Clinical characteristics and treatment of primary ovarian malignant lymphoma

J. Zhao, Hua-qing Wang, Ping Wang
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Abstract

Objective: To investigate the clinical features and prognostic factors of primary ovarian lymphoma(POL). Methods: A retrospective review was performed based on the clinical records of 14 POL cases treated at Tianjin Medical University Oncology institute Hospital verity from 2000-6 to 2010-5. Results: The median age of patients was 47 years at presentation(range 28~62years). Abdominal pain was the most common initial symptom. The majority of histological subtype was B cell lymphoma, above 50% of which is diffuse large B-cell non-Hodgkin's lymphoma. A R0 resection was carried out in 2 patients who were lost to follow-up soon after surgery. 11 patients were treated by CHOP, FC or CHOPE chemotherapy. Chemotherapy combined with rituximab were given to 5 patients. Until now, 5 patients were alive, 6 patients died, and only one patient was lost to follow up after therapy. Conclusion: POL is an extremely rare lymphoma. The ultimate diagnosis depends on histopathologic examination. Primary ovarian non-Hodgkin lymphoma should be treated with multi-modality strategies. Treatment with doxorubicin-based chemotherapy after oophorotomy is recommended. B cell lymphoma preferred to use rituximab combination chemotherapy. Abdominal cavity chemotherapy prophylaxis and irradiation can decrease the probability for recurrence .
原发性卵巢恶性淋巴瘤的临床特点及治疗
目的:探讨原发性卵巢淋巴瘤(POL)的临床特点及影响预后的因素。方法:回顾性分析天津医科大学肿瘤研究所附属医院2000-6 ~ 2010-5年间收治的14例POL患者的临床资料。结果:患者发病时中位年龄为47岁(28~62岁)。腹痛是最常见的首发症状。组织学亚型以B细胞淋巴瘤为主,其中弥漫性大B细胞非霍奇金淋巴瘤占50%以上。2例术后未随访的患者行R0切除。11例患者接受CHOP、FC或CHOP化疗。化疗联合利妥昔单抗5例。截至目前,存活5例,死亡6例,治疗后失访1例。结论:POL是一种极为罕见的淋巴瘤。最终的诊断取决于组织病理学检查。原发性卵巢非霍奇金淋巴瘤应采用多种治疗策略。建议在卵巢切开术后进行以阿霉素为基础的化疗。B细胞淋巴瘤首选利妥昔单抗联合化疗。腹腔化疗预防和放疗可降低复发概率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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