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Bilateral adrenal hemorrhage in polycythemia vera
Shruti Bhandari1, Katrina Agito2, Esther I Krug3
1Department of Endocrinology, Sinai Hospital of Baltimore, Baltimore, MD, USA.
Bilateral adrenal hemorrhage (BAH) is a rare but serious condition in critically ill patients. Prompt diagnosis and hydrocortisone treatment are vital for hemodynamic stability and survival.
Area of Science:
- Endocrinology
- Critical Care Medicine
Background:
- Bilateral adrenal hemorrhage (BAH) is a rare complication in critically ill patients.
- It can lead to life-threatening acute adrenal insufficiency if not recognized and treated promptly.
Observation:
- A 64-year-old male with polycythemia vera presented with unresponsiveness, fever, hypotension, tachycardia, and hypoglycemia.
- Initial investigations revealed ST-elevation on ECG, elevated troponin, hemoglobin, PT, and PTT, requiring aggressive cardiorespiratory support.
Findings:
- The patient remained hypotensive despite coronary intervention. A low random cortisol level prompted suspicion of BAH.
- Stress-dose hydrocortisone administration resulted in immediate hemodynamic stabilization.
- Non-contrast abdominal CT confirmed bilateral adrenal hemorrhage.
Implications:
- This case highlights the importance of considering BAH in critically ill patients with unexplained shock and adrenal insufficiency.
- Timely diagnosis and initiation of corticosteroid therapy are crucial for improving outcomes and reducing mortality in acute adrenal insufficiency secondary to BAH.
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