The initial steps for diagnosing leukemia typically involve the following: 1. Medical history: The hematologist will ask the patient about any symptoms they are experiencing and gather information about their medical history, including any previous health problems or treatments. 2. Physical examination: The doctor will perform a physical exam to assess the patient's overall health. This may include checking vital signs, examining the skin for bruises or pallor, feeling for swollen lymph nodes, inspecting the mouth for signs of infection, palpating the abdomen for enlarged organs, and evaluating the skeleton for sensitivity or pain. 3. Blood tests: The doctor may order blood tests to evaluate the number and appearance of different types of blood cells. This can help identify any abnormalities that may indicate leukemia. 4. Bone marrow aspiration and biopsy: If the blood tests suggest the possibility of leukemia, the doctor may perform a bone marrow aspiration and biopsy. This involves extracting a small sample of bone marrow from the hipbone or another large bone and examining it under a microscope to look for cancer cells. 5. Additional tests: Depending on the results of the initial tests, the doctor may order additional tests, such as imaging studies (e.g., X-rays, CT scans) or genetic tests, to further evaluate the extent and characteristics of the leukemia. It's important to note that the specific diagnostic process may vary depending on the individual case and the hematologist's clinical judgment.
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Bioética, Biossegurança e Legislação em Biotecnologia
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