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Common and Uncommon Features of Central Nervous System Lymphoma on Traditional and Advanced Imaging Modalities

机译:传统和高级影像学方法对中枢神经系统淋巴瘤的共同和罕见特征

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Central nervous system (CNS) lymphoma can occur in isolation as a primary CNS neoplasm or can show systemic lymphoma involvement. Primary CNS lymphomas in patients who are immunocompetent are typically hyperattenuated on CT and iso- to hypointense relative to gray matter on T1- and T2-weighted images. On postcontrast scans, strong homogeneous enhancement is common. Most primary CNS lymphomas contact a CSF surface (either the ventricular ependyma or the pia). Advanced MR imaging may help to differentiate primary CNS lymphomas from other brain lesions. Typical primary CNS lymphomas are highly cellular tumors without necrosis; the lesions are hyperintense on diffusion-weighted images and hypointense on apparent diffusion coefficient maps. The relative cerebral blood volume ratios of primary CNS lymphomas are much lower than those of high-grade gliomas and metastases. On MR spectroscopy, elevated choline as well as a decreased N -acetylaspartate peak and high lipid peak are observed. Unlike high-grade gliomas, hemorrhages and calcifications are rare. Unusual imaging features of primary CNS lymphomas include patchy, streaky, or no enhancement; hemorrhage; necrosis; and calcifications. In patients who are immunocompromised, primary CNS lymphomas show central necrosis and peripheral enhancement. Systemic lymphomas can involve the CNS: two-thirds of patients with secondary CNS lymphoma present with leptomeningeal spread, and one-third present with parenchymal disease. An accurate diagnosis of CNS lymphoma is crucial for proper management and prognosis in both patients who are immunocompetent and those patients who are immunocompromised. The imaging features described herein may allow earlier recognition of CNS lymphoma and thus facilitate optimal treatment. Learning Objective: Recognize common and uncommon types of primary CNS lymphomas in patients who are immunocompetent and patients who are immunocompromised as well as variation in the appearance of secondary CNS lymphoma on MRI and to describe characteristic imaging findings by using advanced imaging techniques.
机译:中枢神经系统(CNS)淋巴瘤可单独作为原发性CNS肿瘤发生,或显示全身淋巴瘤受累。具有免疫功能的患者的原发性中枢神经系统淋巴瘤通常在CT上表现为高度衰减,相对于T1和T2加权图像上的灰质,其等值于低等。在对比后扫描中,通常会出现强烈的均匀增强。大多数原发性中枢神经系统淋巴瘤会接触脑脊液表面(室管膜室间隔瘤或pia)。先进的MR成像可能有助于将原发性中枢神经系统淋巴瘤与其他脑部病变区分开。典型的原发性中枢神经系统淋巴瘤是高度细胞性肿瘤,无坏死。在扩散加权图像上,病变是高强度的;在表观扩散系数图上,病变是低强度的。原发性中枢神经系统淋巴瘤的相对脑血容量比远低于高级神经胶质瘤和转移瘤。在MR光谱上,观察到胆碱升高以及N-乙酰天冬氨酸峰和高脂质峰降低。与高级神经胶质瘤不同,出血和钙化很少见。原发性中枢神经系统淋巴瘤的异常影像学特征包括斑片状,条纹状或无增强。出血;坏死和钙化。在免疫功能低下的患者中,原发性中枢神经系统淋巴瘤表现出中央坏死和周围增强。系统性淋巴瘤可累及中枢神经系统:三分之二的继发中枢神经系统淋巴瘤患者存在软脑膜扩散,三分之一的患者存在实质性疾病。 CNS淋巴瘤的准确诊断对于有免疫能力的患者和免疫功能低下的患者而言,对于正确治疗和预后至关重要。本文所述的成像特征可以允许较早地识别CNS淋巴瘤,从而促进最佳治疗。学习目标:识别具有免疫能力的患者和免疫受损的患者的常见和罕见类型的原发性中枢神经系统淋巴瘤,以及继发性中枢神经系统淋巴瘤的MRI表现,并通过使用先进的成像技术描述特征性影像学表现。

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