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Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy
Cushing syndrome resulting from adrenocortical carcinoma in pregnancy is exceedingly rare. There are no validated guidelines to establish a diagnosis or guide management in pregnancy. We provide a case of a 31-year-old woman presenting for management of diabetes in pregnancy who appeared cushingoid....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652247/ https://www.ncbi.nlm.nih.gov/pubmed/38021076 http://dx.doi.org/10.1210/jcemcr/luad118 |
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author | Morris, Jack Andrew Campbell, Peter Xu, Lily O’Sullivan, Anthony John |
author_facet | Morris, Jack Andrew Campbell, Peter Xu, Lily O’Sullivan, Anthony John |
author_sort | Morris, Jack Andrew |
collection | PubMed |
description | Cushing syndrome resulting from adrenocortical carcinoma in pregnancy is exceedingly rare. There are no validated guidelines to establish a diagnosis or guide management in pregnancy. We provide a case of a 31-year-old woman presenting for management of diabetes in pregnancy who appeared cushingoid. She was subsequently diagnosed with ACTH-independent Cushing syndrome and experienced preterm labor at 33 weeks’ gestation, delivering a healthy infant. Four weeks postpartum, the patient underwent a left adrenalectomy and was subsequently diagnosed with adrenocortical carcinoma. |
format | Online Article Text |
id | pubmed-10652247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106522472023-11-16 Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy Morris, Jack Andrew Campbell, Peter Xu, Lily O’Sullivan, Anthony John JCEM Case Rep Case Report Cushing syndrome resulting from adrenocortical carcinoma in pregnancy is exceedingly rare. There are no validated guidelines to establish a diagnosis or guide management in pregnancy. We provide a case of a 31-year-old woman presenting for management of diabetes in pregnancy who appeared cushingoid. She was subsequently diagnosed with ACTH-independent Cushing syndrome and experienced preterm labor at 33 weeks’ gestation, delivering a healthy infant. Four weeks postpartum, the patient underwent a left adrenalectomy and was subsequently diagnosed with adrenocortical carcinoma. Oxford University Press 2023-11-16 /pmc/articles/PMC10652247/ /pubmed/38021076 http://dx.doi.org/10.1210/jcemcr/luad118 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Morris, Jack Andrew Campbell, Peter Xu, Lily O’Sullivan, Anthony John Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy |
title | Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy |
title_full | Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy |
title_fullStr | Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy |
title_full_unstemmed | Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy |
title_short | Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy |
title_sort | cushing syndrome due to adrenocortical carcinoma during pregnancy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652247/ https://www.ncbi.nlm.nih.gov/pubmed/38021076 http://dx.doi.org/10.1210/jcemcr/luad118 |
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