Cerebellar mutism

Patricia L Robertson MD (Dr. Robertson of the University of Michigan has no relevant financial relationships to disclose.)
Karin M Muraszko MD (Dr. Muraszko of the University of Michigan has no relevant financial relationships to disclose.)
Roger J Packer MD, editor. (Dr. Packer of George Washington University; Senior Vice President, Center for Neuroscience and Behavioral Medicine; and Gilbert Endowed Distinguished Professor in Neurofibromatosis and Director, Gilbert Neurofibromatosis Institute and Brain Tumor Institute, Children’s National Health System, has no relevant financial relationships to disclose.)
Originally released November 13, 2003; last updated May 9, 2012; expires May 9, 2015
Notice: This article has expired and is therefore not available for CME credit.

This article includes discussion of cerebellar mutism, mutism and subsequent dysarthria syndrome, oral pharyngeal apraxia and mutism, posterior fossa cerebellar mutism syndrome, posterior fossa syndrome, postoperative mutism, and pseudobulbar syndrome. The foregoing terms may include synonyms, similar disorders, variations in usage, and abbreviations.

Historical note and terminology

The development of mutism, the absence of speech in an awake, noncomatose patient, was first recognized over 20 years ago as a complication of posterior fossa surgery (Fraoli and Guidetti 1975; Hirsch et al 1979; Sakai 1980). Since then, the descriptions of more than 200 cases have contributed to the understanding of this unique constellation of signs and symptoms that has come to be known as the posterior fossa or cerebellar mutism syndrome. This syndrome is characterized by partially reversible decreased production of speech and often mutism, frequently in association with diffuse cerebellar dysfunction (ataxia and axial hypotonia), and a variety of neurobehavioral affective disturbances consisting of prominent emotional lability with irritability and apathy (Fraoli and Guidetti 1975; Hirsch et al 1979; Sakai 1980; Wisoff and Epstein 1984; Rekate et al 1985; Yonemasu 1985; Volcan et al 1986; Ammirati et al 1989; Dietze and Mickle 1990; Ferrante et al 1990; Gaskill and Martin 1991; Nagatani et al 1991; Salvati et al 1991; 1996; Catsman-Berrevoets et al 1992; 1999; Herb and Thyen 1992; Oiwa 1993; Al-Jarallah et al 1994; Asamoto et al 1994; D'Avanzo et al 1994; Kingma et al 1994; Aguiar et al 1995; Dailey et al 1995; Pollack et al 1995; Siffert et al 1995; van Calenbergh et al 1995; Ersahin et al 1996; Jones et al 1996; Mastronardi 1996; Bhatoe 1997; Germano et al 1998; Janssen et al 1998; Liu et al 1998; Turgut 1998; Doxey et al 1999; Gelabert-Gonzalez and Fernandez-Villa 2001; Ildan et al 2002; Wang et al 2002; Mewasingh et al 2003; Paquier et al 2003; Steinbok et al 2003; Ozimek et al 2004; Papavasiliou et al 2004; Robertson et al 2006).

Cerebellar mutism syndrome occurs most often after the surgical resection of posterior fossa tumors, the majority of which are medulloblastoma, but can be seen after trauma, hemorrhage, or ischemic injury involving the cerebellum or brainstem. The onset of symptoms is often delayed until 1 or 2 days after the surgery (Wisoff and Epstein 1984; Ferrante et al 1990; Nagatani et al 1991; Crutchfield et al 1994; Pollack et al 1995; van Calenbergh et al 1995; Salvati et al 1996; Gelabert-Gonzalez and Fernandez-Villa 2001). The first description of mutism after posterior fossa surgery was in regards to several patients who underwent stereotactic lesioning of the cerebellar dentate nucleus for treatment of dyskinesias (Fraoli and Guidetti 1975). Wisoff and Epstein were the first to describe affected patients after midline posterior fossa tumor resection, but they emphasized the emotional features and considered the mutism as part of a syndrome they termed pseudobulbar palsy (Wisoff and Epstein 1984). Rekate and colleagues reported the syndrome in 6 children who underwent posterior fossa tumor surgery and were the first to refer to it as the cerebellar mutism syndrome (Rekate et al 1985). In the same year, Yonemasu noted the same complication in 4 patients who underwent surgery for cerebellar tumors (Yonemasu 1985). This postoperative constellation of signs has also been called the posterior fossa syndrome (Siffert et al 1995). In view of the finding that in many cases the mutism is followed by a period of dysarthric speech, it has also been described as mutism and subsequent dysarthria syndrome (Cakir et al 1994; Dunwoody et al 1997; Doxey et al 1999).

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