Department of Neurobiology, Harvard Medical School, Boston, MA, USA; Department of Psychology, Princeton University, Princeton, NJ, USA; Princeton Neuroscience Institute, Princeton, NJ, USA.
Department of Psychology, Durham University, Durham, UK.
Neuropsychologia. 2019 May;128:150-165. doi: 10.1016/j.neuropsychologia.2018.05.008. Epub 2018 May 9.
Patients with injury to early visual cortex or its inputs can display the Riddoch phenomenon: preserved awareness for moving but not stationary stimuli. We provide a detailed case report of a patient with the Riddoch phenomenon, MC. MC has extensive bilateral lesions to occipitotemporal cortex that include most early visual cortex and complete blindness in visual field perimetry testing with static targets. Nevertheless, she shows a remarkably robust preserved ability to perceive motion, enabling her to navigate through cluttered environments and perform actions like catching moving balls. Comparisons of MC's structural magnetic resonance imaging (MRI) data to a probabilistic atlas based on controls reveals that MC's lesions encompass the posterior, lateral, and ventral early visual cortex bilaterally (V1, V2, V3A/B, LO1/2, TO1/2, hV4 and VO1 in both hemispheres) as well as more extensive damage to right parietal (inferior parietal lobule) and left ventral occipitotemporal cortex (VO1, PHC1/2). She shows some sparing of anterior occipital cortex, which may account for her ability to see moving targets beyond ~15 degrees eccentricity during perimetry. Most strikingly, functional and structural MRI revealed robust and reliable spared functionality of the middle temporal motion complex (MT+) bilaterally. Moreover, consistent with her preserved ability to discriminate motion direction in psychophysical testing, MC also shows direction-selective adaptation in MT+. A variety of tests did not enable us to discern whether input to MT+ was driven by her spared anterior occipital cortex or subcortical inputs. Nevertheless, MC shows rich motion perception despite profoundly impaired static and form vision, combined with clear preservation of activation in MT+, thus supporting the role of MT+ in the Riddoch phenomenon.
对运动刺激有知觉,而对静止刺激无知觉。我们提供了一例里多克现象患者 MC 的详细病例报告。MC 双侧枕颞叶皮质广泛损伤,包括大部分早期视觉皮层,视野测试中静态目标完全失明。然而,她表现出令人惊讶的强大的感知运动能力,使她能够在杂乱的环境中导航,并进行捕捉运动球等动作。将 MC 的结构磁共振成像(MRI)数据与基于对照的概率图谱进行比较,发现 MC 的病变包括双侧后部、外侧和腹侧早期视觉皮层(V1、V2、V3A/B、LO1/2、TO1/2、hV4 和 VO1),以及右侧顶叶(下顶叶小叶)和左侧腹侧枕颞叶皮层(VO1、PHC1/2)的更广泛损伤。她表现出前枕叶皮层的一些保留,这可能解释了她在视野检查中能够看到 15 度以外的移动目标的能力。最引人注目的是,功能和结构 MRI 显示双侧中颞运动复合体(MT+)的功能保留强大而可靠。此外,与她在心理物理测试中辨别运动方向的能力一致,MC 也表现出 MT+中的方向选择性适应。各种测试都无法确定 MT+的输入是来自她保留的前枕叶皮层还是皮质下输入。尽管她的静态和形态视觉严重受损,但 MC 仍表现出丰富的运动知觉,同时 MT+的激活明显保留,因此支持 MT+在里多克现象中的作用。