Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review

ABSTRACT Purpose To present a case series of Cushing's syndrome (CS) during pregnancy caused by adrenocortical adenomas, highlighting clinical features, hormonal assessments and outcomes. Methods We describe five pregnant women with CS, detailing clinical presentations and laboratory findings....

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Main Authors: Yan Wang, Yufen An, Xiaomei Hou, Yanan Xu, Zhen Li, Xin Liu, Fumin Zheng, Mingze Sun, Rendong Han, Caixia Lu, Jing Li, Jun Zhou
Format: Article
Language:English
Published: Wiley 2024-03-01
Series:Endocrinology, Diabetes & Metabolism
Subjects:
Online Access:https://doi.org/10.1002/edm2.474
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author Yan Wang
Yufen An
Xiaomei Hou
Yanan Xu
Zhen Li
Xin Liu
Fumin Zheng
Mingze Sun
Rendong Han
Caixia Lu
Jing Li
Jun Zhou
author_facet Yan Wang
Yufen An
Xiaomei Hou
Yanan Xu
Zhen Li
Xin Liu
Fumin Zheng
Mingze Sun
Rendong Han
Caixia Lu
Jing Li
Jun Zhou
author_sort Yan Wang
collection DOAJ
description ABSTRACT Purpose To present a case series of Cushing's syndrome (CS) during pregnancy caused by adrenocortical adenomas, highlighting clinical features, hormonal assessments and outcomes. Methods We describe five pregnant women with CS, detailing clinical presentations and laboratory findings. Results Common clinical features included a full moon face, buffalo back and severe hypertension. Elevated blood cortisol levels with circadian rhythm disruption and suppressed adrenocorticotrophic hormone (ACTH) levels were observed. Imaging revealed unilateral adrenal tumours. Two cases underwent laparoscopic adrenalectomies during the second trimester, while three had postpartum surgery. All required hormone replacement therapy, with postoperative pathological confirmation of adrenocortical adenomas. Conclusion Diagnosis of CS during pregnancy is challenging due to overlapping features with normal pregnancy: elevated blood cortisol levels and abnormal diurnal rhythm of blood cortisol, suppressed aid diagnosis. Treatment should be individualised due to a lack of explicit optimum therapeutic approaches. Laparoscopic adrenalectomy may be an optimal choice, along with multidisciplinary management including hormone replacement therapy.
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spelling doaj.art-90a1d782d2d14e78b1017fa30deda3a02024-03-25T06:14:31ZengWileyEndocrinology, Diabetes & Metabolism2398-92382024-03-0172n/an/a10.1002/edm2.474Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and ReviewYan Wang0Yufen An1Xiaomei Hou2Yanan Xu3Zhen Li4Xin Liu5Fumin Zheng6Mingze Sun7Rendong Han8Caixia Lu9Jing Li10Jun Zhou11Department of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Pathology The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaDepartment of Obstetrics The Affiliated Hospital of Qingdao University Qingdao ChinaABSTRACT Purpose To present a case series of Cushing's syndrome (CS) during pregnancy caused by adrenocortical adenomas, highlighting clinical features, hormonal assessments and outcomes. Methods We describe five pregnant women with CS, detailing clinical presentations and laboratory findings. Results Common clinical features included a full moon face, buffalo back and severe hypertension. Elevated blood cortisol levels with circadian rhythm disruption and suppressed adrenocorticotrophic hormone (ACTH) levels were observed. Imaging revealed unilateral adrenal tumours. Two cases underwent laparoscopic adrenalectomies during the second trimester, while three had postpartum surgery. All required hormone replacement therapy, with postoperative pathological confirmation of adrenocortical adenomas. Conclusion Diagnosis of CS during pregnancy is challenging due to overlapping features with normal pregnancy: elevated blood cortisol levels and abnormal diurnal rhythm of blood cortisol, suppressed aid diagnosis. Treatment should be individualised due to a lack of explicit optimum therapeutic approaches. Laparoscopic adrenalectomy may be an optimal choice, along with multidisciplinary management including hormone replacement therapy.https://doi.org/10.1002/edm2.474adrenocortical adenomaCushing's syndromepregnancy
spellingShingle Yan Wang
Yufen An
Xiaomei Hou
Yanan Xu
Zhen Li
Xin Liu
Fumin Zheng
Mingze Sun
Rendong Han
Caixia Lu
Jing Li
Jun Zhou
Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review
Endocrinology, Diabetes & Metabolism
adrenocortical adenoma
Cushing's syndrome
pregnancy
title Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review
title_full Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review
title_fullStr Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review
title_full_unstemmed Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review
title_short Cushing's Syndrome in Pregnancy Secondary to Adrenocortical Adenoma: A Case Series and Review
title_sort cushing s syndrome in pregnancy secondary to adrenocortical adenoma a case series and review
topic adrenocortical adenoma
Cushing's syndrome
pregnancy
url https://doi.org/10.1002/edm2.474
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