Posterior Fossa Syndrome: Review of the Behavioral and Emotional Aspects in Pediatric Cancer Patients

被引:51
作者
Lanier, Jane C. [1 ]
Abrams, Annah N. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Child & Adolescent Psychiat, Boston, MA 02114 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Dept Pediat Hematol & Oncol, Boston, MA USA
关键词
behavior; cerebellar mutism; emotional lability; medulloblastoma; mutism; posterior fossa syndrome; posterior fossa tumors; quality of life; CEREBELLAR MUTISM SYNDROME; TERM-FOLLOW-UP; BRAIN-TUMORS; SUBSEQUENT DYSARTHRIA; TRANSIENT LOSS; CHILDREN; MEDULLOBLASTOMA; SPEECH; REMOVAL; SURGERY;
D O I
10.1002/cncr.30238
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Medulloblastoma, the most common malignant brain tumor of childhood, occurs in the posterior fossa, the part of the intracranial cavity that contains the brainstem and the cerebellum. The cerebellum is involved in many complex aspects of human behavior and function, and when it is disrupted or insulted, this can lead to significant sequelae in children with posterior fossa tumors. A constellation of impairing and distressing symptoms, including mutism, ataxia/hypotonia, and emotional lability, develops in approximately 25% of children after the surgical resection of posterior fossa tumors. These symptoms may impede treatment and frequently require intervention in order for children to be able to participate in their care. The eventual recovery of speech occurs for most, but with slowly improving dysarthria over many months. Behavioral changes and emotional lability also occur. This phenomenon has been classified differently by different investigators over the past 35 years. For the purposes of this article, the term posterior fossa syndrome is used to refer to the neuropsychiatric and behavioral features that compose this condition. The current review summarizes the development of the clinical understanding of this phenomenon with a focus on near-and long-term psychosocial and psychiatric implications. Also, clinical examples of the presentation, management, and lasting implications of this syndrome are provided. This review is intended to be a resource for clinicians who treat affected children. (C) 2016 American Cancer Society.
引用
收藏
页码:551 / 559
页数:9
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