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The document discusses a clinical case of a 19-year-old male with sickle beta thalassemia who presented with respiratory distress and was diagnosed with acute pulmonary thromboembolism and aspiration pneumonitis. It outlines the pathophysiology, types of sickle cell crises, and their management, including treatments for vaso-occlusive crises and acute pulmonary embolism. Additionally, it highlights new treatments such as bone marrow and stem cell transplants, along with the role of oral anticoagulants in ma

Author

Bhu

Language

EN