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1.
Medicine (Baltimore) ; 98(32): e16756, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31393392

ABSTRACT

RATIONALE: In some cases, surgery of cerebellopontine angle meningioma (CPAM) might result in multiple cranial nerve injury, which could bring serious impact on the patients, especially when it affects the function of facial muscles and eyeballs. This report describes a successful application of acupuncture for rehabilitation in a patient after surgery for CPAM. PATIENT CONCERNS: A 27-year-old patient presented with limitation of left eye abduction, accompanied with frontal and facial sensory disturbance on the left after resection of the pontocerebellar angle tumor. The patient also suffered from significant anxiety and depression as concomitant symptoms. DIAGNOSES: Based on medical history, clinical symptoms, and magnetic resonance imaging results, the patient was diagnosed with the fourth, fifth, sixth, and seventh cranial nerve injury after surgery for CPAM. INTERVENTIONS: Acupuncture treatment was applied for this patient. One acupuncture session was given every 2 days in 35 days, and the needles were retained for 30 minutes per session. OUTCOMES: After acupuncture treatment, the limitation of left eye abduction had totally recovered. The superficial sensory disturbance in the frontal and facial region was significantly relived. Besides, the scores of Hamilton Anxiety and Depression Scale showed a significant reduction. However, the superficial sensory of the alar and nasolabial groove on the left side still decreased mildly when compared with the right side. CONCLUSION: Acupuncture might be an option for rehabilitation after surgery for CPAM.


Subject(s)
Acupuncture Therapy/methods , Cerebellar Neoplasms/surgery , Cranial Nerve Injuries/rehabilitation , Meningioma/surgery , Adult , Cerebellar Neoplasms/pathology , Cerebellopontine Angle/pathology , Cranial Nerve Injuries/etiology , Humans , Magnetic Resonance Imaging , Male
2.
Ear Nose Throat J ; 94(1): 28, 30-1, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25606833

ABSTRACT

We report a rare case of contralateral hearing loss after vestibular schwannoma excision in a 48-year-old man who underwent surgery via a suboccipital approach for removal of a nearly 2-cm lesion involving the right cerebellopontine angle. Postoperatively, the patient awoke with bilateral deafness, confirmed by both audiometry and spontaneous otoacoustic emissions. The patient was treated aggressively with high-dose intravenous steroids, vitamins E and C, and oxygen. Over the next several months he had gradual recovery of most of the hearing in his left (unoperated) ear. Contralateral hearing loss may develop after vestibular schwannoma excision; multiple pathophysiologic mechanisms for this occurrence have been proposed.


Subject(s)
Cerebellar Neoplasms/surgery , Hearing Loss, Sensorineural/etiology , Neurilemmoma/surgery , Postoperative Complications/etiology , Cerebellopontine Angle , Humans , Male , Middle Aged
3.
Neurocir. - Soc. Luso-Esp. Neurocir ; 22(6): 554-557, nov.-dic. 2011. ilus
Article in Spanish | IBECS | ID: ibc-104740

ABSTRACT

Se analiza el papel de la radiocirugía en un caso de meduloblastoma multirrecidivado del adulto tras dos intervenciones, radioterapia fraccionada, quimioterapia y dos autotrasplantes. Se resalta la precocidad de la respuesta clínico-patológica al tratamiento radioquirúrgico (AU)


The role of radiosurgery after multimodality treatment of recurrent desmoplastic adult medulloblastoma is analyzed. The ultra-early clinical and pathological response of this tumor to adjunctive radiosurgery is stressed (AU)


Subject(s)
Humans , Male , Young Adult , Medulloblastoma/surgery , Radiosurgery/methods , Cerebellar Neoplasms/surgery , Neoplasm Recurrence, Local/surgery
4.
Neuropsychologia ; 49(2): 271-5, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20932984

ABSTRACT

The cerebellum receives signals from, and sends signals to, the parietal cortex and instances of cerebellocerebral diaschisis indicate that some behaviours are controlled through this circuitry. Not all aspects of action control associated with the parietal cortex have been reported in patients with cerebellar damage though. Presented here is a case study of a cerebellar patient whose action deficits appear to be associated with both cerebellar and parietal functions. AM was 27 years old and eight years previously he had an operation to remove a cystic cerebellar tumour. He was tested on his ability to carry out motor imagery, make instructed and spontaneous actions, and intrinsic and extrinsic movements. Similar to ideomotor apraxia patients AM showed an automatic-voluntary dissociation where his motor control was better on spontaneous actions than instructed ones. He also had poor motor imagery timing. However, unlike apraxia patients he was equally poor at controlling body-related and object-related actions and his performance improved without vision. The presence of problems more commonly associated with parietal cortex functions suggest that the cerebellum is involved in a broader spectrum of action abilities than previously thought.


