Abstract
Adrenal hematopoiesis is a rare condition. It must be suspected in case of any incidentaloma in a patient treated for chronic hemolytic pathology. Surgery remains the most effective treatment for large symptomatic masses. We report a case of large adrenal mass in young patient with history of beta-Thalassemia intermedia, managed by open resection. The post-operative course was uneventful.
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