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首页> 外文期刊>Indian Journal of Ophthalmology >Extranodal marginal zone B cell lymphoma of mucosa-associated lymphoid tissue type of the ocular adnexa: Retrospective single institution review of 95 patients
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Extranodal marginal zone B cell lymphoma of mucosa-associated lymphoid tissue type of the ocular adnexa: Retrospective single institution review of 95 patients

机译:眼附件的粘膜相关淋巴样组织类型的结外边缘区B细胞淋巴瘤:回顾性单机构检查95例

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Context:There are few reports on the management of extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue type (MALT), which are based on the experience of a single institution, as opposed to large multicenter randomized trials.Aim:The aim of this study was to report on the clinical experience of a single institution.Materials and Methods:A retrospective review was undertaken of records of 95 patients with MALT lymphoma of the ocular adnexa. Histologic diagnosis of MALT lymphoma was made according to established criteria, and clinical staging was carried out to determine treatment modalities. All patients were treated by external beam irradiation (30.6–45.0 Gy) after biopsy. Additional chemotherapy was performed in accordance with the clinical stage of the disease. All the patients were treated by the same hemato-oncologist and radio-oncologist.Results:Almost all patients showed complete response, except for four patients who showed partial response. In two of 95 patients, contralateral eye showed recurrence, and they were salvaged by additional radiotherapy. The 3-year overall survival and event-free survival rates were 100 and 97%, respectively, by Kaplan–Meier survival analysis. Moreover, there were no serious radiation-associated complications.Conclusions:Radiotherapy alone can be an important treatment modality for the local control and survival in patients with localized MALT lymphoma of ocular adnexa. Systemic chemotherapy should be considered in patients with advanced stage disease.
机译:背景:关于粘膜相关淋巴样组织类型(MALT)的结外边缘区B细胞淋巴瘤的管理的报道很少,这是基于单一机构的经验,而不是大型的多中心随机试验。材料与方法:回顾性回顾了95例眼附件MALT淋巴瘤患者的病历。根据既定标准进行MALT淋巴瘤的组织学诊断,并进行临床分期以确定治疗方式。所有患者在活检后均接受外照射(30.6-45.0 Gy)治疗。根据疾病的临床阶段进行了另外的化学疗法。结果:除4例部分缓解外,几乎所有患者均表现出完全缓解。 95例患者中有2例对侧眼显示复发,并通过其他放疗予以挽救。通过Kaplan–Meier生存分析,其3年总生存率和无事件生存率分别为100%和97%。结论:单纯放疗可以作为局限性眼附件MALT淋巴瘤患者局部控制和生存的重要治疗手段。晚期疾病患者应考虑全身化疗。

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