Subject(s)
Cerebellum/physiopathology , Imagination/physiology , Mental Processes/physiology , Movement/physiology , Adult , Analysis of Variance , Cerebellar Neoplasms/surgery , Humans , Male , Neuropsychological Tests , Neurosurgery , Psychomotor Performance
5.
J Neurosurg Pediatr ; 5(5): 428-33, 2010 May.
Article in English | MEDLINE | ID: mdl-20433252

ABSTRACT

Neurogenic stunned myocardium (NSM) is a syndrome of cardiac stunning after a neurological insult. It is commonly observed after aneurysmal subarachnoid hemorrhage but is increasingly being reported after other neurological events. The underlying mechanism of NSM is believed to be a hypothalamic-mediated sympathetic surge causing weakened cardiac contractility and even direct cardiac myocyte damage. The authors report 2 cases of NSM in pediatric patients after acute hydrocephalus. Both patients experienced severe cardiac dysfunction in the acute phase but ultimately had a good neurological outcome and a full cardiac recovery. The identification, treatment, and outcome in 2 rare pediatric cases of NSM are discussed, and the history of the brain-cardiac connection is reviewed.


Subject(s)
Brain Stem Neoplasms/complications , Cerebellar Neoplasms/complications , Glioma/complications , Heart/innervation , Hydrocephalus/complications , Hypothalamus/physiopathology , Medulloblastoma/complications , Myocardial Stunning/diagnosis , Sympathetic Nervous System/physiopathology , Tectum Mesencephali/physiopathology , Adolescent , Brain Stem Neoplasms/diagnosis , Brain Stem Neoplasms/physiopathology , Brain Stem Neoplasms/surgery , Cerebellar Neoplasms/diagnosis , Cerebellar Neoplasms/physiopathology , Cerebellar Neoplasms/surgery , Cerebral Aqueduct/physiopathology , Cerebral Aqueduct/surgery , Child, Preschool , Constriction, Pathologic/complications , Constriction, Pathologic/diagnosis , Constriction, Pathologic/physiopathology , Constriction, Pathologic/surgery , Decompression, Surgical , Female , Follow-Up Studies , Glioma/diagnosis , Glioma/physiopathology , Glioma/surgery , Humans , Hydrocephalus/diagnosis , Hydrocephalus/physiopathology , Hydrocephalus/surgery , Magnetic Resonance Imaging , Medulloblastoma/diagnosis , Medulloblastoma/physiopathology , Medulloblastoma/surgery , Myocardial Stunning/physiopathology , Myocardial Stunning/surgery , Tomography, X-Ray Computed , Ventricular Dysfunction, Left/diagnosis , Ventricular Dysfunction, Left/physiopathology , Ventricular Dysfunction, Left/surgery , Ventriculostomy
6.
Neurocirugia (Astur) ; 20(5): 449-53, 2009 Oct.
Article in Spanish | MEDLINE | ID: mdl-19830367

ABSTRACT

Radionecrosis with brain edema is a complication of radiosurgery. Three female patients harbouring a frontal pole, petrous and parasagital parietoocipital meningiomas respectively who had been treated with LINAC radiosurgery are presented. Those patients developed, between two and eight months later, a severe symptomatic radionecrosis with a huge brain edema resistant to the usual steroid therapy. Only after 40 sessions of hyperbaric oxygen, a good remission of the lesions was obtained. There are few cases reported in the literature with such a good outcome. Consequentely, this therapy must be taken into account to treat this type of radiosurgical complication before considering surgery.


Subject(s)
Brain Edema/therapy , Brain Injuries/therapy , Hyperbaric Oxygenation , Radiation Injuries/therapy , Radiosurgery/adverse effects , Aged , Brain Damage, Chronic/etiology , Brain Damage, Chronic/prevention & control , Brain Edema/etiology , Brain Edema/pathology , Brain Injuries/etiology , Brain Injuries/pathology , Cerebellar Neoplasms/surgery , Cerebellopontine Angle/pathology , Cerebellopontine Angle/radiation effects , Endothelium, Vascular/pathology , Endothelium, Vascular/radiation effects , Female , Humans , Magnetic Resonance Imaging , Meningeal Neoplasms/surgery , Meningioma/surgery , Middle Aged , Necrosis , Parietal Lobe/pathology , Parietal Lobe/radiation effects , Radiation Injuries/etiology , Radiation Injuries/pathology , Treatment Outcome
7.
Neurocir. - Soc. Luso-Esp. Neurocir ; 20(5): 449-453, sept.-oct. 2009. ilus
Article in Spanish | IBECS | ID: ibc-76912

