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Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention

BACKGROUND: Gestational trophoblastic disease (GTD) is a rare developmental form of proliferative trophoblastic tissue. Sparse literature exists regarding the optimal management of patients with advanced GTD, but the definitive treatment is urgent surgical intervention. CASE: A 48-year-old woman pre...

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Detalles Bibliográficos
Autores principales: Lehto, Ann, Hitscherich, Kyle, Argeros, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111126/
https://www.ncbi.nlm.nih.gov/pubmed/30167379
http://dx.doi.org/10.1016/j.crwh.2018.e00072
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author Lehto, Ann
Hitscherich, Kyle
Argeros, Olga
author_facet Lehto, Ann
Hitscherich, Kyle
Argeros, Olga
author_sort Lehto, Ann
collection PubMed
description BACKGROUND: Gestational trophoblastic disease (GTD) is a rare developmental form of proliferative trophoblastic tissue. Sparse literature exists regarding the optimal management of patients with advanced GTD, but the definitive treatment is urgent surgical intervention. CASE: A 48-year-old woman presented advanced GTD. She was medically managed for hypertension and hyperthyroidism prior to surgical intervention in order to minimize the risk of anesthetic and surgical complications. CONCLUSION: Advanced GTD is rare. Undetected GTD can result in complications such as thyrotoxicosis, which poses substantial risks in the peri-operative period. Appropriate identification and management of this clinical problem are essential to prevent complications as well as subsequent malignant sequelae.
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spelling pubmed-61111262018-08-30 Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention Lehto, Ann Hitscherich, Kyle Argeros, Olga Case Rep Womens Health Article BACKGROUND: Gestational trophoblastic disease (GTD) is a rare developmental form of proliferative trophoblastic tissue. Sparse literature exists regarding the optimal management of patients with advanced GTD, but the definitive treatment is urgent surgical intervention. CASE: A 48-year-old woman presented advanced GTD. She was medically managed for hypertension and hyperthyroidism prior to surgical intervention in order to minimize the risk of anesthetic and surgical complications. CONCLUSION: Advanced GTD is rare. Undetected GTD can result in complications such as thyrotoxicosis, which poses substantial risks in the peri-operative period. Appropriate identification and management of this clinical problem are essential to prevent complications as well as subsequent malignant sequelae. Elsevier 2018-07-31 /pmc/articles/PMC6111126/ /pubmed/30167379 http://dx.doi.org/10.1016/j.crwh.2018.e00072 Text en © 2018 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lehto, Ann
Hitscherich, Kyle
Argeros, Olga
Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention
title Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention
title_full Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention
title_fullStr Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention
title_full_unstemmed Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention
title_short Advanced gestational trophoblastic disease: A case report of medical management prior to surgical intervention
title_sort advanced gestational trophoblastic disease: a case report of medical management prior to surgical intervention
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111126/
https://www.ncbi.nlm.nih.gov/pubmed/30167379
http://dx.doi.org/10.1016/j.crwh.2018.e00072
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