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Bilateral Primary Ovarian Burkitt’s Lymphoma

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dc.contributor.author Wamalwa, Emmanuel Wekesa
dc.contributor.author Chumba, David Kiprop
dc.contributor.author Kibet, Kibor Keitany
dc.contributor.author Patel, Kirtika
dc.date.accessioned 2022-01-25T06:06:11Z
dc.date.available 2022-01-25T06:06:11Z
dc.date.issued 2018
dc.identifier.uri https://link.springer.com/article/10.1007%2Fs40944-018-0178-9
dc.identifier.uri http://ir.mu.ac.ke:8080/jspui/handle/123456789/5772
dc.description.abstract We report a very rare case of primary bilateral ovarian Burkitt’s lymphoma. A 17-year-old girl was referred to Moi Teaching and Referral Hospital 2 weeks after cesarean section that was performed at a peripheral facility. A pelvic mass had been noted during cesarean section, and a biopsy of the mass had been taken. On examination, the abdomen was distended with ascites and palpable pelvic masses. Serum CA125 was elevated. Initial diagnosis was ovarian malignancy. An exploratory laparotomy was done, and bilateral ovarian masses were found, as well as ascites and omental caking. Histological findings and immunohistochemical staining confirmed Burkitt’s lymphoma. Evaluation of bone marrow aspirate and peripheral blood film yielded normal findings. Postoperatively, patient deteriorated and died 19 days following surgery, before initiation of chemotherapy. en_US
dc.language.iso en en_US
dc.publisher Springer en_US
dc.subject Ovarian Burkitt’s Lymphoma en_US
dc.title Bilateral Primary Ovarian Burkitt’s Lymphoma en_US
dc.type Article en_US


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