Faculty of Medical Radiation Sciences, Lusaka Apex Medical University, Lusaka, Zambia.
Department of Imaging Sciences, Neuroradiology Division, University of Rochester, Rochester, New York.
Am J Trop Med Hyg. 2018 Feb;98(2):497-504. doi: 10.4269/ajtmh.17-0309. Epub 2018 Jan 4.
The hallmark of pediatric cerebral malaria (CM) is sequestration of parasitized red blood cells in the cerebral microvasculature. Malawi-based research using 0.35 Tesla (T) magnetic resonance imaging (MRI) established that severe brain swelling is associated with fatal CM, but swelling etiology remains unclear. Autopsy and clinical studies suggest several potential etiologies, but limitations of 0.35 T MRI precluded optimal investigations into swelling pathophysiology. A 1.5 T MRI in Zambia allowed for further investigations including susceptibility-weighted imaging (SWI). SWI is an ideal sequence for identifying regions of sequestration and microhemorrhages given the ferromagnetic properties of hemozoin and blood. Using 1.5 T MRI, Zambian children with retinopathy-confirmed CM underwent imaging with SWI, T2, T1 pre- and post-gadolinium, diffusion-weighted imaging (DWI) with apparent diffusion coefficients and T2/fluid attenuated inversion recovery sequences. Sixteen children including two with moderate/severe edema were imaged; all survived. Gadolinium extravasation was not seen. DWI abnormalities spared the gray matter suggesting vasogenic edema with viable tissue rather than cytotoxic edema. SWI findings consistent with microhemorrhages and parasite sequestration co-occurred in white matter regions where DWI changes consistent with vascular congestion were seen. Imaging findings consistent with posterior reversible encephalopathy syndrome were seen in children who subsequently had a rapid clinical recovery. High field MRI indicates that vascular congestion associated with parasite sequestration, local inflammation from microhemorrhages and autoregulatory dysfunction likely contribute to brain swelling in CM. No gross radiological blood brain barrier breakdown or focal cortical DWI abnormalities were evident in these children with nonfatal CM.
小儿疟疾性脑(CM)的标志是寄生的红细胞在脑微血管中的隔离。马拉维的一项基于 0.35 特斯拉(T)磁共振成像(MRI)的研究表明,严重的脑水肿与致命性 CM 相关,但肿胀的病因仍不清楚。尸检和临床研究表明了几种潜在的病因,但 0.35 T MRI 的局限性限制了对肿胀病理生理学的最佳研究。赞比亚的 1.5 T MRI 允许进一步的研究,包括磁敏感加权成像(SWI)。SWI 是一种识别隔离和微出血区域的理想序列,因为血色素和血液具有铁磁性。使用 1.5 T MRI,赞比亚患有经视网膜病变证实的 CM 的儿童接受了 SWI、T2、T1 预对比剂和对比剂后、弥散加权成像(DWI)和表观弥散系数以及 T2/液体衰减反转恢复序列的成像。对 16 名儿童进行了成像,包括 2 名中度/重度水肿的儿童,所有儿童均存活。未见钆外渗。DWI 异常未累及灰质,提示为血管源性水肿,伴有存活组织而非细胞毒性水肿。SWI 结果与微出血和寄生虫隔离一致,而 DWI 变化一致的血管充血则发生在白质区域。与后部可逆性脑病综合征相一致的影像学表现见于随后快速临床恢复的儿童。高场 MRI 表明,与寄生虫隔离相关的血管充血、微出血引起的局部炎症和自身调节功能障碍可能导致 CM 中的脑水肿。在这些非致命性 CM 儿童中,没有明显的大体放射性血脑屏障破坏或皮质 DWI 异常。