Eye Pathology Institute, Department of Neuroscience and Pharmacology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
Acta Ophthalmol. 2013 Jul;91 Thesis 5:1-27. doi: 10.1111/aos.12189.
Diffuse large B-cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) constitute two distinct subtypes of non-Hodgkin lymphoma (NHL) associated with considerable morbidity and mortality. Marked diversities with regard to molecular biology and clinical features are recognized in different subsets of the two lymphomas. Because these differences could be related to the location of the lymphoma, it is of interest to investigate the clinical and histopathological features of DLBCL and MCL involving the ocular adnexal region (i.e. the orbit, eyelids, conjunctiva, lacrimal gland and lacrimal sac). Similarly, the lacrimal gland is the only glandular structure within the orbit. Because the lacrimal gland represents an important part of the immunological system, it is of interest to investigate lymphomas involving this location with regard to clinical and histological characteristics.
To characterize the clinical and histopathological features of Danish patients with DLBCL of the ocular adnexal region between 1980 and 2009 and of Danish ocular adnexal MCL patients from 1980 to 2005. Furthermore, the aim of this PhD was to review all specimens from patients with lymphoma of the lacrimal gland in Denmark between 1975 and 2009 to determine the distribution of lymphoma subtypes of the lacrimal gland and to describe the clinicopathological features of these patients.
A total of 34 patients with DLBCL and 21 with MCL of the ocular adnexal region were identified. Twenty-seven patients had lacrimal gland lymphoma, including four DLBCLs and three MCLs from studies I and II. Elderly patients predominated in all three groups, with median ages of 78, 75 and 69 years in the DLBCL, the MCL and the lacrimal gland lymphoma groups, respectively. MCL patients had a preponderance of males, whereas females prevailed among lacrimal gland lymphoma patients. The orbit was the most common site of involvement in DLBCL and MCL. Most DLBCL patients had unilateral involvement, while MCL patients had a high frequency of bilateral involvement. Similarly, localized lymphoma was relatively frequently seen in DLBCL patients in contrast to the predominance of disseminated lymphoma in the MCL group. The majority of lacrimal gland lymphomas were low grade, and the distribution of subtypes was as follows: extranodal marginal zone lymphoma, 10 (37%); follicular lymphoma, 5 (19%); DLBCL, 4 (15%); MCL, 3 (11%); chronic lymphocytic leukaemia/small lymphatic lymphoma, 2 (7%); and unclassified B-cell lymphoma, 3 (11%). The overall survival rates at 3 and 5 years for the entire study group of DLBCL were 42% and 20%, whereas 58% and 22% of MCL patients were alive 3 and 5 years after the time of diagnosis. The 5-year overall survival rate of lacrimal gland lymphoma patients was 70%. Concordant bone marrow involvement and the International Prognostic Index score were predictive factors for the overall survival in the DLBCL group in Cox regression analysis. Rituximab-containing chemotherapy was associated with an improved survival rate in MCL patients.
Diffuse large B-cell lymphoma and MCL involving the ocular adnexal region and lymphoma of the lacrimal gland are prevalent among elderly patients. The overall prognosis in DLBCL and MCL was poor, whereas the prognosis for lacrimal gland lymphoma patients was relatively good. Concordant bone marrow involvement and the International Prognostic Index score were independent predictive factors for mortality in the DLBCL group. Chemotherapy containing rituximab significantly improved survival in the MCL group.
描述丹麦眼部附属器弥漫性大 B 细胞淋巴瘤(DLBCL)患者和眼部附属器套细胞淋巴瘤(MCL)患者的临床和组织病理学特征,研究时间为 1980 年至 2009 年。此外,本博士论文的目的是回顾丹麦 1975 年至 2009 年所有泪腺淋巴瘤患者的标本,以确定泪腺淋巴瘤的淋巴瘤亚型分布,并描述这些患者的临床病理特征。
共发现 34 例眼部附属器 DLBCL 患者和 21 例眼部附属器 MCL 患者。27 例患者患有泪腺淋巴瘤,包括来自研究 I 和 II 的 4 例 DLBCL 和 3 例 MCL。所有三组患者均以老年人为主,DLBCL、MCL 和泪腺淋巴瘤组的中位年龄分别为 78、75 和 69 岁。MCL 患者中男性居多,而泪腺淋巴瘤患者中女性居多。眼眶是 DLBCL 和 MCL 最常见的受累部位。大多数 DLBCL 患者为单侧受累,而 MCL 患者则有较高的双侧受累频率。同样,DLBCL 患者中局限性淋巴瘤相对常见,而 MCL 组中弥漫性淋巴瘤占主导地位。大多数泪腺淋巴瘤为低级别,亚型分布如下:结外边缘区淋巴瘤,10 例(37%);滤泡性淋巴瘤,5 例(19%);DLBCL,4 例(15%);MCL,3 例(11%);慢性淋巴细胞白血病/小淋巴细胞淋巴瘤,2 例(7%);未分类 B 细胞淋巴瘤,3 例(11%)。整个 DLBCL 研究组的 3 年和 5 年总生存率分别为 42%和 20%,而 MCL 患者分别有 58%和 22%在诊断后 3 年和 5 年内存活。泪腺淋巴瘤患者的 5 年总生存率为 70%。Cox 回归分析显示,骨髓一致受累和国际预后指数评分是 DLBCL 组总生存率的预测因素。含利妥昔单抗的化疗可提高 MCL 患者的生存率。
眼部附属器弥漫性大 B 细胞淋巴瘤和 MCL 以及泪腺淋巴瘤在老年人中较为常见。DLBCL 和 MCL 的总体预后较差,而泪腺淋巴瘤患者的预后相对较好。骨髓一致受累和国际预后指数评分是 DLBCL 组死亡的独立预测因素。含利妥昔单抗的化疗可显著改善 MCL 组的生存率。