2014, Number 2
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Cir Cir 2014; 82 (2)
Bilateral ovarian Burkitt’s lymphoma. A case presentation
Briseño-Hernández AA, Quezada-López DR, Castañeda-Chávez A, Macías-Amezcua MD, Pintor-Belmontes JC
Language: Spanish
References: 24
Page: 212-218
PDF size: 382.17 Kb.
ABSTRACT
Background: Burkitt lymphoma, is described as an aggressive form of
non-Hodgkin lymphoma of B cells which occurs most often in children
and young adults, ovarian lymphoma can appear as a primary lesion or
more commonly referred to as a metastasis. Primary ovarian lesions are
rare manifestations corresponding to 0.5% of non-Hodgkin lymphoma
and 1.5% of ovarian tumors.
Clinic case: 31 years old female with general weakness, march incapacity,
dyspnea, hyporexia, fever, diaphoresis, weight loss of 20 kg, flat abs with
abdominal pain; Ca125 610 U/ml. Abdominal computed tomography
shows a solid aspect tumor which affects the right pelvic cavity.
Bilateral ovarian tumors were removed. Microscopically, both lesions
show a “starry sky” pattern composed by a monotonous infiltration of
lymphocytes mixed with large and clear macrophages, several atypical
mitoses, and necrosis and hemorrhage areas. Immunohistochemistry
was positive for CD10, CD20, and negative for CD3 and high Ki67
proliferation index. Bilateral ovarian Burkitt’s lymphoma was diagnosed.
Conclusion: Bilateral ovarian Burkitt´s lymphoma is a rare entity, with a
variability of presentations, the abdominal pain and abdominal tumors
are the most frequent. The patient’s prognosis at short term is poor,
therefore it’s necessary to know this entity and make an early diagnosis.
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