ABSTRACT

La radio necrosis y el edema cerebral son complicaciones asociadas a la radiocirugía. Presentamos los casos de tres pacientes tratadas con radiocirugía mediante acelerador lineal, de un meningioma de polo frontal izquierdo, peñasco y para sagital parietooccipital, respectivamente, que desarrollaron, entre dos y ocho meses más tarde, lesiones de tipo radio necrótico con extenso edema peritumoral que resultaron resistentes al tratamiento con esteroides y que se han resuelto con la administración de 40 sesiones de oxígeno hiperbárico. Son pocos los casos publicados hasta ahora en la literatura con tan excelentes resultados, por lo que consideramos un hecho a tener muy en cuenta ante las posibles complicaciones de este tipo que puedan presentarse en el transcurso de la práctica radioquirúrgica antes de recurrir a la cirugía (AU)


Radionecrosis with brain edema is a complication of radiosurgery. Three female patients harbouring a frontal pole, petrous and parasagital parietoocipital meningiomas respectively who had been treated with LINAC radiosurgery are presented. Those patients developed, between two and eight months later, a severe symptomatic radionecrosis with a huge brain edema resistant to the usual steroid therapy. Only after 40 sessions of hyperbaric oxygen, a good remission of the lesions was obtained. There are few cases reported in the literature with such a good outcome. Consequentely, this therapy must be taken into account to treat this type of radiosurgical complication before considering surgery (AU)


Subject(s)
Humans , Female , Middle Aged , Brain Edema/therapy , Brain Injuries, Traumatic/therapy , Hyperbaric Oxygenation , Radiation Injuries/therapy , Radiosurgery/adverse effects , Brain Damage, Chronic/etiology , Brain Damage, Chronic/prevention & control , Brain Edema/etiology , Brain Edema/pathology , Brain Injuries, Traumatic/etiology , Brain Injuries, Traumatic/pathology , Cerebellar Neoplasms/surgery , Cerebellopontine Angle/pathology , Endothelium, Vascular/pathology , Endothelium, Vascular/radiation effects , Magnetic Resonance Imaging , Meningeal Neoplasms/surgery , Meningioma/surgery , Necrosis , Parietal Lobe/pathology , Parietal Lobe/radiation effects , Radiation Injuries/etiology , Radiation Injuries/pathology , Treatment Outcome
8.
J Child Neurol ; 24(7): 861-4, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19189936

ABSTRACT

Essential tremor is a long-recognized and common movement disorder, yet controversy still surrounds its pathophysiology. The olivo-cerebello-thalamo-cortical pathway has been implicated in the genesis of essential tremor, and the inferior olive has been considered the central oscillator driving the peripheral tremor. We present the case of a patient who developed essential tremor ipsilateral to cerebellar hemispherectomy and propose that the central oscillator in patients with essential tremor may not be the inferior olive in all cases, but rather the nucleus ventralis intermedius of the thalamus.


Subject(s)
Cerebellar Neoplasms/surgery , Cerebellum/surgery , Essential Tremor/etiology , Essential Tremor/physiopathology , Periodicity , Thalamus/physiopathology , Astrocytoma/pathology , Astrocytoma/surgery , Cerebellar Neoplasms/pathology , Cerebellum/pathology , Child , Diagnosis, Differential , Essential Tremor/pathology , Female , Functional Laterality , Humans , Magnetic Resonance Imaging , Thalamus/pathology
10.
Otol Neurotol ; 28(4): 541-5, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17529854

ABSTRACT

OBJECTIVE: To investigate the use of transtympanic electrocochleography (TT-ECochG) analyzed on-line by a detector strategy software that made possible automatic extraction of TT-ECochG components intraoperatively in real-time domain. PATIENTS: Fifteen patients with cerebellopontine angle tumor among 50 patients were included in this study. INTERVENTION: All subjects were operated on via middle fossa or retrosigmoid approach. Pure-tone average (PTA) was measured at 0.5, 1.0, and 2.0 kHz, and calculations were performed before and after surgery. Auditory function was monitored intraoperatively via TT-ECochG, and analyzed data were displayed on-line. MAIN OUTCOME MEASURES: TT-ECochG changes in morphology were described. Postoperative PTA elevation level correlated with TT-ECochG morphology changes occurring intraoperatively. RESULTS: Analyzed on-line, TT-ECochG data were displayed as first negative peak of compound action potential amplitude and latency in time domain every 3 to 5 seconds. A good correlation between postoperative PTA elevation and TT-ECochG morphology changes was showed (Spearman rank test, R = +0.93; t(N-2) = 9.00; p < 0.0001). CONCLUSION: TT-EcochG seemed to effectively mirror even minimal changes in auditory function during intraoperative monitoring in real-time domain. Developed strategy of on-line analysis makes the intraoperative hearing status assessment faster and easier.


