Ovarian non-Hodgkin lymphoma with central nervous system involvement: A case report

Brenda Nyamu, Eunice Cheserem
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 Case presentation: A 38-year-old presented to the gynecological oncology clinic with abdominal pain and distension. Her tumor marker CA-125 levels were elevated. She developed right-sided facial nerve palsy and blindness. A diagnosis of aggressive NHL with a differential of DLBCL was made by histopathological and immunohistochemical examination of the excised ovarian tissue. A head computed tomography scan revealed subtle enhancing opacity suspicious of lymphomatous deposits. She was lost to follow-up after ten months of chemotherapy and cranial radiotherapy.
 Conclusion: Primary lymphoma of the ovary is rare, and the prognosis is often poorer when compounded with CNS involvement. Because of poor prognosis in the presence of CNS involvement, this case highlights the need for timely diagnosis and management.","PeriodicalId":85009,"journal":{"name":"Journal of obstetrics & gynaecology of Eastern and Central Africa","volume":"142 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of obstetrics & gynaecology of Eastern and Central Africa","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59692/jogeca.v35i2.50","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background: Ovarian lymphoma is rare. Extranodal non-Hodgkin lymphoma (NHL) represents 0.5% of malignant genital diseases. Due to its rarity, there are no accepted treatment protocols. Diffuse large B cell lymphoma (DLBCL) has a central nervous system (CNS) involvement rate of 3-5%. Case presentation: A 38-year-old presented to the gynecological oncology clinic with abdominal pain and distension. Her tumor marker CA-125 levels were elevated. She developed right-sided facial nerve palsy and blindness. A diagnosis of aggressive NHL with a differential of DLBCL was made by histopathological and immunohistochemical examination of the excised ovarian tissue. A head computed tomography scan revealed subtle enhancing opacity suspicious of lymphomatous deposits. She was lost to follow-up after ten months of chemotherapy and cranial radiotherapy. Conclusion: Primary lymphoma of the ovary is rare, and the prognosis is often poorer when compounded with CNS involvement. Because of poor prognosis in the presence of CNS involvement, this case highlights the need for timely diagnosis and management.
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卵巢非霍奇金淋巴瘤累及中枢神经系统1例
背景:卵巢淋巴瘤是罕见的。结外非霍奇金淋巴瘤(NHL)占恶性生殖器疾病的0.5%。由于其罕见,没有公认的治疗方案。弥漫大B细胞淋巴瘤(DLBCL)累及中枢神经系统(CNS)的比例为3-5%。 病例介绍:一位38岁的女性因腹痛和腹胀来到妇科肿瘤诊所。肿瘤标志物CA-125水平升高。她患上了右侧面神经麻痹和失明。通过对切除卵巢组织的组织病理学和免疫组织化学检查,诊断为侵袭性NHL与DLBCL的鉴别。头部电脑断层扫描显示轻微强化混浊,怀疑有淋巴瘤沉积。化疗和颅脑放疗10个月后,患者失去随访。 结论:原发性卵巢淋巴瘤较为少见,合并中枢神经系统病变预后较差。由于中枢神经系统受累的预后较差,本病例强调及时诊断和治疗的必要性。
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