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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.
Affiliation
  • Sheklabadi E; Prevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, No. 24, Parvaneh Street, Velenjak, P.O. Box: 19395 - 4763, Tehran, Iran.
  • Sharifi Y; Prevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, No. 24, Parvaneh Street, Velenjak, P.O. Box: 19395 - 4763, Tehran, Iran.
  • Tabarraee M; Department of Radiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Tamehrizadeh SS; Department of Hemato-Oncology, Taleghani Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Rabiee P; Prevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, No. 24, Parvaneh Street, Velenjak, P.O. Box: 19395 - 4763, Tehran, Iran.
  • Hadaegh F; Rajaie Cardiovascular, Medical and Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Thromb J ; 20(1): 39, 2022 Jul 05.
Article in En | MEDLINE | ID: mdl-35790995
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Thromb J Year: 2022 Type: Article Affiliation country: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Thromb J Year: 2022 Type: Article Affiliation country: Iran