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Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report

BACKGROUND: Over the last 40 years, there has been a significant increase in the incidence of testicular cancer. The epidemiologic evidence to understand this phenomenon is unclear, however exogenous estrogen exposure is thought to be a driver in the development of testicular cancer. This is of part...

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Autores principales: Chandhoke, Gursimran, Shayegan, Bobby, Hotte, Sebastien J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299550/
https://www.ncbi.nlm.nih.gov/pubmed/30563561
http://dx.doi.org/10.1186/s13256-018-1894-6
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author Chandhoke, Gursimran
Shayegan, Bobby
Hotte, Sebastien J.
author_facet Chandhoke, Gursimran
Shayegan, Bobby
Hotte, Sebastien J.
author_sort Chandhoke, Gursimran
collection PubMed
description BACKGROUND: Over the last 40 years, there has been a significant increase in the incidence of testicular cancer. The epidemiologic evidence to understand this phenomenon is unclear, however exogenous estrogen exposure is thought to be a driver in the development of testicular cancer. This is of particular importance in the transgender population because utilization of exogenous estrogen therapy is an essential aspect of the transition process. CASE: We present the case of a 38-year-old Caucasian male to female transgender patient who presented with metastatic testicular cancer 15 months after initiating estrogen therapy. She presented to our emergency department with worsening back pain and fatigue. A clinical examination revealed a right-sided testicular mass. A computed tomography scan of her abdomen/pelvis identified a right groin lesion measuring 6.4 cm, a retroperitoneal mass causing right-sided hydronephrosis, an extensive deep vein thrombosis, and pathologic abdominal lymphadenopathy. Germ cell tumor markers revealed an alpha-fetoprotein of < 2.5 μg/L and a beta-human chorionic gonadotrophin of 2526 IU/L. Her lactate dehydrogenase was 5294 U/L. Medical oncology advised the discontinuation of hormonal therapy at this time. On the basis of elevation in germ cell tumor markers and the burden of disease, she was treated with four cycles of bleomycin, etoposide, and cisplatin chemotherapy. A decision to defer upfront radical inguinal orchiectomy was made due to not wanting to have an early interruption in anticoagulation. Following the completion of the chemotherapy, a 6 cm retroperitoneal mass persisted. Due to the location of the mass and surgical morbidity associated with excision, she was followed with positron emission tomography-computed tomography by Uro-oncology, with no evidence of recurrent disease 2 years since the time of diagnosis. CONCLUSIONS: While there are recognized risks associated with estrogen therapy less is known about the extent to which exogenous estrogen can serve as a driver of malignancy. With recent experimental evidence revealing a pro-growth impact of estrogen on human testicular cells, continued reporting of similar cases in the literature is imperative to see if a link between exogenous estrogen exposure and testicular cancer exists.
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spelling pubmed-62995502018-12-20 Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report Chandhoke, Gursimran Shayegan, Bobby Hotte, Sebastien J. J Med Case Rep Case Report BACKGROUND: Over the last 40 years, there has been a significant increase in the incidence of testicular cancer. The epidemiologic evidence to understand this phenomenon is unclear, however exogenous estrogen exposure is thought to be a driver in the development of testicular cancer. This is of particular importance in the transgender population because utilization of exogenous estrogen therapy is an essential aspect of the transition process. CASE: We present the case of a 38-year-old Caucasian male to female transgender patient who presented with metastatic testicular cancer 15 months after initiating estrogen therapy. She presented to our emergency department with worsening back pain and fatigue. A clinical examination revealed a right-sided testicular mass. A computed tomography scan of her abdomen/pelvis identified a right groin lesion measuring 6.4 cm, a retroperitoneal mass causing right-sided hydronephrosis, an extensive deep vein thrombosis, and pathologic abdominal lymphadenopathy. Germ cell tumor markers revealed an alpha-fetoprotein of < 2.5 μg/L and a beta-human chorionic gonadotrophin of 2526 IU/L. Her lactate dehydrogenase was 5294 U/L. Medical oncology advised the discontinuation of hormonal therapy at this time. On the basis of elevation in germ cell tumor markers and the burden of disease, she was treated with four cycles of bleomycin, etoposide, and cisplatin chemotherapy. A decision to defer upfront radical inguinal orchiectomy was made due to not wanting to have an early interruption in anticoagulation. Following the completion of the chemotherapy, a 6 cm retroperitoneal mass persisted. Due to the location of the mass and surgical morbidity associated with excision, she was followed with positron emission tomography-computed tomography by Uro-oncology, with no evidence of recurrent disease 2 years since the time of diagnosis. CONCLUSIONS: While there are recognized risks associated with estrogen therapy less is known about the extent to which exogenous estrogen can serve as a driver of malignancy. With recent experimental evidence revealing a pro-growth impact of estrogen on human testicular cells, continued reporting of similar cases in the literature is imperative to see if a link between exogenous estrogen exposure and testicular cancer exists. BioMed Central 2018-12-19 /pmc/articles/PMC6299550/ /pubmed/30563561 http://dx.doi.org/10.1186/s13256-018-1894-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Chandhoke, Gursimran
Shayegan, Bobby
Hotte, Sebastien J.
Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
title Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
title_full Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
title_fullStr Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
title_full_unstemmed Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
title_short Exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
title_sort exogenous estrogen therapy, testicular cancer, and the male to female transgender population: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299550/
https://www.ncbi.nlm.nih.gov/pubmed/30563561
http://dx.doi.org/10.1186/s13256-018-1894-6
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