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眼部附属器淋巴瘤是否需要进行中枢神经系统预防?

Is central nervous system prophylaxis necessary in ocular adnexal lymphoma?

作者信息

Restrepo A, Raez L E, Byrne G E, Johnson T, Ossi P, Benedetto P, Hamilton K, Whitcomb C C, Cassileth P A

机构信息

Department of Medicine, University of Miami School of Medicine, FL, USA.

出版信息

Crit Rev Oncog. 1998;9(3-4):269-73.

Abstract

PURPOSE

To examine the frequency of metastasis to the eye and central nervous system (CNS) from ocular adnexal lymphomas and to evaluate whether CNS prophylaxis is appropriate for these tumors.

PATIENTS AND METHODS

Seventy-one patients with biopsy-confirmed ocular adnexal lymphomas were evaluated between 1989 and 1995. The lymphomas were subclassified histopathologically according to the new Revised European-American Lymphoma (REAL) criteria. Molecular genetic analysis of tumor cell DNA was done by Southern blot. Patients had a complete ophthalmologic evaluation and metastatic work-up and were then routinely followed up by an ophthalmologist and a medical oncologist.

RESULTS

The 34 men and 37 women studied had a median age of 67 years (23 to 92). Ocular adnexal lymphomas were situated in the orbit in 54 patients, in the conjunctiva in 14 patients, and in the eyelid in 3 patients. Bilateral involvement occurred in 11 patients. The most common histologic diagnoses were (54 patients, 76%) extra-nodal marginal zone lymphomas and small lymphocytic lymphomas in 10 patients (14%). Molecular genetic analysis performed in all patients confirmed a monoclonal B-cell population in 55 patients (77%), including a single rearrangement of the immunoglobulin heavy chain gene in 14 patients, and more than two rearrangements in 41 patients. No patients had isolated T-cell gene rearrangements. Localized ocular adnexal lymphoma was diagnosed in 43 patients (61%), 17 patients (24%) were found to have concurrent extraocular lymphoma on metastatic work-up and 11 patients (15%) had a previous diagnosis of systemic lymphoma before the onset of their ocular tumor. The median duration of follow-up was 20 months. Overall, 32 patients (45%) had tumors, which remained localized to the orbit adnexa. Eleven patients (15%) relapsed, but none had eye or central nervous system involvement nor required CNS-directed therapy. Although eight patients died, only two died as a direct result of systemic lymphoma. No patient received CNS prophylaxis with either intrathecal chemotherapy and/or radiation therapy.

CONCLUSION

Ocular adnexal lymphomas are rare non-Hodgkin's B-cell lymphomas. Metastatic involvement of the eye or central nervous system is rare and CNS prophylaxis with radiotherapy or chemotherapy is unnecessary.

摘要

目的

研究眼附属器淋巴瘤转移至眼和中枢神经系统(CNS)的频率,并评估对这些肿瘤进行CNS预防性治疗是否合适。

患者与方法

对1989年至1995年间71例经活检确诊的眼附属器淋巴瘤患者进行评估。根据新的修订欧美淋巴瘤(REAL)标准对淋巴瘤进行组织病理学亚分类。通过Southern印迹法对肿瘤细胞DNA进行分子遗传学分析。患者接受了全面的眼科评估和转移灶检查,随后由眼科医生和肿瘤内科医生进行常规随访。

结果

研究的34名男性和37名女性的中位年龄为67岁(23至92岁)。眼附属器淋巴瘤位于眼眶的有54例,位于结膜的有14例,位于眼睑的有3例。11例患者为双侧受累。最常见的组织学诊断为结外边缘区淋巴瘤54例(76%),小淋巴细胞淋巴瘤10例(14%)。对所有患者进行的分子遗传学分析证实55例患者(77%)存在单克隆B细胞群体,其中14例患者免疫球蛋白重链基因有单一重排,41例患者有两个以上重排。无患者有孤立的T细胞基因重排。43例患者(61%)诊断为局限性眼附属器淋巴瘤,17例患者(24%)在转移灶检查时发现合并眼外淋巴瘤,11例患者(15%)在眼部肿瘤发病前曾诊断为系统性淋巴瘤。中位随访时间为20个月。总体而言,32例患者(45%)的肿瘤局限于眼眶附件。11例患者(15%)复发,但均无眼部或中枢神经系统受累,也无需进行CNS导向治疗。虽然8例患者死亡,但仅2例直接死于系统性淋巴瘤。无患者接受鞘内化疗和/或放射治疗进行CNS预防性治疗。

结论

眼附属器淋巴瘤是罕见的非霍奇金B细胞淋巴瘤。眼或中枢神经系统转移受累罕见,放疗或化疗进行CNS预防性治疗无必要。

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