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Clear cell ovarian adenocarcinoma
Journal of Surgical Oncology
|December 1, 1984
Summary
Clear cell ovarian carcinoma is rare in women under 40. This study analyzes 22 cases, noting associations with endometriosis and endometrial cancer, and discusses treatment responses.
Area of Science:
- Gynecologic Oncology
- Pathology
- Medical Oncology
Background:
- Clear cell ovarian carcinoma (CCOC) is a rare subtype of epithelial ovarian cancer.
- It predominantly affects postmenopausal women, with rarity below age 40 reaffirmed.
- CCOC exhibits distinct clinicopathologic features and treatment challenges.
Purpose of the Study:
- To analyze the clinicopathologic features of 22 CCOC cases.
- To review the literature on CCOC, focusing on rarity, associations, and outcomes.
- To outline a management plan for CCOC.
Main Methods:
- Retrospective analysis of 22 patient cases.
- Literature survey of previously reported CCOC cases.
- Review of clinical, pathological, and treatment data.
Main Results:
- Rarity of CCOC in patients under 40 confirmed.
- Observed hypercalcemia (2 patients) and thromboembolic complications (3 patients).
- Coexistent endometriosis (10 patients, 26% in literature) and endometrial carcinoma (2 patients, 14% in literature) noted.
- Poor survival for Stage III/IV disease (0% vs. 8% in literature).
- Suggestive radiation response in Stage IIC disease; partial responses to chemotherapy (adriamycin, cytoxan, cis-platinum).
Conclusions:
- CCOC is rare in premenopausal women.
- CCOC has significant associations with endometriosis and endometrial carcinoma.
- Advanced stage disease carries a poor prognosis; chemotherapy and radiotherapy show potential therapeutic benefits.