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Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature
An epithelioid trophoblastic tumor (ETT) is a rare trophoblastic tumor originating from chorionic-type intermediate trophoblasts. Vaginal involvement in ETT in the form of isolated lesions has not been previously reported. A 43-year-old woman presented with vaginal wall cysts and was diagnosed with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814932/ https://www.ncbi.nlm.nih.gov/pubmed/24194644 http://dx.doi.org/10.2147/OTT.S50553 |
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author | Zhao, Jing Xiang, Yang Zhao, Dachun Ren, Tong Feng, Fengzhi Wan, Xirun |
author_facet | Zhao, Jing Xiang, Yang Zhao, Dachun Ren, Tong Feng, Fengzhi Wan, Xirun |
author_sort | Zhao, Jing |
collection | PubMed |
description | An epithelioid trophoblastic tumor (ETT) is a rare trophoblastic tumor originating from chorionic-type intermediate trophoblasts. Vaginal involvement in ETT in the form of isolated lesions has not been previously reported. A 43-year-old woman presented with vaginal wall cysts and was diagnosed with ETT by pathological examination after cystectomy. No clinical evidence of uterine involvement was found at diagnosis or during follow-up. The patient was treated with chemotherapy and surgery after the first recurrence and underwent follow-up for 8 months. The serum human chorionic gonadotropin titer remained at undetectable levels. |
format | Online Article Text |
id | pubmed-3814932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38149322013-11-05 Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature Zhao, Jing Xiang, Yang Zhao, Dachun Ren, Tong Feng, Fengzhi Wan, Xirun Onco Targets Ther Case Report An epithelioid trophoblastic tumor (ETT) is a rare trophoblastic tumor originating from chorionic-type intermediate trophoblasts. Vaginal involvement in ETT in the form of isolated lesions has not been previously reported. A 43-year-old woman presented with vaginal wall cysts and was diagnosed with ETT by pathological examination after cystectomy. No clinical evidence of uterine involvement was found at diagnosis or during follow-up. The patient was treated with chemotherapy and surgery after the first recurrence and underwent follow-up for 8 months. The serum human chorionic gonadotropin titer remained at undetectable levels. Dove Medical Press 2013-10-29 /pmc/articles/PMC3814932/ /pubmed/24194644 http://dx.doi.org/10.2147/OTT.S50553 Text en © 2013 Zhao et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Zhao, Jing Xiang, Yang Zhao, Dachun Ren, Tong Feng, Fengzhi Wan, Xirun Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
title | Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
title_full | Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
title_fullStr | Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
title_full_unstemmed | Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
title_short | Isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
title_sort | isolated epithelioid trophoblastic tumor of the vagina: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814932/ https://www.ncbi.nlm.nih.gov/pubmed/24194644 http://dx.doi.org/10.2147/OTT.S50553 |
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