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Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature

Epithelioid trophoblastic tumor (ETT) is a rare gestational trophoblastic tumor. Cases of ETT present as abnormal vaginal bleeding in women of reproductive age, with low human chorionic gonadotropin (hCG) levels. ETT can be a sequela of any gestational event and can present in both intrauterine and...

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Autores principales: Scott, Eirwen M., Smith, Ashlee L., Desouki, Mohamed Mokhtar, Olawaiye, Alexander B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518084/
https://www.ncbi.nlm.nih.gov/pubmed/23243530
http://dx.doi.org/10.1155/2012/862472
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author Scott, Eirwen M.
Smith, Ashlee L.
Desouki, Mohamed Mokhtar
Olawaiye, Alexander B.
author_facet Scott, Eirwen M.
Smith, Ashlee L.
Desouki, Mohamed Mokhtar
Olawaiye, Alexander B.
author_sort Scott, Eirwen M.
collection PubMed
description Epithelioid trophoblastic tumor (ETT) is a rare gestational trophoblastic tumor. Cases of ETT present as abnormal vaginal bleeding in women of reproductive age, with low human chorionic gonadotropin (hCG) levels. ETT can be a sequela of any gestational event and can present in both intrauterine and extrauterine sites. Metastasis and death have been reported. We present a case of a 44-year-old female incidentally diagnosed with ETT following laparoscopic-assisted vaginal hysterectomy. Postoperative evaluation for metastatic disease was negative. The patient has been closely followed and remains disease free 8 months postoperatively. ETT presents a diagnostic challenge due to its rarity and histologic resemblance to other pathologies. ETT is relatively chemoresistant and managed surgically. Misdiagnosis delays effective treatment and affects survival.
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spelling pubmed-35180842012-12-14 Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature Scott, Eirwen M. Smith, Ashlee L. Desouki, Mohamed Mokhtar Olawaiye, Alexander B. Case Rep Obstet Gynecol Case Report Epithelioid trophoblastic tumor (ETT) is a rare gestational trophoblastic tumor. Cases of ETT present as abnormal vaginal bleeding in women of reproductive age, with low human chorionic gonadotropin (hCG) levels. ETT can be a sequela of any gestational event and can present in both intrauterine and extrauterine sites. Metastasis and death have been reported. We present a case of a 44-year-old female incidentally diagnosed with ETT following laparoscopic-assisted vaginal hysterectomy. Postoperative evaluation for metastatic disease was negative. The patient has been closely followed and remains disease free 8 months postoperatively. ETT presents a diagnostic challenge due to its rarity and histologic resemblance to other pathologies. ETT is relatively chemoresistant and managed surgically. Misdiagnosis delays effective treatment and affects survival. Hindawi Publishing Corporation 2012 2012-12-02 /pmc/articles/PMC3518084/ /pubmed/23243530 http://dx.doi.org/10.1155/2012/862472 Text en Copyright © 2012 Eirwen M. Scott et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Scott, Eirwen M.
Smith, Ashlee L.
Desouki, Mohamed Mokhtar
Olawaiye, Alexander B.
Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature
title Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature
title_full Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature
title_fullStr Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature
title_full_unstemmed Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature
title_short Epithelioid Trophoblastic Tumor: A Case Report and Review of the Literature
title_sort epithelioid trophoblastic tumor: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518084/
https://www.ncbi.nlm.nih.gov/pubmed/23243530
http://dx.doi.org/10.1155/2012/862472
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