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免疫功能正常患者的原发性中枢神经系统低级别淋巴瘤的放射学形态

Radiologic morphology of low-grade primary central nervous system lymphoma in immunocompetent patients.

作者信息

Jahnke Kristoph, Schilling Andreas, Heidenreich Jens, Stein Harald, Brock Mario, Thiel Eckhard, Korfel Agnieszka

机构信息

Department of Hematology, Oncology and Transfusion Medicine, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.

出版信息

AJNR Am J Neuroradiol. 2005 Nov-Dec;26(10):2446-54.

Abstract

BACKGROUND AND PURPOSE

Primary central nervous system lymphomas (PCNSLs) are usually high-grade and are rarely low-grade non-Hodgkin lymphomas (NHLs). On MR imaging, PCNSLs typically present as contrast-enhancing lesions in contact with the subarachnoid space without evidence of necrosis. We evaluated the radiologic morphology and clinical characteristics of low-grade PCNSLs, hypothesizing that they may differ from high-grade PCNSLs.

METHODS

Records were reviewed from 332 patients screened for inclusion in 3 multicenter prospective trials. MR imaging scans were obtained from all patients and were centrally reviewed by 2 consultant neuroradiologists.

RESULTS

Ten patients (3%) with low-grade PCNSLs (7 men and 3 women; median age, 59 years; age range, 19-61 years) were identified. Four patients had one lesion, 2 patients 2 lesions, and 4 patients had multiple lesions. The following radiologic features infrequently seen in high-grade PCNSLs were found in a substantial proportion of patients: location in deep structures or spine (n = 6); lack of periventricular location (n = 5); hyperintensity on T2-weighted images (n = 10); moderate or absent contrast enhancement (n = 6); and heterogeneous contrast enhancement (n = 5). In 8 patients, >2 of these features were present in at least one lesion, and, thus, the radiologic appearance was assessed atypical of high-grade PCNSLs. The atypical radiologic appearance in combination with atypical or mild symptoms resulted in a false or delayed diagnosis.

CONCLUSION

Low-grade PCNSLs may have a variable and atypical radiologic morphology compared with high-grade PCNSLs with the risk of false or delayed diagnosis.

摘要

背景与目的

原发性中枢神经系统淋巴瘤(PCNSL)通常为高级别,很少是低级别非霍奇金淋巴瘤(NHL)。在磁共振成像(MR)上,PCNSL通常表现为与蛛网膜下腔接触的强化病灶,无坏死迹象。我们评估了低级别PCNSL的放射学形态和临床特征,推测它们可能与高级别PCNSL不同。

方法

回顾了332例筛选纳入3项多中心前瞻性试验的患者记录。对所有患者进行了MR成像扫描,并由2名神经放射科顾问进行集中阅片。

结果

确定了10例(3%)低级别PCNSL患者(7例男性和3例女性;中位年龄59岁;年龄范围19 - 61岁)。4例患者有1个病灶,2例患者有2个病灶,4例患者有多个病灶。在相当比例的患者中发现了高级别PCNSL中不常见的以下放射学特征:位于深部结构或脊柱(n = 6);不在脑室周围(n = 5);T2加权像上高信号(n = 10);中度强化或无强化(n = 6);以及不均匀强化(n = 5)。在8例患者中,至少有一个病灶存在>2种这些特征,因此,放射学表现被评估为非典型的高级别PCNSL。非典型的放射学表现与非典型或轻微症状相结合导致了误诊或诊断延迟。

结论

与高级别PCNSL相比,低级别PCNSL可能具有可变的非典型放射学形态,存在误诊或诊断延迟的风险。

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