Chronic Idiopathic Myelofibrosis
Medical Review
Overview of Chronic Idiopathic Myelofibrosis
Chronic Idiopathic myelofibrosis is also known as primary myelofibrosis. It is a myeloproliferative neoplasm that begins when blood cells don’t develop normally. In some conditions, polycythemia vera or essential thrombocytosis can cause idiopathic myelofibrosis.
Signs and Symptoms of Chronic Idiopathic Myelofibrosis
Fatigue, Weakness, Paleness, Shortness of breath, Bruising, Weight loss, Fever, Frequent infections, Night sweats, Feeling full after eating a small amount, Discomfort or a feeling of fullness in the abdomen (if the liver and spleen are enlarged), Bone pain
Common Causes of Chronic Idiopathic Myelofibrosis
Gene mutation
Risk Factors of Chronic Idiopathic Myelofibrosis
Another blood cell disorder, Exposure to certain chemicals, Exposure to radiation, Age more than 50
Investigation Techniques for Chronic Idiopathic Myelofibrosis
Complete blood count (CBC) to measure the number and quality of white blood cells/red blood cells/platelets, Blood chemistry tests to show how well certain organs are working, Reverse transcriptase-polymerase chain reaction (RT-PCR) to see if cells in a sample of blood and bone marrow have the JAK2 mutation, Bone marrow aspiration and biopsy to confirm whether or not you have idiopathic myelofibrosis
Treatment and Prevention of Chronic Idiopathic Myelofibrosis
Supportive treatment, Symptomatic treatment, Splenectomy, Radiation therapy, Stem cell transplant
Available Chronic Idiopathic Myelofibrosis Medicines
No medicines currently available for this condition.



