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Advancements in Burkitt Lymphoma Treatment: A Comprehensive Review

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Ben Wood
Advancements in Burkitt Lymphoma Treatment: A Comprehensive Review

The lymphatic system cancer Burkitt lymphoma is characterised by fast development and arises from aberrant B cells. Lymph node enlargement is a typical symptom of Burkitt lymphoma and can occur in the spleen, liver, bone marrow, and central nervous system. High-grade non-Hodgkin lymphoma includes Burkitt lymphoma (NHL). Burkitt Lymphoma Treatment is categorised by the World Health Organization as endemic, sporadic, and immunodeficiency-associated types, which afflict persons with HIV/AIDS and children in Africa between the ages of 4 and 7.

Among children and people with impaired immune systems across the world, Burkitt lymphoma accounts for 30% of paediatric lymphomas and fewer than 1% of instances of lymphoma.


There are three main types of Burkitt lymphoma: endemic (African), sporadic, and immunodeficiency-associated. The endemic form is most common in central Africa and New Guinea.


Doctors will also need to perform a procedure called engraftment before the new stem cells begin to make enough white blood cells and neutrophils to help the body fight infection.


If the lymphoma is still in the bone marrow, doctors might offer a stem cell transplant. These transplants can be done using stem cells from the patient or with cells from another person’s bone marrow or blood. The patient is monitored closely during this time to make sure they don’t have any side effects, such as infection or bleeding. Despite the high risk of complications, stem cell transplants can be very effective for many patients with Burkitt lymphoma. 


 

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http://thrivearticles.weebly.com/article/burkitt-lymphoma-treatment-typically-involves-chemotherapy-and-targeted-therapy-for-fighting-cancer-and-controlling-its-growth


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