CML, or chronic myeloid leukemia, is a type of cancer that affects the blood and bone marrow. It is caused by a genetic mutation in the cells of the bone marrow, which leads to the production of too many white blood cells. Diagnosis of CML is important for the successful treatment of the condition.
Physical Exam
Upon diagnosis for CML, the doctor will likely start with a physical exam. During this physical exam, the doctor will evaluate the patient’s overall health and will look for any signs of CML. This may include checking for swollen lymph nodes, swelling in the spleen or liver, and any other signs that may indicate the presence of CML.
Blood Tests
Blood tests are the most common way to diagnose CML. The doctor will take a sample of the patient’s blood and analyze it for abnormalities. This may include testing for an elevated white blood cell count, which is one of the most common signs of CML. Additionally, the doctor may look for the presence of a specific genetic mutation in the cells of the bone marrow that is associated with CML.
Bone Marrow Test
In some cases, the doctor may order a bone marrow test in order to confirm a diagnosis of CML. During this test, a small sample of bone marrow will be taken from the patient and analyzed in the laboratory. The doctor will be looking for the presence of the genetic mutation associated with CML, as well as any other signs of the condition.
Imaging Tests
Imaging tests may also be ordered in order to determine the extent of the disease and to look for any signs of the spread of CML. This may include a chest x-ray, CT scan, or other types of imaging tests.
Once CML has been diagnosed, the doctor will create a treatment plan for the patient. This plan may include medications, lifestyle changes, and other treatments. It is important that the patient work with their doctor to ensure that they are receiving the best possible care for their condition.