1.Mutism after Posterior Fossa Tumor Surgery in a Child: Case Report.
Hyung Jin SHIN ; Yong Gyu PARK ; Jong Woo HAN ; Choong Kun HA
Journal of Korean Neurosurgical Society 1990;19(5):715-719
The authors experienced a case of mutism developed after the posterior fossa tumor surgery in a child. Mutism is a symptom mainly developed by supratentorial lesion in organic form. The possible pathogenesis of mutism after posterior fossa tumor surgery is discussed with a review of 18 additional previously reported cases.
Child*
;
Humans
;
Infratentorial Neoplasms*
;
Mutism*
2.Rostral Midbrain Dysfunction Associated with Hydrocephalus Secondary to Periaqueductal Tumor.
Heon KIM ; Choong Hyun KIM ; Kwoang Hum BAK ; Jae Min KIM ; Nam Kyu KIM
Journal of Korean Neurosurgical Society 1998;27(10):1424-1428
The authors report a case of rostral mesencephalic dysfunction due to obstructive hydrocephalus secondary to periaqueductal tumor who suffered multiple shunt failures and shunt revision. This patient presented with clinical syndromes, including akinetic mutism and diencephalic autonomic epilepsy. He had computed tomography(CT) and magnetic resonance(MR) findings of dilatation of ventricular system with periaqueductal tumor. The anatomical substrates of clinical findings are reviewed. A discussion of the probable mechanism proposes that dilatation of 3rd ventricle and rostral aqueduct sufficiently explains the entire syndrome.
Akinetic Mutism
;
Dilatation
;
Epilepsy
;
Humans
;
Hydrocephalus*
;
Mesencephalon*
3.A Case of Akinetic Mutism Caused by Volume Change of Cerebral Ventricles.
Kyoung Soo LEE ; Oh Young KWON ; Lina LEE ; Ki Jong PARK ; Nack Cheon CHOI ; Byeong Hoon LIM
Journal of the Korean Neurological Association 2002;20(4):414-417
Akinetic mutism is a syndrome caused by various etiologies, and characterized by silent immobility and preserved alertness. The repetitive ventriculoperitoneal shunt for the recurrent hydrocephalus can be a forerunner of that. We present a man with akinetic mutism following two times of ventriculoperitoneal shunt revision. Akinetic mutism of the patient may be caused by the damage on the ascending dopaminergic projections. Symptoms were not alleviated by the normalization of ventricular size but by a large dose of bromocriptine.
Akinetic Mutism*
;
Bromocriptine
;
Cerebral Ventricles*
;
Humans
;
Hydrocephalus
;
Ventriculoperitoneal Shunt
4.A Case of Neurological Complications after Liver Transplantation.
Keun Sik HONG ; Sang Kun LEE ; Sang Yoon KIM ; Kuhn Uk LEE ; Kyung Seok SEO
Journal of the Korean Neurological Association 2000;18(1):116-118
Neurological complications occur frequently in patients undergoing liver transplantation. We report a case of multi-ple neurologic complications including central pontine and extrapontine myelinolysis, seizure, and mutism after liver transplantation. Though the cause would be obscure and multifactorial, the hyponatremia with its rapid correction dur-ing operation and the side effects of the immunosuppressant would be the most probable causes in this case.
Humans
;
Hyponatremia
;
Liver Transplantation*
;
Liver*
;
Mutism
;
Myelinolysis, Central Pontine
;
Seizures
5.A Selective Mutism Arising from First Language Attrition, Successfully Treated with Paroxetine-CBT Combination Treatment.
Agostino SERRA ; Paola DI MAURO ; Claudio ANDALORO ; Luigi MAIOLINO ; Piero PAVONE ; Salvatore COCUZZA
Psychiatry Investigation 2015;12(4):569-572
After immersion in a foreign language, speakers often have difficulty retrieving native-language words and may experience a decrease in its proficiency, this phenomenon, in the non-pathological form, is known as first language attrition. Self-perception of this low native-language proficiency and apprehension occurring when speaking is expected and, may sometimes lead these people to a state of social anxiety and, in extreme forms, can involve the withholding of speech as a primitive tool for self-protection, linking them to selective mutism. We report an unusual case of selective mutism arising from first language attrition in an Italian girl after attending a two-year "German language school", who successfully responded to a paroxetine-cognitive behavioral treatment (CBT) combination treatment.
Anxiety
;
Cognitive Therapy
;
Female
;
Humans
;
Immersion
;
Mutism*
;
Paroxetine
;
Self Concept
6.Akinetic Mutism from Obstructive Hydrocephalus;Successful Treatment with Bromocriptine and Ephedrine.
Young Dae KWON ; Won Ho CHOO ; Jung Hyun CHO ; Seong Cheol KIM ; In Sun HA ; Yong Sung LEE
Journal of Korean Neurosurgical Society 1993;22(1):123-128
The authors report one case of akinetic mutism with obstructive hydrocephalus. The patient suffered from multiple shunt failures and shunt revision. After multiple shunt revision, the patient fell into an akinetic-mute state. She appeared awake but was no response to painful somatosensory, loud auditory or threatening visual stimuli and she required total nursing care. This behavioral syndrome was no response to shunt revision but we were able to successfully treat a case of akinetic mutism after combination theraphy of Bromocryptine and Ephedrine.
