{"title":"Mixed Endometrioid Clear Cell Carcinoma of the Ovary: A Case Report","authors":"M. Esmaeilpour, M. Hasanzadeh, Mrayam Mohammadi","doi":"10.2174/1573404820666230504101534","DOIUrl":null,"url":null,"abstract":"\n\nDespite the high percentage of pure forms of epithelial ovarian cancers\n(EOC), mixed epithelial cancer of the ovary is extremely rare and accounts for less than 1% percent of\nall epithelial ovarian cancers. Because of the low prevalence; there are only a few cases of mixed epithelial cancers published in the literature. This study presents the case of a mixed endometrioid\n(EC)/clear cell carcinoma (CCC), diagnosed in a woman with a complaint of low back pain and a history of infertility.\n\n\n\nWe report the case of a 35-year-old woman who came to our clinic complaining of progressive back pain and a history of infertility. Imaging showed a left ovarian mass that was compatible\nwith malignant tumors. The patient underwent open surgery and a frozen section evaluation of the tumor was done during the operation. The pathology result demonstrated mixed CCC/EC histology in\nthe left ovary. We decided to perform a total abdominal hysterectomy as well as right salpingooophorectomy, omentectomy, bilateral pelvic lymphadenectomy, and para-aortic lymphadenectomy.\nAdjuvant chemotherapy was administrated postoperatively.\n\n\n\nAlthough epithelial cancers account for more than 90% of all ovarian cancers (OC), developing mixed forms of epithelial cancers is extremely rare, and there are little data available in the\nliterature about their presentation and histopathological features. The main purpose of this article was\nto report a mixed CCC/EC and to discuss different aspects of this rare histologic type of OC. More research is needed to determine metastatic potential as well as the likelihood of recurrence of these\nunique neoplasms.\n","PeriodicalId":371340,"journal":{"name":"Current Womens Health Reviews","volume":"62 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Womens Health Reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1573404820666230504101534","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 the high percentage of pure forms of epithelial ovarian cancers
(EOC), mixed epithelial cancer of the ovary is extremely rare and accounts for less than 1% percent of
all epithelial ovarian cancers. Because of the low prevalence; there are only a few cases of mixed epithelial cancers published in the literature. This study presents the case of a mixed endometrioid
(EC)/clear cell carcinoma (CCC), diagnosed in a woman with a complaint of low back pain and a history of infertility.
We report the case of a 35-year-old woman who came to our clinic complaining of progressive back pain and a history of infertility. Imaging showed a left ovarian mass that was compatible
with malignant tumors. The patient underwent open surgery and a frozen section evaluation of the tumor was done during the operation. The pathology result demonstrated mixed CCC/EC histology in
the left ovary. We decided to perform a total abdominal hysterectomy as well as right salpingooophorectomy, omentectomy, bilateral pelvic lymphadenectomy, and para-aortic lymphadenectomy.
Adjuvant chemotherapy was administrated postoperatively.
Although epithelial cancers account for more than 90% of all ovarian cancers (OC), developing mixed forms of epithelial cancers is extremely rare, and there are little data available in the
literature about their presentation and histopathological features. The main purpose of this article was
to report a mixed CCC/EC and to discuss different aspects of this rare histologic type of OC. More research is needed to determine metastatic potential as well as the likelihood of recurrence of these
unique neoplasms.