Schmahmann Jeremy D
Ataxia Unit, Cognitive Behavioral Neurology Unit, Laboratory for Neuroanatomy and Cerebellar Neurobiology, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, 100 Cambridge Street, Suite 2000, Boston, MA, 02114, USA.
Childs Nerv Syst. 2020 Jun;36(6):1205-1214. doi: 10.1007/s00381-019-04253-6. Epub 2019 Jun 25.
Cerebellar mutism (CM), pseudobulbar palsy, posterior fossa syndrome (PFS), and cerebellar cognitive affective syndrome (CCAS) are terms that have been used, sometimes interchangeably, to refer to the complex neurological constellation that occurs following surgical removal of cerebellar and fourth ventricular tumors, mostly in children, but also sometimes in adults.
This paper reviews the origins of what is now regarded as pediatric post-operative cerebellar mutism, the cerebellar cognitive affective syndrome, and the neurological manifestations of injury to or disruption of brainstem and cerebellar structures. It examines the specific components of each of these phenomena in the context of the evolving understanding of the role of the cerebellum in nervous system function.
Children undergoing surgical management of tumors in the posterior cranial fossa are at risk of experiencing cranial neuropathies, corticospinal damage, cerebellar ataxia and related motor disorders, neuropsychiatric and cognitive changes, and in some patients, mutism. These clinical presentations are differentiated from each other and examined in the context of the relevant anatomical structures and distributed neural circuits. The term posterior fossa syndrome is not sufficiently helpful in distinguishing the different elements of the clinical phenomena from each other, and because of this lack of precision and specificity, there is consensus among investigators in the international Posterior Fossa Society that the designation be retired.
Using contemporary brain imaging methods and guided by careful clinical observation and meticulous definition of clinical phenomenology, it is now feasible to perform detailed structure function correlation analyses to achieve two critical goals in the care of children with tumors in the posterior cranial fossa. The first goal is to identify and understand the neural circuits responsible for the different manifestations-arousal, cranial neuropathies, long tract signs, cerebellar motor syndrome, cerebellar vestibular syndrome, cerebellar cognitive affective syndrome including emotional dyscontrol, and mutism. The second goal is to transform this knowledge into practical clinical intervention, preventing the complications inherent in the necessary surgery whenever possible, and develop new approaches to treatment with methods including brain modulation targeting interconnected nodes of the damaged neural circuits.
小脑缄默症(CM)、假性球麻痹、后颅窝综合征(PFS)和小脑认知情感综合征(CCAS)这些术语有时可互换使用,用于指代小脑和第四脑室肿瘤手术切除后出现的复杂神经症候群,多见于儿童,但成人也时有发生。
本文回顾了如今被视为小儿术后小脑缄默症、小脑认知情感综合征以及脑干和小脑结构损伤或破坏的神经学表现的起源。在对小脑在神经系统功能中作用的认识不断演变的背景下,研究了这些现象各自的具体组成部分。
接受后颅窝肿瘤手术治疗的儿童有发生颅神经病变、皮质脊髓损伤、小脑共济失调及相关运动障碍、神经精神和认知改变的风险,部分患者还会出现缄默症。这些临床表现相互有别,并结合相关解剖结构和分布的神经回路进行了研究。后颅窝综合征这一术语在区分临床现象的不同要素方面帮助不大,由于缺乏精确性和特异性,国际后颅窝协会的研究人员一致认为应摒弃这一称谓。
利用当代脑成像方法,并在仔细的临床观察和对临床现象学的精确界定的指导下,现在有可能进行详细的结构功能相关性分析,以实现后颅窝肿瘤患儿护理中的两个关键目标。第一个目标是识别并理解负责不同表现——觉醒、颅神经病变、长束征、小脑运动综合征、小脑前庭综合征、包括情绪失控在内的小脑认知情感综合征以及缄默症——的神经回路。第二个目标是将这一知识转化为实际的临床干预措施,尽可能预防必要手术中固有的并发症,并采用包括针对受损神经回路相互连接节点的脑调制等方法开发新的治疗途径。