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Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review
BACKGROUND: Adrenal hemorrhage (AH) is a rare condition that can result in a life-threatening medical emergency. This medical condition could be caused by several underlying factors, one of which is the use of anticoagulants. As far as we are aware, direct oral anticoagulant (DOAC) agents are a rare...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254566/ https://www.ncbi.nlm.nih.gov/pubmed/35790995 http://dx.doi.org/10.1186/s12959-022-00397-9 |
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author | Sheklabadi, Elahe Sharifi, Yasaman Tabarraee, Mahdi Tamehrizadeh, Seyed Saeed Rabiee, Parham Hadaegh, Farzad |
author_facet | Sheklabadi, Elahe Sharifi, Yasaman Tabarraee, Mahdi Tamehrizadeh, Seyed Saeed Rabiee, Parham Hadaegh, Farzad |
author_sort | Sheklabadi, Elahe |
collection | PubMed |
description | BACKGROUND: Adrenal hemorrhage (AH) is a rare condition that can result in a life-threatening medical emergency. This medical condition could be caused by several underlying factors, one of which is the use of anticoagulants. As far as we are aware, direct oral anticoagulant (DOAC) agents are a rare but possible cause of AH. CASE PRESENTATION: Herein, we described two cases of AH due to DOACs. The first case was a 35-year-old Iranian woman with a past medical history of Hashimoto thyroiditis who was being treated with apixaban due to the previous thrombosis. Her first symptoms of AH (November 2021) were strangely similar to symptoms of autoimmune Addison disease (AAD) which led to a confirmed diagnosis of autoimmune polyendocrine syndrome type 2 (APS-2). An abdominal MRI revealed an oval shape well-encapsulated cystic mass with a diameter of 20 × 14 mm with a thick and low signal intensity rim in the left adrenal gland, highly suggestive of sub-acute left-sided AH. Our second case was an 89-year-old Iranian woman who had been admitted to the hospital (August 2021) with low blood pressure and disorientation. At the beginning of her admission, the evaluation showed hyponatremia, and further evaluations confirmed adrenal insufficiency (AI). The patient reported rivaroxaban usage for deep vein thrombosis prophylaxis after femur fixation surgery. Her abdominal CT scans showed bilateral adrenal masses highly suggestive of AH. Her follow-up examination showed persistent AI after three months. CONCLUSION: Given the history of our cases, physicians should be aware of AH in patients receiving DOACs, particularly in elderly patients who are at high risk of bleeding. It is also worth noting that AH can occur in any patient with any medical history and history of DOAC use, which is why patients must be closely monitored. |
format | Online Article Text |
id | pubmed-9254566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92545662022-07-06 Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review Sheklabadi, Elahe Sharifi, Yasaman Tabarraee, Mahdi Tamehrizadeh, Seyed Saeed Rabiee, Parham Hadaegh, Farzad Thromb J Case Report BACKGROUND: Adrenal hemorrhage (AH) is a rare condition that can result in a life-threatening medical emergency. This medical condition could be caused by several underlying factors, one of which is the use of anticoagulants. As far as we are aware, direct oral anticoagulant (DOAC) agents are a rare but possible cause of AH. CASE PRESENTATION: Herein, we described two cases of AH due to DOACs. The first case was a 35-year-old Iranian woman with a past medical history of Hashimoto thyroiditis who was being treated with apixaban due to the previous thrombosis. Her first symptoms of AH (November 2021) were strangely similar to symptoms of autoimmune Addison disease (AAD) which led to a confirmed diagnosis of autoimmune polyendocrine syndrome type 2 (APS-2). An abdominal MRI revealed an oval shape well-encapsulated cystic mass with a diameter of 20 × 14 mm with a thick and low signal intensity rim in the left adrenal gland, highly suggestive of sub-acute left-sided AH. Our second case was an 89-year-old Iranian woman who had been admitted to the hospital (August 2021) with low blood pressure and disorientation. At the beginning of her admission, the evaluation showed hyponatremia, and further evaluations confirmed adrenal insufficiency (AI). The patient reported rivaroxaban usage for deep vein thrombosis prophylaxis after femur fixation surgery. Her abdominal CT scans showed bilateral adrenal masses highly suggestive of AH. Her follow-up examination showed persistent AI after three months. CONCLUSION: Given the history of our cases, physicians should be aware of AH in patients receiving DOACs, particularly in elderly patients who are at high risk of bleeding. It is also worth noting that AH can occur in any patient with any medical history and history of DOAC use, which is why patients must be closely monitored. BioMed Central 2022-07-05 /pmc/articles/PMC9254566/ /pubmed/35790995 http://dx.doi.org/10.1186/s12959-022-00397-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Sheklabadi, Elahe Sharifi, Yasaman Tabarraee, Mahdi Tamehrizadeh, Seyed Saeed Rabiee, Parham Hadaegh, Farzad Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review |
title | Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review |
title_full | Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review |
title_fullStr | Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review |
title_full_unstemmed | Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review |
title_short | Adrenal hemorrhage following direct oral anticoagulant (DOAC) therapy: two case reports and literature review |
title_sort | adrenal hemorrhage following direct oral anticoagulant (doac) therapy: two case reports and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254566/ https://www.ncbi.nlm.nih.gov/pubmed/35790995 http://dx.doi.org/10.1186/s12959-022-00397-9 |
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