Publication details

Raritní děložní malignita dětského věku kombinovaná s kompletní inverzí dělohy

Title in English A rare childhood uterine malignancy combined with complete uterine inversion
Authors

KLENOVSKÁ Lucie MEIXNEROVÁ Ivana MINÁŘ Luboš JEŽOVÁ Marta

Year of publication 2025
Type Article in Periodical
Magazine / Source Česká gynekologie
MU Faculty or unit

Faculty of Medicine

Citation
Doi http://dx.doi.org/10.48095/cccg20251
Keywords uterine sarcoma; leiomyosarcoma; endometrial stromal sarcoma; Müllerian adenosarcoma; uterine inversion
Description 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.

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