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Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case
BACKGROUND: Bilateral adrenal hemorrhage (BAH) is a rare but potentially catastrophic condition. Its clinical manifestation is often non-specific and sometimes difficult to be diagnosed in time. CASE SUMMARY: A 57-year-old woman, who presented with severe fatigue, nausea and vomiting after left hip...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829824/ https://www.ncbi.nlm.nih.gov/pubmed/31684918 http://dx.doi.org/10.1186/s12894-019-0536-7 |
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author | Wang, Lei Wang, Xiao-fei Qin, Ying-chao Chen, Jia Shang, Cun-hai Sun, Guo-feng Li, Ning-chen |
author_facet | Wang, Lei Wang, Xiao-fei Qin, Ying-chao Chen, Jia Shang, Cun-hai Sun, Guo-feng Li, Ning-chen |
author_sort | Wang, Lei |
collection | PubMed |
description | BACKGROUND: Bilateral adrenal hemorrhage (BAH) is a rare but potentially catastrophic condition. Its clinical manifestation is often non-specific and sometimes difficult to be diagnosed in time. CASE SUMMARY: A 57-year-old woman, who presented with severe fatigue, nausea and vomiting after left hip arthroplasty due to her femoral neck fracture in a local hospital, was transferred to our medical center. Laboratory results revealed significant hyponatremia, low serum cortisol and elevated serum ACTH. Computed tomography (CT) showed a bilateral adrenal mass, measured 3.6 × 2.7 cm on the left and 3.4 × 2.3 cm on the right. Further magnetic resonance imaging (MRI) confirmed the diagnosis of BAH. The patient was prescribed with oral prednisolone acetate, 5 mg, tid, and her condition improved gradually. Nine months after, the patient was in good condition with 5 mg prednisolone acetate per day. CT revealed a clearly shrunken adrenal mass compared with 9 months ago. CONCLUSIONS: This case illustrates the difficulty in making the diagnosis of BAH with atypical presentation. Such cases necessitate greater alertness on the part of the clinician and require rapid diagnosis and prompt glucocorticoid replacement for better clinical outcomes. |
format | Online Article Text |
id | pubmed-6829824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68298242019-11-07 Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case Wang, Lei Wang, Xiao-fei Qin, Ying-chao Chen, Jia Shang, Cun-hai Sun, Guo-feng Li, Ning-chen BMC Urol Case Report BACKGROUND: Bilateral adrenal hemorrhage (BAH) is a rare but potentially catastrophic condition. Its clinical manifestation is often non-specific and sometimes difficult to be diagnosed in time. CASE SUMMARY: A 57-year-old woman, who presented with severe fatigue, nausea and vomiting after left hip arthroplasty due to her femoral neck fracture in a local hospital, was transferred to our medical center. Laboratory results revealed significant hyponatremia, low serum cortisol and elevated serum ACTH. Computed tomography (CT) showed a bilateral adrenal mass, measured 3.6 × 2.7 cm on the left and 3.4 × 2.3 cm on the right. Further magnetic resonance imaging (MRI) confirmed the diagnosis of BAH. The patient was prescribed with oral prednisolone acetate, 5 mg, tid, and her condition improved gradually. Nine months after, the patient was in good condition with 5 mg prednisolone acetate per day. CT revealed a clearly shrunken adrenal mass compared with 9 months ago. CONCLUSIONS: This case illustrates the difficulty in making the diagnosis of BAH with atypical presentation. Such cases necessitate greater alertness on the part of the clinician and require rapid diagnosis and prompt glucocorticoid replacement for better clinical outcomes. BioMed Central 2019-11-04 /pmc/articles/PMC6829824/ /pubmed/31684918 http://dx.doi.org/10.1186/s12894-019-0536-7 Text en © The Author(s). 2019 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 Wang, Lei Wang, Xiao-fei Qin, Ying-chao Chen, Jia Shang, Cun-hai Sun, Guo-feng Li, Ning-chen Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
title | Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
title_full | Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
title_fullStr | Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
title_full_unstemmed | Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
title_short | Bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
title_sort | bilateral adrenal hemorrhage after hip arthroplasty: an initially misdiagnosed case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829824/ https://www.ncbi.nlm.nih.gov/pubmed/31684918 http://dx.doi.org/10.1186/s12894-019-0536-7 |
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