Pathologic character and diagnosis of female primary genital system diffuse large B cell lymphoma

H. Cheng, X. Tang, J. Cheng, B. Zhang, Y.-L. Zhang, W.-Q. Wang, P. Teng

Department of Obstetrics and Gynecology, XuZhou Central Hospital, Xuzhou, Jiang Su Province, China. cnxzcj2002@163.com

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• Oncology

OBJECTIVE: We investigated the clinicopathological characteristics and immunophenotype of female genital system diffuse large B-cell lymphoma (DLBCL) in order to improve diagnosis and therapy efficacy.

PATIENTS AND METHODS: The clinicopathologic features of 13 cases with primary DLBCL of the female genital system were studied retrospectively. According to the immunophenotypes, 10 cases were classified as germinal center B-cell-like DLBCL and the other 3 as non-center B-cell-like DLBCL.

RESULTS: The immunohistochemistry data showed that CD20, PAX-5, and CD79a tested positive, while CD3, CD43 and CD45RO tested negative in all 13 cases. In 7 cases EMA was positive, in 9 cases CD10 was positive, in 11 cases bcl-6 was positive, and in 9 cases MUM-1 was tested positive. In one case, the Ki-67 index was less than 59%, in 3 cases Ki-67 index was between 60% to 89% and it was more than 90% in the remaining 9 cases (the median was 90%). All 13 patients underwent hysterectomy, while in 10 of them hysterectomy was followed by chemotherapy. The survival time was 3 to 20 months.

CONCLUSIONS: Primary diffuse large B-cell lymphoma of the primary female genital system is a rare and highly invasive condition that can be easily misdiagnosed. A complete diagnosis is very important because the treatment and prognosis vary in different histological types. Moreover, the immunohistochemistry is an useful diagnostic method for this type of cancer.

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