{"title":"原发性卵巢恶性淋巴瘤的临床特点及治疗","authors":"J. Zhao, Hua-qing Wang, Ping Wang","doi":"10.3969/J.ISSN.1000-8179.20131689","DOIUrl":null,"url":null,"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 .","PeriodicalId":314105,"journal":{"name":"Clinical Oncology and Cancer Research","volume":"27 4","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical characteristics and treatment of primary ovarian malignant lymphoma\",\"authors\":\"J. Zhao, Hua-qing Wang, Ping Wang\",\"doi\":\"10.3969/J.ISSN.1000-8179.20131689\",\"DOIUrl\":null,\"url\":null,\"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 .\",\"PeriodicalId\":314105,\"journal\":{\"name\":\"Clinical Oncology and Cancer Research\",\"volume\":\"27 4\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Oncology and Cancer Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3969/J.ISSN.1000-8179.20131689\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Cancer Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3969/J.ISSN.1000-8179.20131689","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Clinical characteristics and treatment of primary ovarian malignant lymphoma
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 .