An occult leiomyosarcoma in a hysterectomy specimen presumed to be uterine fibroid preoperatively: A case report

Swati Priya, S. Mahto, M. K. Paswan, Saurav Banerjee, Arvind Kumar
{"title":"An occult leiomyosarcoma in a hysterectomy specimen presumed to be uterine fibroid preoperatively: A case report","authors":"Swati Priya, S. Mahto, M. K. Paswan, Saurav Banerjee, Arvind Kumar","doi":"10.18231/j.ijpo.2024.017","DOIUrl":null,"url":null,"abstract":"Uterine sarcomas account for approximately 1% of all gynecologic neoplasm and 3–7% of all uterine cancers. Approximately 1 in every 800 women believed to have a leiomyoma actually has a sarcoma. Here we discuss a case of occult leiomyosarcoma in a hysterectomy specimen suspected to be uterine fibroid preoperatively along with spectrum of diagnoses of uterine mesenchymal tumours and the differentiating parameters. This is a descriptive study. A 48-year-old female with heavy menstrual bleeding since 4-5 years, on USG showed an enlarged uterus containing a fibroid with degenerative changes. Grossly, fibroid is seen (11cm x 8.6cm) greyish white, fleshy, involving more than half of the myometrium. Microscopically, fibroid mass showed highly pleomorphic, hyperchromatic tumour cells with dispersed chromatin and indistinct cytoplasm, arranged in intersecting fascicles. Large areas of coagulative tumour cell necrosis seen, mitotic figures > 10 per 10 HPF, suggesting leiomysarcoma of uterus. Leiomyosarcomas are diagnosed when a triad of histopathological features is seen - significant atypia, increased mitotic activity and coagulative tumour cell necrosis. These are important in differentiating between variants of leiomyoma, STUMP and leiomyosarcoma. Sometimes a benign fibroid-like mass can incidentally be diagnosed as leiomyosarcoma microscopically. It’s essential to avertmorcellation in routine gynecological practice especially in perimenopausal women with a large fibroid to avoid intra-abdominal dissemination. Precise pre-operative radiological workup by MRI or expert-guided sonogram is also suggested but given the complexities involved, role of histopathology to diagnose leiomyosarcoma is invaluable.","PeriodicalId":486471,"journal":{"name":"Indian Journal of Pathology and Oncology","volume":"11 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Pathology and Oncology","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.18231/j.ijpo.2024.017","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Uterine sarcomas account for approximately 1% of all gynecologic neoplasm and 3–7% of all uterine cancers. Approximately 1 in every 800 women believed to have a leiomyoma actually has a sarcoma. Here we discuss a case of occult leiomyosarcoma in a hysterectomy specimen suspected to be uterine fibroid preoperatively along with spectrum of diagnoses of uterine mesenchymal tumours and the differentiating parameters. This is a descriptive study. A 48-year-old female with heavy menstrual bleeding since 4-5 years, on USG showed an enlarged uterus containing a fibroid with degenerative changes. Grossly, fibroid is seen (11cm x 8.6cm) greyish white, fleshy, involving more than half of the myometrium. Microscopically, fibroid mass showed highly pleomorphic, hyperchromatic tumour cells with dispersed chromatin and indistinct cytoplasm, arranged in intersecting fascicles. Large areas of coagulative tumour cell necrosis seen, mitotic figures > 10 per 10 HPF, suggesting leiomysarcoma of uterus. Leiomyosarcomas are diagnosed when a triad of histopathological features is seen - significant atypia, increased mitotic activity and coagulative tumour cell necrosis. These are important in differentiating between variants of leiomyoma, STUMP and leiomyosarcoma. Sometimes a benign fibroid-like mass can incidentally be diagnosed as leiomyosarcoma microscopically. It’s essential to avertmorcellation in routine gynecological practice especially in perimenopausal women with a large fibroid to avoid intra-abdominal dissemination. Precise pre-operative radiological workup by MRI or expert-guided sonogram is also suggested but given the complexities involved, role of histopathology to diagnose leiomyosarcoma is invaluable.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
术前推测为子宫肌瘤的子宫切除术标本中的隐匿性子宫肌瘤:病例报告
子宫肉瘤约占所有妇科肿瘤的 1%,占所有子宫癌的 3-7%。大约每 800 名被认为患有子宫肌瘤的妇女中就有 1 人实际上患有肉瘤。在此,我们将讨论一例术前被怀疑为子宫肌瘤的子宫切除标本中的隐匿性子宫肌瘤,以及子宫间质瘤的诊断范围和鉴别参数。这是一项描述性研究。一名 48 岁的女性自 4-5 年前开始大量月经出血,USG 显示子宫增大,内含一个伴有退行性病变的肌瘤。大体可见肌瘤(11 厘米 x 8.6 厘米)灰白色,肉质,累及一半以上的子宫肌层。显微镜下,子宫肌瘤肿块显示出高度多形性、高色素的肿瘤细胞,染色质分散,胞浆不清,呈交叉束状排列。可见大面积凝固性瘤细胞坏死,每 10 HPF 有丝分裂数大于 10,提示为子宫线粒体肉瘤。当组织病理学特征出现三联征时,即明显不典型性、有丝分裂活性增强和凝集性肿瘤细胞坏死,即可诊断为子宫线肉瘤。这些特征对于鉴别变异型子宫肌瘤、STUMP 和子宫肌瘤非常重要。有时,良性纤维瘤样肿块在显微镜下可偶然诊断为子宫肌瘤。在常规妇科手术中,尤其是围绝经期妇女的巨大子宫肌瘤必须避免切除,以避免腹腔内播散。此外,还建议术前通过核磁共振成像或专家指导的超声波检查进行精确的放射学检查,但鉴于其中的复杂性,组织病理学在诊断子宫肌瘤中的作用非常重要。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Mucinous cystic neoplasm of the liver: A rare case report A primary leiomyosarcoma of small intestine: A rare case report Metastatic GIST with a TWIST of RCC: A case report Demographic profile of thyroid malignancies in a tertiary care centre in South India Primary ovarian squamous cell carcinoma arising from an epidermoid cyst of Ovary- A rare case report with review of literature
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1