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The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report

BACKGROUND: Pregnancy complicated with adrenocortical carcinoma (ACC) is a sporadic syndrome that is characterized by hypertension, uncontrolled hypokalemia, severe heart failure, premature delivery and other adverse effects. The clinical presentation of adrenocortical carcinoma is vague and nonspec...

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Autores principales: Zhang, Yuanli, Yuan, Zeng, Qiu, Chunping, Li, Shuyi, Zhang, Shiqian, Fang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975082/
https://www.ncbi.nlm.nih.gov/pubmed/31964355
http://dx.doi.org/10.1186/s12884-020-2737-1
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author Zhang, Yuanli
Yuan, Zeng
Qiu, Chunping
Li, Shuyi
Zhang, Shiqian
Fang, Yan
author_facet Zhang, Yuanli
Yuan, Zeng
Qiu, Chunping
Li, Shuyi
Zhang, Shiqian
Fang, Yan
author_sort Zhang, Yuanli
collection PubMed
description BACKGROUND: Pregnancy complicated with adrenocortical carcinoma (ACC) is a sporadic syndrome that is characterized by hypertension, uncontrolled hypokalemia, severe heart failure, premature delivery and other adverse effects. The clinical presentation of adrenocortical carcinoma is vague and nonspecific, it is challenging to identify complications of pregnancy with adrenocortical carcinoma. Here we present a case of adrenocortical carcinoma during pregnancy. We describe how to distinguish secondary hypertension from other conditions and the importance of timely detection and treatment of such patients. CASE PRESENTATION: A 22-year-old woman 30 weeks pregnant was hospitalized with uncontrolled hypertension and hypokalemia. An ultrasound examination of the right adrenal gland revealed a large mass. She underwent transabdominal adrenalectomy, and histopathology from the sample removed revealed an adrenocortical carcinoma. Five days after surgery, the patient had a premature rupture of the fetal membranes and gave birth to a newborn girl via vaginal delivery at 32 weeks of gestation. The newborn was transferred to the neonatal pediatrics ward, and the woman started receiving chemotherapy. CONCLUSIONS: Pregnancy with adrenocortical carcinoma is a rare condition. This case alerts the obstetricians that analysis of hypertension, hypokalemia, the plasma level and circadian rhythm of plasma cortisol provides a strategy to diagnose adrenocortical carcinoma during pregnancy.
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spelling pubmed-69750822020-01-28 The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report Zhang, Yuanli Yuan, Zeng Qiu, Chunping Li, Shuyi Zhang, Shiqian Fang, Yan BMC Pregnancy Childbirth Case Report BACKGROUND: Pregnancy complicated with adrenocortical carcinoma (ACC) is a sporadic syndrome that is characterized by hypertension, uncontrolled hypokalemia, severe heart failure, premature delivery and other adverse effects. The clinical presentation of adrenocortical carcinoma is vague and nonspecific, it is challenging to identify complications of pregnancy with adrenocortical carcinoma. Here we present a case of adrenocortical carcinoma during pregnancy. We describe how to distinguish secondary hypertension from other conditions and the importance of timely detection and treatment of such patients. CASE PRESENTATION: A 22-year-old woman 30 weeks pregnant was hospitalized with uncontrolled hypertension and hypokalemia. An ultrasound examination of the right adrenal gland revealed a large mass. She underwent transabdominal adrenalectomy, and histopathology from the sample removed revealed an adrenocortical carcinoma. Five days after surgery, the patient had a premature rupture of the fetal membranes and gave birth to a newborn girl via vaginal delivery at 32 weeks of gestation. The newborn was transferred to the neonatal pediatrics ward, and the woman started receiving chemotherapy. CONCLUSIONS: Pregnancy with adrenocortical carcinoma is a rare condition. This case alerts the obstetricians that analysis of hypertension, hypokalemia, the plasma level and circadian rhythm of plasma cortisol provides a strategy to diagnose adrenocortical carcinoma during pregnancy. BioMed Central 2020-01-21 /pmc/articles/PMC6975082/ /pubmed/31964355 http://dx.doi.org/10.1186/s12884-020-2737-1 Text en © The Author(s). 2020 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
Zhang, Yuanli
Yuan, Zeng
Qiu, Chunping
Li, Shuyi
Zhang, Shiqian
Fang, Yan
The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
title The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
title_full The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
title_fullStr The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
title_full_unstemmed The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
title_short The diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
title_sort diagnosis and treatment of adrenocortical carcinoma in pregnancy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975082/
https://www.ncbi.nlm.nih.gov/pubmed/31964355
http://dx.doi.org/10.1186/s12884-020-2737-1
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