Other Names for this Disease
- Agnogenic myeloid metaplasia
- Idiopathic myelofibrosis
- Myeloid metaplasia
- Primary myelofibrosis
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 Scarring of the bone marrow causes anemia, which can lead to fatigue and weakness, as well as pooling of the blood in abnormal sites like the liver and spleen, causing these organs to swell. Although myelofibrosis can occur at any age, it typically develops after the age of 50. In most cases, myelofibrosis gets progressively worse. Treatment is aimed at relieving signs and symptoms and may include medications, blood transfusions, chemotherapy, radiation therapy and surgery.Myelofibrosis is a disorder of the bone marrow, in which the marrow is replaced by fibrous (scar) tissue.
Last updated: 8/17/2011
- Dugdale DC, Mason JR. Primary myelofibrosis. MedlinePlus. July 11, 2008; http://www.nlm.nih.gov/medlineplus/ency/article/000531.htm. Accessed 1/7/2008.
- Myelofibrosis. MayoClinic.com. February 1, 2007; http://www.mayoclinic.com/print/myelofibrosis/DS00886/DSECTION=all&METHOD=print. Accessed 1/7/2008.
- Genetics Home Reference (GHR) contains information on Myelofibrosis. This website is maintained by the National Library of Medicine.
- MayoClinic.com offers additional information about myelofibrosis. Click on the above link to access this information.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.
- The MPN Education Foundation provides information on Myelofibrosis.
- The Leukemia & Lymphoma Society has an article on idiopathic myelofibrosis. Click on Leukemia & Lymphoma Society to view the article.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Myelofibrosis. Click on the link to view a sample search on this topic.