Starkey Jay, Kobayashi Nobuo, Numaguchi Yuji, Moritani Toshio
From the Department of Radiology, St Luke's International Hospital, 9-1 Akashicho, Chuo, Tokyo 104-8560, Japan (J.S., N.K., Y.N.); and the Department of Radiology, University of Iowa Hospitals and Clinics, Iowa City, Iowa (T.M.).
Radiographics. 2017 Mar-Apr;37(2):562-576. doi: 10.1148/rg.2017160085. Epub 2017 Feb 6.
Cytotoxic lesions of the corpus callosum (CLOCCs) are secondary lesions associated with various entities. CLOCCs have been found in association with drug therapy, malignancy, infection, subarachnoid hemorrhage, metabolic disorders, trauma, and other entities. In all of these conditions, cell-cytokine interactions lead to markedly increased levels of cytokines and extracellular glutamate. Ultimately, this cascade can lead to dysfunction of the callosal neurons and microglia. Cytotoxic edema develops as water becomes trapped in these cells. On diffusion-weighted magnetic resonance (MR) images, CLOCCs manifest as areas of low diffusion. CLOCCs lack enhancement on contrast material-enhanced images, tend to be midline, and are relatively symmetric. The involvement of the corpus callosum typically shows one of three patterns: (a) a small round or oval lesion located in the center of the splenium, (b) a lesion centered in the splenium but extending through the callosal fibers laterally into the adjacent white matter, or (c) a lesion centered posteriorly but extending into the anterior corpus callosum. CLOCCs are frequently but not invariably reversible. Their pathologic mechanisms are discussed, the typical MR imaging findings are described, and typical cases of CLOCCs are presented. Although CLOCCs are nonspecific with regard to the underlying cause, additional imaging findings and the clinical findings can aid in making a specific diagnosis. Radiologists should be familiar with the imaging appearance of CLOCCs to avoid a misdiagnosis of ischemia. When CLOCCs are found, the underlying cause of the lesion should be sought and addressed. RSNA, 2017 An earlier incorrect version of this article appeared online. This article was corrected on February 13, 2017.
胼胝体细胞毒性病变(CLOCCs)是与多种疾病相关的继发性病变。已发现CLOCCs与药物治疗、恶性肿瘤、感染、蛛网膜下腔出血、代谢紊乱、创伤及其他疾病有关。在所有这些情况下,细胞因子相互作用导致细胞因子和细胞外谷氨酸水平显著升高。最终,这一连串反应可导致胼胝体神经元和小胶质细胞功能障碍。当水被困在这些细胞中时,就会形成细胞毒性水肿。在扩散加权磁共振(MR)图像上,CLOCCs表现为低扩散区域。CLOCCs在对比剂增强图像上无强化,倾向于位于中线,且相对对称。胼胝体受累通常表现为以下三种模式之一:(a)位于压部中心的小圆形或椭圆形病变;(b)以压部为中心但通过胼胝体纤维横向延伸至相邻白质的病变;或(c)以胼胝体后部为中心但延伸至胼胝体前部的病变。CLOCCs通常但并非总是可逆的。本文讨论了其病理机制,描述了典型的MR成像表现,并展示了CLOCCs的典型病例。尽管CLOCCs对于潜在病因不具有特异性,但其他影像学表现和临床发现有助于做出明确诊断。放射科医生应熟悉CLOCCs的影像学表现,以避免误诊为缺血。发现CLOCCs时,应寻找并处理病变的潜在病因。RSNA,2017 本文的一个早期错误版本已在线发表。本文于2017年2月13日进行了更正。