Primary Diffuse B-cell Lymphoma of Uterine Cervix: A Case Report

H. Choi, H. Kim, Jong-Sool Kim
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Abstract

Primary diffuse large B-cell lymphoma (DLBCL) of the female genital tract is a rare case. It is hard to diagnose DLBCL of the uterine cervix before surgery because it is often misdiagnosed as cervical myoma or cervical squamous cell carcinoma. Here, we report a case of cervical DLBCL misdiagnosed as a cervical myoma. A 48-year-old premenopausal woman was referred to the gynecology department due to abnormal uterine bleeding with a normal Papanicolaou smear. The initial diagnosis according to ultrasound and computed tomography was a cervical myoma. She had undergone a hysterectomy with bilateral salpingectomy. The final diagnosis was cervical DLBCL and she was referred to the department of hematology for treatment with Rituximab combined chemotherapy. After six courses of chemotherapy, complete remission was reached. At a 2-year follow-up, the patient is alive without interval change.
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宫颈原发性弥漫性b细胞淋巴瘤1例
摘要原发性弥漫大b细胞淋巴瘤(DLBCL)发生于女性生殖道是一种罕见的病例。宫颈DLBCL术前诊断困难,常被误诊为宫颈肌瘤或宫颈鳞状细胞癌。在此,我们报告一例宫颈DLBCL误诊为宫颈肌瘤。一位48岁的绝经前妇女因子宫异常出血而被转介到妇科,帕氏涂片正常。根据超声和计算机断层扫描初步诊断为宫颈肌瘤。她接受了子宫切除术和双侧输卵管切除术。最终诊断为宫颈DLBCL,转至血液科接受利妥昔单抗联合化疗。经过6个疗程的化疗后,病情完全缓解。在2年的随访中,患者存活,无间隔变化。
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