Koubska Eva, Weichet Jiri, Malikova Hana
Department of Radiology, Na Homolce Hospital, Prague, Czech Republic.
Neuro Endocrinol Lett. 2016 Sep;37(4):318-324.
The aim of the present study was to evaluate morphological MRI findings in histologically-proven central nervous system lymphoma (CNSL) at time of their first appearance, and to describe dynamic changes on repeat MRI before the diagnosis was histologically proven.
We retrospectively evaluated the MRI examinations of 74 patients with histologically-proven CNSL (10 secondary CNSL, 64 primary PCNSL; 10 immunocompromised, 54 immunocompetent). In 43 patients, we evaluated the evolution of CNSL on MRI before the diagnosis was proven.
Primary CNSL was typically localized supratentorially (63%), with multiple (59%) or infiltrative (36%) lesions showing diffusion restriction (98%), often (87%) reaching the brain surface. In approximately 50% of patients, meningeal, ependymal or cranial nerve involvement was found. We detected significant differences in enhancement patterns between immunocompromised and immunocompetent patients; non-homogenous enhancement present in 50% of immunocompromised patients. We did not find any significant differences in MRI appearance between primary and secondary CNSL. Regression was evident after corticosteroid treatment in 52% of patients; however, in 16% of cases overall progression was observed.
CNSL generally presents as an infiltrative lesion or multiple homogenously-enhancing lesions of the brain in contact with the brain surface. Involvement of the corpus callosum, cranial nerves, ependyma or meninges is common. No significant differences between primary and secondary CNSL were detected, however differences in enhancement type between immunocompromised and immunocompetent primary CNSL patients were found. We stress the variability of MRI findings in the course of the disease and also the variable response to corticotherapy.
本研究旨在评估经组织学证实的中枢神经系统淋巴瘤(CNSL)首次出现时的MRI形态学表现,并描述在组织学确诊之前重复MRI检查时的动态变化。
我们回顾性评估了74例经组织学证实的CNSL患者的MRI检查结果(10例继发性CNSL,64例原发性PCNSL;10例免疫功能低下,54例免疫功能正常)。在43例患者中,我们在确诊之前评估了CNSL在MRI上的演变情况。
原发性CNSL通常位于幕上(63%),多灶性(59%)或浸润性(36%)病变表现为弥散受限(98%),常累及脑表面(87%)。约50%的患者发现有脑膜、室管膜或脑神经受累。我们检测到免疫功能低下和免疫功能正常患者之间的强化模式存在显著差异;50%的免疫功能低下患者表现为不均匀强化。原发性和继发性CNSL在MRI表现上未发现任何显著差异。52%的患者在接受皮质类固醇治疗后病情明显好转;然而,16%的病例出现了总体病情进展。
CNSL通常表现为与脑表面接触的浸润性病变或多个均匀强化的脑内病变。胼胝体、脑神经、室管膜或脑膜受累很常见。未检测到原发性和继发性CNSL之间的显著差异,但发现免疫功能低下和免疫功能正常的原发性CNSL患者在强化类型上存在差异。我们强调了疾病过程中MRI表现的变异性以及对皮质激素治疗反应的变异性。