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dc.contributor.authorLin, Shih-Wenen_US
dc.contributor.authorHsieh, Shu-Weien_US
dc.contributor.authorHuang, Shih-Hungen_US
dc.contributor.authorLiang, Hung-Shuoen_US
dc.contributor.authorHuang, Chia-Yenen_US
dc.date.accessioned2020-01-02T00:04:21Z-
dc.date.available2020-01-02T00:04:21Z-
dc.date.issued2019-11-01en_US
dc.identifier.issn1028-4559en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tjog.2019.09.020en_US
dc.identifier.urihttp://hdl.handle.net/11536/153392-
dc.description.abstractObjective: To report a rare case of endometrial yolk sac tumor (YST) and review published cases of YST of the endometrium. Case report: A 68-year-old female presented with intermittent vaginal spotting for nine months. An endometrial biopsy showed adenocarcinoma. Complete surgical staging operation was performed and the final pathology revealed stage II endometrial yolk sac tumor. The post-operative a-fetoprotein (AFP) level was 133.4 ng/mL. Post-operative adjuvant chemotherapy with bleomycin, etoposide, and cisplatin (BEP) regimen was prescribed for 6 cycles. AFP levels were normal before the fourth cycle of chemotherapy. She is disease free 6 months after completion of therapy. Conclusion: Primary YSTs arising in the endometrium is an extremely rare disease especially in postmenopausal women. Complete surgical staging operation with adjuvant chemotherapy will lead to good outcome in this disease. (C) 2019 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.en_US
dc.language.isoen_USen_US
dc.subjectYolk sac tumoren_US
dc.subjectEndometrial canceren_US
dc.subjectAdjuvant chemotherapyen_US
dc.titleYolk sac tumor of endometrium: A case report and literature reviewen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tjog.2019.09.020en_US
dc.identifier.journalTAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGYen_US
dc.citation.volume58en_US
dc.citation.issue6en_US
dc.citation.spage846en_US
dc.citation.epage848en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000498021000021en_US
dc.citation.woscount0en_US
Appears in Collections:Articles