Burkitt Lymphoma was first described in 1958 at Mulago Hospital in Uganda. It is characterised by Burkitt cells, which have a very high proliferative rate (more than 90% Ki67 proliferative index and a 24-hour cell turnover rate), and c-MYC gene translocations.
Classification of Burkitt Lymphoma
Classification
Description
African (endemic) type
Common in equatorial Africa. It affects children and is strongly associated with EBV. It presents with tumors in the mandible, kidneys, ovaries, and adrenal medulla.
Sporadic (non-endemic) type
Occurs wordlwide. Presents with tumors in the abdomen, cecum, and peritoneum.
Immunodeficiency-associated type
Occurs in patients with HIV/AIDS and post-transplantation. Presents with nodal and extranodal disease. May resemble either the endemic or sporadic form.
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