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眼眶及眼附属器淋巴瘤患者全身受累的患病率、性质及初诊时的分期

Prevalence and nature of systemic involvement and stage at initial examination in patients with orbital and ocular adnexal lymphoma.

作者信息

Hatef Elham, Roberts Dianna, McLaughlin Peter, Pro Barbara, Esmaeli Bita

机构信息

Section of Ophthalmology, Unit 441, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.

出版信息

Arch Ophthalmol. 2007 Dec;125(12):1663-7. doi: 10.1001/archopht.125.12.1663.

Abstract

OBJECTIVE

To determine the stage at initial examination and the prevalence of systemic involvement in patients with orbital and ocular adnexal lymphoma.

METHODS

The medical records of all patients with orbital and ocular adnexal lymphoma treated in a recent 7-year period were reviewed for stage at initial examination, highest stage during the follow-up period, and recurrence-free survival.

RESULTS

Forty-three patients were included. Nineteen patients had mucosa-associated lymphoid tissue, 9 had follicular, 9 had diffuse large-cell, 3 had mantle cell, 2 had small lymphocytic, and 1 had large T-cell lymphoma. The staging workup included chest radiography; orbital computed tomography or magnetic resonance imaging; computed tomography of the chest, abdomen, and pelvis; and bone marrow biopsy. Thirty-six patients had total body positron emission tomography, 7 had gallium scans, and 16 had gastrointestinal endoscopy. Lymphoma stage at diagnosis was IE in 18 patients, II in 6, and IV in 19. Six of 19 patients with mucosa-associated lymphoid tissue, 7 of 9 patients with follicular, 6 of 9 patients with diffuse large-cell, and 3 of 3 patients with mantle cell lymphoma had non-stage IE disease at initial examination. The 5-year recurrence-free survival was 64.6% for the entire cohort.

CONCLUSIONS

Extraorbital involvement is present at diagnosis in more than half of patients with orbital and ocular adnexal lymphoma and warrants extensive systemic workup at diagnosis, continued surveillance, and consideration of systemic therapy.

摘要

目的

确定眼眶及眼附属器淋巴瘤患者初诊时的分期及全身受累情况。

方法

回顾近7年治疗的所有眼眶及眼附属器淋巴瘤患者的病历,了解初诊时的分期、随访期间的最高分期及无复发生存情况。

结果

共纳入43例患者。19例为黏膜相关淋巴组织淋巴瘤,9例为滤泡性淋巴瘤,9例为弥漫大B细胞淋巴瘤,3例为套细胞淋巴瘤,2例为小淋巴细胞淋巴瘤,1例为大T细胞淋巴瘤。分期检查包括胸部X线检查、眼眶计算机断层扫描或磁共振成像、胸部、腹部及盆腔计算机断层扫描以及骨髓活检。36例患者进行了全身正电子发射断层扫描,7例进行了镓扫描,16例进行了胃肠道内镜检查。诊断时淋巴瘤分期为IE期的有18例,II期6例,IV期19例。19例黏膜相关淋巴组织淋巴瘤患者中有6例、9例滤泡性淋巴瘤患者中有7例、9例弥漫大B细胞淋巴瘤患者中有6例、3例套细胞淋巴瘤患者中有3例在初诊时为非IE期疾病。整个队列的5年无复发生存率为64.6%。

结论

超过半数的眼眶及眼附属器淋巴瘤患者在诊断时存在眶外受累,因此在诊断时需要进行全面的全身检查、持续监测并考虑全身治疗。

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