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Myelofibrosis is
a rare chronic blood disorder in which abnormal bone marrow activity
leads to the formation of scar tissue, reducing the marrow’s ability to
produce healthy blood cells. It belongs to a group of conditions called
myeloproliferative neoplasms and can develop on its own or occur after another
blood disorder.
As bone marrow function
declines, the body may produce fewer red blood cells, white blood cells,
and platelets. Anaemia can cause persistent tiredness, weakness,
dizziness, and shortness of breath. Reduced platelets may increase bruising or
bleeding, while abnormal white blood cell production can affect immunity. Myelofibrosis
may also cause an enlarged spleen, resulting in abdominal discomfort, early
fullness after meals, or pain beneath the ribs. Some patients experience fever,
night sweats, weight loss, or bone and joint discomfort.
Diagnosis commonly involves blood tests, peripheral blood examination, bone marrow biopsy, and molecular or
genetic testing to identify characteristic mutations. Treatment depends on
symptoms, disease risk, age, and overall health. Management may include medicines
to control symptoms and reduce spleen enlargement, treatments for anaemia,
blood transfusions, or other supportive therapies. In selected patients, an allogeneic
stem cell transplant may offer the possibility of long-term disease
control. Regular medical monitoring helps assess progression and treatment
response.