{"title":"Ocular adnexal lymphoma - a retrospective study and review of the literature.","authors":"Lucka Boltezar,Danijela Strbac,Joze Pizem,Gregor Hawlina","doi":"10.2478/raon-2024-0048","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nTo review the characteristics of all Slovenian patients with ocular adnexal lymphoma (OAL) in the period of 24 years with the aim of evaluating demographic data, lymphoma location and type, disease stage, treatment modality, local control rate and survival rate.\r\n\r\nPATIENTS AND METHODS\r\nAll patients with histologically diagnosed OAL in the main tertiary centre of Slovenia, Eye Hospital, University Medical Centre Ljubljana, who were treated at Institute of Oncology Ljubljana were included in the study. Patients' data were collected from October 1995 through April 2019.\r\n\r\nRESULTS\r\nSeventy-four patients were included in the study having a median age of 68 years at diagnosis. The majority of lymphomas were of B-cell origin (98.6%). The most frequent type was the extranodal marginal zone B-cell lymphoma (MALT) (71.6%). Orbital lymphomas were diagnosed in 56 cases (75.7%) and conjunctival in 18 cases (24.3%). Ocular manifestation was the first sign of the disease in 78.4% of patients and in 67.6% of patients ocular adnexa were the only disease location. Fifty-one patients (68.9%) were treated with radiotherapy, 7 patients (9.4%) with systemic treatment, 5 patients (6.8%) with combined radiotherapy and systemic treatment and in 11 patients, biopsy and active surveillance strategy was applied (14.9%). Local control of the disease was achieved in 96.6% of treated patients. Median overall survival of the whole study group has not been reached yet. Five-year overall survival rate was 80.1% (95% CI 68.1% - 88.5%) and 5-year lymphoma specific survival rate was 87.2% (95% CI 83.2%-91.2%).\r\n\r\nCONCLUSIONS\r\nOALs comprise a group of heterogeneous diseases with variable outcomes depending predominately on the patient's age and lymphoma type, with low grade lymphomas carrying good prognosis even in elderly patients.","PeriodicalId":21034,"journal":{"name":"Radiology and Oncology","volume":"34 1","pages":"416-424"},"PeriodicalIF":2.1000,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology and Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2478/raon-2024-0048","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
BACKGROUND
To review the characteristics of all Slovenian patients with ocular adnexal lymphoma (OAL) in the period of 24 years with the aim of evaluating demographic data, lymphoma location and type, disease stage, treatment modality, local control rate and survival rate.
PATIENTS AND METHODS
All patients with histologically diagnosed OAL in the main tertiary centre of Slovenia, Eye Hospital, University Medical Centre Ljubljana, who were treated at Institute of Oncology Ljubljana were included in the study. Patients' data were collected from October 1995 through April 2019.
RESULTS
Seventy-four patients were included in the study having a median age of 68 years at diagnosis. The majority of lymphomas were of B-cell origin (98.6%). The most frequent type was the extranodal marginal zone B-cell lymphoma (MALT) (71.6%). Orbital lymphomas were diagnosed in 56 cases (75.7%) and conjunctival in 18 cases (24.3%). Ocular manifestation was the first sign of the disease in 78.4% of patients and in 67.6% of patients ocular adnexa were the only disease location. Fifty-one patients (68.9%) were treated with radiotherapy, 7 patients (9.4%) with systemic treatment, 5 patients (6.8%) with combined radiotherapy and systemic treatment and in 11 patients, biopsy and active surveillance strategy was applied (14.9%). Local control of the disease was achieved in 96.6% of treated patients. Median overall survival of the whole study group has not been reached yet. Five-year overall survival rate was 80.1% (95% CI 68.1% - 88.5%) and 5-year lymphoma specific survival rate was 87.2% (95% CI 83.2%-91.2%).
CONCLUSIONS
OALs comprise a group of heterogeneous diseases with variable outcomes depending predominately on the patient's age and lymphoma type, with low grade lymphomas carrying good prognosis even in elderly patients.
背景回顾24年间斯洛文尼亚所有眼附件淋巴瘤(OAL)患者的特征,旨在评估人口统计学数据、淋巴瘤位置和类型、疾病分期、治疗方式、局部控制率和存活率。研究共纳入74名患者,诊断时的中位年龄为68岁。大多数淋巴瘤为 B 细胞淋巴瘤(98.6%)。最常见的类型是结节外边缘区 B 细胞淋巴瘤(MALT)(71.6%)。眼眶淋巴瘤有 56 例(75.7%),结膜淋巴瘤有 18 例(24.3%)。78.4%的患者以眼部表现为首发症状,67.6%的患者以眼部附件为唯一发病部位。51名患者(68.9%)接受了放射治疗,7名患者(9.4%)接受了全身治疗,5名患者(6.8%)接受了放射治疗和全身治疗的联合治疗,11名患者(14.9%)采用了活检和积极监测策略。96.6%的患者的病情得到了局部控制。整个研究组的中位总生存期尚未达到。5年总生存率为80.1%(95% CI 68.1% - 88.5%),5年淋巴瘤特异性生存率为87.2%(95% CI 83.2% - 91.2%)。
期刊介绍:
Radiology and Oncology is a multidisciplinary journal devoted to the publishing original and high quality scientific papers and review articles, pertinent to diagnostic and interventional radiology, computerized tomography, magnetic resonance, ultrasound, nuclear medicine, radiotherapy, clinical and experimental oncology, radiobiology, medical physics and radiation protection. Therefore, the scope of the journal is to cover beside radiology the diagnostic and therapeutic aspects in oncology, which distinguishes it from other journals in the field.