Akinetic Mutism*
;
Bromocriptine*
;
Ephedrine*
;
Humans
;
Hydrocephalus
;
Nursing Care
7.Neuroanatomical Mechanism of Cerebellar Mutism After Stroke.
Sekwang LEE ; Yoon Hye NA ; Hyun Im MOON ; Woo Suk TAE ; Sung Bom PYUN
Annals of Rehabilitation Medicine 2017;41(6):1076-1081
Cerebellar mutism (CM) is a rare neurological condition characterized by lack of speech due to cerebellar lesions. CM is often reported in children. We describe a rare case of CM after spontaneous cerebellar hemorrhage. The patient showed mutism, irritability, decreased spontaneous movements and oropharyngeal apraxia. Diffusion tensor imaging revealed significant volume reduction of medial frontal projection fibers from the corpus callosum. In Tracts Constrained by UnderLying Anatomy (TRACULA) analysis, forceps major and minor and bilateral cingulum-angular bundles were not visualized. Cerebello-frontal pathway reconstructed from the FMRIB Software Library showed continuity of fibers, with decreased number of fibers on qualitative analysis. These results suggest that cerebello-frontal disconnection may be a neuroanatomical mechanism of CM. Damage of brain network between occipital lobe, cingulate and cerebellum caused by hemorrhage may also have role in the mechanism of CM in our case.
Akinetic Mutism
;
Apraxias
;
Brain
;
Cerebellum
;
Child
;
Corpus Callosum
;
Diffusion Tensor Imaging
;
Hemorrhage
;
Humans
;
Mutism*
;
Occipital Lobe
;
Stroke*
;
Surgical Instruments
8.Akinetic Mutism and Cognitive-Affective Syndrome Caused by Unilateral PICA Infarction.
Youngsoon YANG ; Jung Eun KIM ; Jung Seok LEE ; Sangyun KIM
Journal of Clinical Neurology 2007;3(4):192-196
A 42-year-old man with left posterior inferior cerebellar artery (PICA) infarction presented with akinetic mutism and cognitive impairment. Initially he suffered from akinetic mutism and MRI-documented infarction in the distribution of the left PICA. Twelve days later he developed cognitive impairment. Neuropsychological tests were performed, with the results corrected for age and education being compared with published Korean norms. Impaired performances were evident on executive function testing, with difficulties in planning, abstract reasoning, set-shifting, and perseveration. Akinetic mutism and cognitive-affective syndrome may be a manifestation of unilateral PICA infarction.
Adult
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Akinetic Mutism*
;
Arteries
;
Education
;
Executive Function
;
Humans
;
Infarction*
;
Neuropsychological Tests
;
Pica*
9.Remote Cerebellar Hemorrhage Presenting with Cerebellar Mutism after Spinal Surgery: An Unusual Case Report.
Halil Murat SEN ; Mustafa GUVEN ; Adem Bozkurt ARAS ; Murat COSAR
Journal of Korean Neurosurgical Society 2017;60(3):367-370
Dural injury during spinal surgery can subsequently give rise to a remote cerebellar hemorrhage (RCH). Although the incidence of such injury is low, the resulting hemorrhage can be life threatening. The mechanism underlying the formation of the hemorrhage is not known, but it is mostly thought to develop after venous infarction. Cerebellar mutism (CM) is a frequent complication of posterior fossa operations in children, but it is rarely seen in adults. The development of CM after an RCH has not been described. We describe the case of a 65-year old female who lost cerebrospinal fluid after inadvertent opening of the dura during surgery. Computerized tomography performed when the patient became unable to speak revealed a bilateral cerebellar hemorrhage.
Adult
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Cerebellum
;
Cerebrospinal Fluid
;
Child
;
Female
;
Hemorrhage*
;
Humans
;
Incidence
;
Infarction
;
Mutism*
;
Spine
10.Transient Cerebellar Mutism after Total Removal of Medulloblastoma in a Child: Case Report.
Chang Bong KONG ; Kyung Bo CHOI ; Hyung Dong KIM
Journal of Korean Neurosurgical Society 2002;32(4):384-386
Transient mutism resolving to cerebellar speech after posterior fossa surgery is a well recognized phenomenon, particularly in pediatric patients. The anatomic basis for this postoperative functional change is unclear, but may reside in the dominant superior cerebellar hemisphere or the medial deep cerebellar nuclei. We report a case of a 9-year-old boy who presented for surgical resection of a medulloblastoma. Preoperatively, his complaint consisted of headache, nausea, vomiting and cerebellar ataxia. He had normal speech. At one day after operation, suddenly he was unable to speech, however, communication through a variety of verbal cues, including sign language was possible. His mutism lasted 12 days and cerebellar dysarthria was slowly resolved.
Cerebellar Ataxia
;
Cerebellar Nuclei
;
Child*
;
Cues
;
Dysarthria
;
Headache
;
Humans
;
Male
;
Medulloblastoma*
;
Mutism*
;
Nausea
;
Sign Language
;
Vomiting