Viaccoz Aurélien, Ducray François, Tholance Yannick, Barcelos Gleicy Keli, Thomas-Maisonneuve Laure, Ghesquières Hervé, Meyronet David, Quadrio Isabelle, Cartalat-Carel Stéphanie, Louis-Tisserand Guy, Jouanneau Emmanuel, Guyotat Jacques, Honnorat Jérôme, Perret-Liaudet Armand
Neuro-oncology Department, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France (A.V., F.D., L.T.-M., S.C.-C., J.H.); INSERM U1028/CNRS UMR 5292, Lyon Neuroscience Research Center, Lyon, France (A.V., F.D., Y.T., G.K.B., L.T.-M., D.M., I.Q., J.H., A.P.-L.); Université de Lyon, Université Claude-Bernard Lyon 1, Lyon, France (A.V., F.D., L.T.-M., J.H.); Neurochemistry Unit, Biochemistry Department, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France (Y.T., I.Q., A.P.-L.); Department of Anesthesiology, Pharmacology and Intensive Care, Geneva University Hospitals, Geneva, Switzerland (G.K.B.); Hematology Department, Centre Léon Bérard, Lyon, France (H.G.); Neuroradiology Department, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France (G.L.-T.); Neurosurgery Department B, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France (E.J.); Neurosurgery Department D, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France (J.G.).
Neuro Oncol. 2015 Nov;17(11):1497-503. doi: 10.1093/neuonc/nov092. Epub 2015 May 25.
The diagnosis of primary central nervous system lymphoma (PCNSL) can be challenging. PCNSL lesions are frequently located deep within the brain, and performing a cerebral biopsy is not always feasible. The aim of this study was to investigate the diagnostic value of CSF neopterin, a marker of neuroinflammation, in immunocompetent patients with suspected PCNSL.
We retrospectively reviewed the characteristics of 124 patients with brain tumor (n = 82) or an inflammatory CNS disorder (n = 42) in whom CSF neopterin levels were assessed. Twenty-eight patients had PCNSL, 54 patients had another type of brain tumor (glioma n = 36, metastasis n = 13, other n = 5), and 13 patients had a pseudotumoral inflammatory brain lesion.
CSF neopterin levels were significantly higher in the patients with PCNSL than in those with other brain tumors (41.8 vs 5.1 nmol/L, P < .001), those with pseudotumoral inflammatory brain lesions (41.8 vs 4.3 nmol/L, P < .001), and those with nontumefactive inflammatory CNS disorders (41.8 vs 3.8 nmol/L, P < .001). In the 95 patients with space-occupying brain lesions, at a cutoff of 10 nmol/L, the sensitivity of this approach was 96% and the specificity was 93% for the diagnosis of PCNSL. The positive and negative predictive values were 84% and 98%, respectively.
Assessing CSF neopterin levels in patients with a suspected brain tumor might be helpful for the positive and differential diagnosis of PCNSL. A prospective study is warranted to confirm these results.
原发性中枢神经系统淋巴瘤(PCNSL)的诊断具有挑战性。PCNSL病变常位于脑深部,进行脑活检并非总是可行。本研究的目的是探讨神经炎症标志物脑脊液新蝶呤在免疫功能正常的疑似PCNSL患者中的诊断价值。
我们回顾性分析了124例评估了脑脊液新蝶呤水平的脑肿瘤患者(n = 82)或炎症性中枢神经系统疾病患者(n = 42)的特征。28例患者患有PCNSL,54例患者患有其他类型的脑肿瘤(胶质瘤n = 36,转移瘤n = 13,其他n = 5),13例患者患有假瘤性炎症性脑病变。
PCNSL患者的脑脊液新蝶呤水平显著高于其他脑肿瘤患者(41.8对5.1 nmol/L,P <.001)、假瘤性炎症性脑病变患者(41.8对4.3 nmol/L,P <.001)和非肿瘤性炎症性中枢神经系统疾病患者(41.8对3.8 nmol/L,P <.001)。在95例有占位性脑病变的患者中,以10 nmol/L为临界值,该方法诊断PCNSL的敏感性为96%,特异性为93%。阳性和阴性预测值分别为84%和98%。
评估疑似脑肿瘤患者的脑脊液新蝶呤水平可能有助于PCNSL的阳性诊断和鉴别诊断。有必要进行前瞻性研究以证实这些结果。