A Case Report of Bilateral Endometrioid-Type Ovarian Carcinoma with Synchronous Dual Metastasis to the Colon

W. T. N. Widanage, K. S. Nathawitharanalage, N. A. Kodithuwakku, A. A. S. Samarathunga, H. M. S. P. Rajaguru, K. P. Dissanayake, L. R. A. Wijesooriya, J. A. S. B. Jayasundara
{"title":"A Case Report of Bilateral Endometrioid-Type Ovarian Carcinoma with Synchronous Dual Metastasis to the Colon","authors":"W. T. N. Widanage, K. S. Nathawitharanalage, N. A. Kodithuwakku, A. A. S. Samarathunga, H. M. S. P. Rajaguru, K. P. Dissanayake, L. R. A. Wijesooriya, J. A. S. B. Jayasundara","doi":"10.1007/s42399-024-01638-w","DOIUrl":null,"url":null,"abstract":"<p>Despite primary colorectal cancer being the third frequent malignancy worldwide, secondary metastasis to the large bowel from another primary cancer is seldom reported. Only a handful of previous cases of primary ovarian cancer metastasizing to the large bowel have been described in literature published in English up to date. We report a case of bilateral ovarian carcinoma with synchronous dual metastasis to the left colon, probably the first report of such nature. A 56-year-old Sri Lankan female presented with left-sided non-specific abdominal pain for 2 months. She was found to have bilateral ovarian tumours with elevated serum CA 125 levels, and near-occluding splenic flexure and descending colon masses. The patient underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, left hemicolectomy with regional lymph node dissection and omentectomy. Histology confirmed endometrioid adenocarcinoma of both ovaries with metastatic deposits in both colonic masses and in two out of seven lymph nodes along the left colic vascular pedicle. Both ovarian tumours and both colonic deposits were positively stained for ER and vimentin, and were negative for CK20 on immunohistochemistry indicating ovarian origin. The patient was disease-free at 2 years from the uncomplicated primary surgery having completed adjuvant chemotherapy. This case highlights the importance of the clinicians to be mindful of rare occurrences of large bowel secondary deposits of ovarian origin, especially when patients present with simultaneous large bowel and adnexal masses. Upfront bowel resection than neoadjuvant therapy could be performed safely in cases with impending bowel obstruction with satisfactory outcome.</p>","PeriodicalId":21944,"journal":{"name":"SN Comprehensive Clinical Medicine","volume":"50 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"SN Comprehensive Clinical Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s42399-024-01638-w","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

Despite primary colorectal cancer being the third frequent malignancy worldwide, secondary metastasis to the large bowel from another primary cancer is seldom reported. Only a handful of previous cases of primary ovarian cancer metastasizing to the large bowel have been described in literature published in English up to date. We report a case of bilateral ovarian carcinoma with synchronous dual metastasis to the left colon, probably the first report of such nature. A 56-year-old Sri Lankan female presented with left-sided non-specific abdominal pain for 2 months. She was found to have bilateral ovarian tumours with elevated serum CA 125 levels, and near-occluding splenic flexure and descending colon masses. The patient underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, left hemicolectomy with regional lymph node dissection and omentectomy. Histology confirmed endometrioid adenocarcinoma of both ovaries with metastatic deposits in both colonic masses and in two out of seven lymph nodes along the left colic vascular pedicle. Both ovarian tumours and both colonic deposits were positively stained for ER and vimentin, and were negative for CK20 on immunohistochemistry indicating ovarian origin. The patient was disease-free at 2 years from the uncomplicated primary surgery having completed adjuvant chemotherapy. This case highlights the importance of the clinicians to be mindful of rare occurrences of large bowel secondary deposits of ovarian origin, especially when patients present with simultaneous large bowel and adnexal masses. Upfront bowel resection than neoadjuvant therapy could be performed safely in cases with impending bowel obstruction with satisfactory outcome.

Abstract Image

双侧子宫内膜样卵巢癌同步双转移至结肠的病例报告
尽管原发性大肠癌是全球第三大常见恶性肿瘤,但很少有报道称另一种原发性癌症继发转移至大肠。迄今为止,英文文献中关于原发性卵巢癌转移至大肠的报道屈指可数。我们报告了一例双侧卵巢癌同步双转移至左侧结肠的病例,这可能是首例此类病例。一名 56 岁的斯里兰卡女性因左侧非特异性腹痛就诊 2 个月。她被发现患有双侧卵巢肿瘤,血清 CA 125 水平升高,脾曲和降结肠肿块几乎包括在内。患者接受了全腹子宫切除术、双侧输卵管切除术、左半结肠切除术和区域淋巴结清扫术以及卵巢切除术。组织学证实,双侧卵巢均为子宫内膜样腺癌,双侧结肠肿块和左侧结肠血管蒂的七个淋巴结中有两个出现转移沉积。两个卵巢肿瘤和两个结肠沉积物的ER和波形蛋白均呈阳性染色,免疫组化结果显示CK20阴性,表明肿瘤来源于卵巢。该患者在完成辅助化疗后,进行了简单的初次手术,术后两年未再发病。本病例强调了临床医生注意罕见的卵巢源性大肠继发性沉积物的重要性,尤其是当患者同时伴有大肠和附件肿块时。对于即将发生肠梗阻的病例,可以先行肠道切除术,然后再进行新辅助治疗,这样可以安全地达到满意的疗效。
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
自引率
0.00%
发文量
0
×
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