Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review

Antiphospholipid syndrome (APS) is an autoimmune disorder while adrenal hemorrhage could be its rare complication. Herein, we report the case of a 32-year-old unmarried woman with a history of systemic lupus erythematosus (SLE) who was hospitalized after complaints of upper abdominal pain, limb weak...

Full description

Saved in:
Bibliographic Details
Main Authors: Weiwei Jiang, Danrui Chen, Daizhi Yang, Longyi Zeng, Wen Xu, Shuo Lin
Format: Article
Language:English
Published: Wiley 2023-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2023/6686168
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850220356038557696
author Weiwei Jiang
Danrui Chen
Daizhi Yang
Longyi Zeng
Wen Xu
Shuo Lin
author_facet Weiwei Jiang
Danrui Chen
Daizhi Yang
Longyi Zeng
Wen Xu
Shuo Lin
author_sort Weiwei Jiang
collection DOAJ
description Antiphospholipid syndrome (APS) is an autoimmune disorder while adrenal hemorrhage could be its rare complication. Herein, we report the case of a 32-year-old unmarried woman with a history of systemic lupus erythematosus (SLE) who was hospitalized after complaints of upper abdominal pain, limb weakness, and loss of appetite for 2 weeks. Laboratory examination revealed hyponatremia, low plasma cortisol levels, increased adrenocorticotropic hormone levels, and a positive anticardiolipin antibody status. Furthermore, computed tomography (CT) revealed the presence of bilateral adrenal masses. Ultimately, based on dynamic changes in CT images, these masses were diagnosed as adrenal hemorrhage owing to APS. A computer-assisted literature search was conducted to identify cases of primary adrenal insufficiency associated with APS and/or SLE. The clinical features, laboratory examination, treatments, and outcomes of these cases were summarized. Our findings emphasize the importance of screening for adrenal insufficiency in patients with SLE or APS who present with abdominal complaints, asthenia, and hyponatremia. It is also recommended to test for APS all patients with adrenal hemorrhage.
format Article
id doaj-art-77ceddeeb32449a0bc58d61a26b9c357
institution OA Journals
issn 1687-8345
language English
publishDate 2023-01-01
publisher Wiley
record_format Article
series International Journal of Endocrinology
spelling doaj-art-77ceddeeb32449a0bc58d61a26b9c3572025-08-20T02:07:06ZengWileyInternational Journal of Endocrinology1687-83452023-01-01202310.1155/2023/6686168Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature ReviewWeiwei Jiang0Danrui Chen1Daizhi Yang2Longyi Zeng3Wen Xu4Shuo Lin5Department of Endocrinology & MetabolismDepartment of Endocrinology & MetabolismDepartment of Endocrinology & MetabolismDepartment of Endocrinology & MetabolismDepartment of Endocrinology & MetabolismDepartment of Endocrinology & MetabolismAntiphospholipid syndrome (APS) is an autoimmune disorder while adrenal hemorrhage could be its rare complication. Herein, we report the case of a 32-year-old unmarried woman with a history of systemic lupus erythematosus (SLE) who was hospitalized after complaints of upper abdominal pain, limb weakness, and loss of appetite for 2 weeks. Laboratory examination revealed hyponatremia, low plasma cortisol levels, increased adrenocorticotropic hormone levels, and a positive anticardiolipin antibody status. Furthermore, computed tomography (CT) revealed the presence of bilateral adrenal masses. Ultimately, based on dynamic changes in CT images, these masses were diagnosed as adrenal hemorrhage owing to APS. A computer-assisted literature search was conducted to identify cases of primary adrenal insufficiency associated with APS and/or SLE. The clinical features, laboratory examination, treatments, and outcomes of these cases were summarized. Our findings emphasize the importance of screening for adrenal insufficiency in patients with SLE or APS who present with abdominal complaints, asthenia, and hyponatremia. It is also recommended to test for APS all patients with adrenal hemorrhage.http://dx.doi.org/10.1155/2023/6686168
spellingShingle Weiwei Jiang
Danrui Chen
Daizhi Yang
Longyi Zeng
Wen Xu
Shuo Lin
Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review
International Journal of Endocrinology
title Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review
title_full Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review
title_fullStr Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review
title_full_unstemmed Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review
title_short Adrenal Hemorrhage in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report and Literature Review
title_sort adrenal hemorrhage in patients with systemic lupus erythematosus and antiphospholipid syndrome a case report and literature review
url http://dx.doi.org/10.1155/2023/6686168
work_keys_str_mv AT weiweijiang adrenalhemorrhageinpatientswithsystemiclupuserythematosusandantiphospholipidsyndromeacasereportandliteraturereview
AT danruichen adrenalhemorrhageinpatientswithsystemiclupuserythematosusandantiphospholipidsyndromeacasereportandliteraturereview
AT daizhiyang adrenalhemorrhageinpatientswithsystemiclupuserythematosusandantiphospholipidsyndromeacasereportandliteraturereview
AT longyizeng adrenalhemorrhageinpatientswithsystemiclupuserythematosusandantiphospholipidsyndromeacasereportandliteraturereview
AT wenxu adrenalhemorrhageinpatientswithsystemiclupuserythematosusandantiphospholipidsyndromeacasereportandliteraturereview
AT shuolin adrenalhemorrhageinpatientswithsystemiclupuserythematosusandantiphospholipidsyndromeacasereportandliteraturereview