Elsevier

Surgical Neurology

Volume 63, Issue 5, May 2005, Pages 476-479
Surgical Neurology

Mutism
Cerebellar mutism in adults after posterior fossa surgery: a report of 2 cases

https://doi.org/10.1016/j.surneu.2004.06.015Get rights and content

Abstract

Background

Mutism has been associated with injury to midline cerebellar structures secondary to degenerative disease, tumors, hemorrhage, or surgery. Typically, cerebellar mutism syndrome (CMS) has been seen in children and only rarely described in adults after surgery of the posterior fossa. This syndrome typically arises 48 hours after the initiating event and resolves approximately 7 to 8 weeks later. Characteristics of CMS include complete absence of speech without impaired consciousness, other cranial nerve deficits, or long tract signs.

Case Description

The authors report on 2 patients each of whom developed cerebellar mutism after tumor resection using a posterior fossa approach. The first patient underwent gross total resection of a pineal region tumor via a supracerebellar approach. The second patient underwent posterior fossa decompression for a left cerebellar hemispheric renal cell carcinoma metastasis with adjacent hemorrhage. One patient displayed a variant of cerebellar mutism with severe ataxic dysarthria without complete absence of speech, whereas the other demonstrated frank mutism. After neuroimaging studies confirmed the absence of a surgically treatable postoperative cause for the patients' symptoms, they were managed in a supportive fashion (eg, speech therapy) and improved within 3.5 months and 1 year, respectively.

Conclusion

It is paramount that neurosurgeons be aware of cerebellar mutism with regard to its very rare occurrence in adults, its time of onset, and typical self-limiting course.

Introduction

Cerebellar mutism is often considered to be the most extreme form of ataxic dysarthria and is defined as a disturbance of speech and language caused by a lesion to the cerebellum [1], [7], [10]. The spectrum of disturbances can vary from complete absence of speech to hesitant outburst of speech or even monotonous explosive speech [1]. Cerebellar injury secondary to degenerative disease, tumors, hemorrhage, or surgery has been associated with mutism [2]. This condition has rarely been reported in adults as result of injury to cerebellar structures secondary to tumor resection in the posterior cranial fossa.

Section snippets

Case 1

This 33-year-old right-handed female originally presented in 1989 with trouble judging distances and was diagnosed with Parinaud's syndrome. A computed tomographic scan revealed a pineal region tumor. Gross total resection of the tumor revealed a dermoid tumor, and the patient demonstrated improvement in her ophthalmologic dysfunction. Subsequent neuroimaging studies revealed no tumor recurrence until 1998. In 1998, a small amount of tumor recurrence was noted, and at that time, the patient

Discussion

Cerebellar mutism was initially reported in children after surgery in the posterior cranial fossa by Rekate et al [8] and Yonemasu [11] in 1985. The first report of such a phenomenon in an adult was not until 1991 and was secondary to resection of a medulloblastoma in the cerebellar vermis in a 20-year-old male. The diagnosis of cerebellar mutism syndrome requires that the patient have preserved consciousness without cranial nerve deficit or lesion of the long neural pathways. This syndrome has

Conclusions

Cerebellar mutism is a rare postoperative phenomenon that occurs predominantly in children after surgery involving the posterior fossa. It is an even more rare event in adults with fewer than 15 cases described in the literature. However, it is paramount that neurosurgeons be aware of cerebellar mutism. In particular, the typical time of onset for cerebellar mutism is of importance. Cerebellar mutism usually has a self-limiting course and favorable prognosis for resolution. In addition, the

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