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eISSN: 2581-9615 || CODEN: WJARAI || Impact Factor 8.2 ||  CrossRef DOI

Research and review articles are invited for publication in April 2026 (Volume 30, Issue 1) Submit manuscript

Ovarian Burkitt lymphoma: A rare yet clinically significant entity

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  • Ovarian Burkitt lymphoma: A rare yet clinically significant entity

Z. TAZI *, M. AHARMOUCH, K. BENCHAABOUN, S. JAYI, F-Z FDILI, H. CHAARA and M.Y. MELHOUF

Department of Gynecology, II - CHU HASSAN II – FEZ, MOROCCO.
 
Case Study
World Journal of Advanced Research and Reviews, 2024, 21(03), 2482-2484
Article DOI: 10.30574/wjarr.2024.21.3.0602
DOI url: https://doi.org/10.30574/wjarr.2024.21.3.0602
 
Received on 12 January 2024; revised on 24 March 2024; accepted on 27 March 2024\
 
Primary ovarian lymphomas are rare tumors presenting as an ovarian mass that can mimic an epithelial ovarian tumor. The average age of onset is 40 years. Burkitt lymphomas, sporadic in the Western world, typically present with abdominal involvement. Biological tests and imaging guide the diagnosis. Prognosis depends on associated bone marrow and central nervous system involvement. Treatment relies on polychemotherapy. Here, we report a case of Burkitt's lymphoma in a young woman simulating advanced bilateral ovarian cancer.
 
Cancer; Ovary; Lymphoma; Prognosis; Chemotherapy
 
https://wjarr.com/sites/default/files/fulltext_pdf/WJARR-2024-0602.pdf

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Z. TAZI, M. AHARMOUCH, K. BENCHAABOUN, S. JAYI, F-Z FDILI, H. CHAARA and M.Y. MELHOUF. Ovarian Burkitt lymphoma: A rare yet clinically significant entity. World Journal of Advanced Research and Reviews, 2024, 21(3), 2482-2484. Article DOI: https://doi.org/10.30574/wjarr.2024.21.3.0602

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