopic hysterectomy with bilateral salpingectomy was indicated by the oncogynecological committee. The operation was performed without complications, and intraoperatively, a complete inversion of the uterus was diagnosed.

罕见的儿童子宫恶性肿瘤合并完全子宫内翻。
目的:综述子宫肉瘤的类型,并辅以一例罕见的儿童子宫肿瘤的病例报告。病例报告:我们的病例报告描述了一个9岁的女孩,腹腔有一个15厘米的肿瘤,在临床检查腹壁时,在初次性交前阴道脱垂,导致危及生命的出血。通过结扎肿瘤蒂并切除肿瘤蒂,止血。切除标本的组织学检查描述子宫勒氏腺肉瘤。根据分期,肿瘤妇科委员会建议进行腹腔镜子宫切除术并双侧输卵管切除术。手术无并发症,术中诊断为子宫完全内翻。
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
Ceska Gynekologie-Czech Gynaecology
Ceska Gynekologie-Czech Gynaecology OBSTETRICS & GYNECOLOGY-
CiteScore
0.60
自引率
25.00%
发文量
57
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