Low mitotic count may affect the prognosis of uterine leiomyosarcoma: A report of two cases

IF 1.2 Q3 OBSTETRICS & GYNECOLOGY
Christine Cho , Ciara Marshall , Erik Washburn , Edward Podczaski , Joel Sorosky , Shaina Bruce
{"title":"Low mitotic count may affect the prognosis of uterine leiomyosarcoma: A report of two cases","authors":"Christine Cho ,&nbsp;Ciara Marshall ,&nbsp;Erik Washburn ,&nbsp;Edward Podczaski ,&nbsp;Joel Sorosky ,&nbsp;Shaina Bruce","doi":"10.1016/j.gore.2025.101766","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Uterine leiomyosarcoma (uLMS) is characterized by its aggressive nature, early metastatic potential, and poor clinical outcomes. Diagnosis of uLMS requires two out of the following three diagnostic criteria: marked cytologic atypia, 10 mitoses per 10 high power fields, tumor cell necrosis. This case series presents two cases of uLMS with a low mitotic rate and an indolent disease course, with excellent response to hormone therapies.</div></div><div><h3>Case 1</h3><div>A 44-year-old female was diagnosed with uLMS following a supracervical hysterectomy in 2006. The primary tumor demonstrated tumor cell necrosis, cytologic atypic, and 6 mitoses per 10 HPF. Her 18-year disease course is notable for four debulking surgeries and multiple courses of hormonal therapy resulting in durable responses.</div></div><div><h3>Case 2</h3><div>A 75-year-old female was diagnosed with smooth muscle tumor of uncertain malignant potential (STUMP) status post debulking surgery which was revised to leiomyosarcoma following lung biopsy confirmation of metastasis. The primary tumor and lung biopsy demonstrated tumor cell necrosis, cytologic atypia and 2 mitosis per 10 HPF. She demonstrated stable disease on letrozole for 11 months.</div></div><div><h3>Discussion</h3><div>These cases demonstrate that uLMS with low mitotic activity may exhibit less aggressive behavior than typical high-grade sarcomas. Recognizing this distinction can guide prognostication and treatment selection.</div></div>","PeriodicalId":12873,"journal":{"name":"Gynecologic Oncology Reports","volume":"59 ","pages":"Article 101766"},"PeriodicalIF":1.2000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gynecologic Oncology Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352578925000918","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Uterine leiomyosarcoma (uLMS) is characterized by its aggressive nature, early metastatic potential, and poor clinical outcomes. Diagnosis of uLMS requires two out of the following three diagnostic criteria: marked cytologic atypia, 10 mitoses per 10 high power fields, tumor cell necrosis. This case series presents two cases of uLMS with a low mitotic rate and an indolent disease course, with excellent response to hormone therapies.

Case 1

A 44-year-old female was diagnosed with uLMS following a supracervical hysterectomy in 2006. The primary tumor demonstrated tumor cell necrosis, cytologic atypic, and 6 mitoses per 10 HPF. Her 18-year disease course is notable for four debulking surgeries and multiple courses of hormonal therapy resulting in durable responses.

Case 2

A 75-year-old female was diagnosed with smooth muscle tumor of uncertain malignant potential (STUMP) status post debulking surgery which was revised to leiomyosarcoma following lung biopsy confirmation of metastasis. The primary tumor and lung biopsy demonstrated tumor cell necrosis, cytologic atypia and 2 mitosis per 10 HPF. She demonstrated stable disease on letrozole for 11 months.

Discussion

These cases demonstrate that uLMS with low mitotic activity may exhibit less aggressive behavior than typical high-grade sarcomas. Recognizing this distinction can guide prognostication and treatment selection.
低有丝分裂计数可能影响子宫平滑肌肉瘤的预后:附2例报告
子宫平滑肌肉瘤(uLMS)具有侵袭性、早期转移潜力和临床预后差的特点。诊断uLMS需要以下三个诊断标准中的两个:明显的细胞学非典型性,每10个高倍视野10次有丝分裂,肿瘤细胞坏死。本病例系列介绍两例uLMS,有丝分裂率低,病程缓慢,对激素治疗反应良好。病例1A, 44岁女性,于2006年行宫颈上子宫切除术后被诊断为uLMS。原发肿瘤表现为肿瘤细胞坏死,细胞学不典型,每10 HPF有6个有丝分裂。她在18年的病程中因四次减脂手术和多次激素治疗而引起持久的反应。病例2A, 75岁女性,术后诊断为平滑肌肿瘤(STUMP)状态不确定,肺活检证实转移后改为平滑肌肉瘤。原发肿瘤和肺活检显示肿瘤细胞坏死,细胞学异型性和每10 HPF 2个有丝分裂。她在来曲唑治疗11个月后病情稳定。这些病例表明,有丝分裂活性低的uLMS可能比典型的高级别肉瘤表现出更少的侵袭性行为。认识到这一区别可以指导预后和治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Gynecologic Oncology Reports
Gynecologic Oncology Reports OBSTETRICS & GYNECOLOGY-
CiteScore
2.00
自引率
0.00%
发文量
183
审稿时长
41 days
期刊介绍: Gynecologic Oncology Reports is an online-only, open access journal devoted to the rapid publication of narrative review articles, survey articles, case reports, case series, letters to the editor regarding previously published manuscripts and other short communications in the field of gynecologic oncology. The journal will consider papers that concern tumors of the female reproductive tract, with originality, quality, and clarity the chief criteria of acceptance.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信