Subject(s)
Audiometry, Evoked Response , Cerebellar Neoplasms/surgery , Cerebellopontine Angle/surgery , Hearing/physiology , Tympanic Membrane/physiology , Acoustic Stimulation , Adult , Aged , Evoked Potentials, Auditory/physiology , Female , Humans , Male , Middle Aged , Monitoring, Intraoperative , Potentiometry
11.
Surg Neurol ; 66(1): 18-25, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16793430

ABSTRACT

OBJECTIVE: Cerebellar mutism (CM) is a postoperative complication of mainly pediatric posterior fossa surgery. Multiple theories exist for explaining this phenomenon. We have made an attempt to further understand this entity given a particularly interesting case as it relates to multiple pathophysiologic pathways. METHODS: We have reviewed the details surrounding a particularly interesting case of CM. A retrospective analysis of this patient's clinical history and recovery is described. An extensive literature review has been performed in conjunction with an attempt to help elucidate details and a better understanding of CM. RESULTS: A thorough analysis of existing theories as to the pathophysiologic mechanism of CM has been performed as it relates to the details of this particular case. A case is described in which a child exhibiting CM abruptly improved and made a relatively quick recovery after the triggering of the melodic speech pathway by way of watching and beginning to sing along with a video. It appears that this incident involving a familiar song catalyzed various speech pathways, which apparently were in some state of shock. This phenomenon seems to be a temporary entity involving not only the mechanical coordination of speech production, but also the initiation of speech itself. CONCLUSIONS: Evidence exists for a pathophysiologic pathway for speech by way of coordinating phonation and articulation. In addition, there seems to exist a pathway by which the initiation of speech may be altered or halted by posterior fossa pathology, namely, vermian or dentate nuclear injury. In particular to this case, we found that the incidental appreciation of other forms of speech, melodic in this instance, may be the key to help stimulate and accelerate the recovery from CM.


Subject(s)
Cerebellar Diseases/physiopathology , Cerebellar Neoplasms/physiopathology , Medulloblastoma/physiopathology , Mutism/physiopathology , Acoustic Stimulation/methods , Cerebellar Diseases/etiology , Cerebellar Diseases/rehabilitation , Cerebellar Neoplasms/complications , Cerebellar Neoplasms/surgery , Child, Preschool , Humans , Hydrocephalus/complications , Hydrocephalus/physiopathology , Hydrocephalus/surgery , Male , Medulloblastoma/complications , Medulloblastoma/surgery , Music Therapy , Mutism/etiology , Mutism/rehabilitation , Neural Pathways/physiopathology , Neurosurgical Procedures/adverse effects , Recovery of Function
12.
Neurosurgery ; 58(4): E789; discussion E789, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16575298

ABSTRACT

OBJECTIVE AND IMPORTANCE: We present a rare case of very long-term medulloblastoma relapse in an adult patient and discuss the pattern of recurrence and metabolic imaging of the tumor. CLINICAL PRESENTATION: A 45-year-old man was referred for evaluation of a frontobasal midline tumor 21 years after treatment of a cerebellar medulloblastoma by surgery followed by chemotherapy and craniospinal radiotherapy. Magnetic resonance images were suggestive of a meningioma. Several hypotheses were discussed, such as other radio-induced tumors, sarcomas, high-grade gliomas, or lymphomas (previous chemotherapy) and even recurrence of medulloblastoma. Preoperative exploration included H magnetic resonance single-voxel spectroscopy (35 and 135 ms echo time), diffusion imaging, and perfusion magnetic resonance imaging. INTERVENTION: On magnetic resonance spectroscopy, N-acetyl-aspartate and an elevated choline/creatine ratio were retrieved, with a huge unidentified peak at 1.27 parts per million (ppm). Myoinositol signal was present at both echo times. On diffusion imaging, the tumor appeared hyperintense, with a low apparent diffusion coefficient value of 0.689. In the perfusion study, the maximal relative cerebral blood volume was 2. Metabolic imaging favored the diagnosis of medulloblastoma over the initially suspected diagnosis of meningioma. The patient underwent complete removal of the tumor that was confirmed to be a metastasis of his primary medulloblastoma. The postoperative course was uneventful, and complementary courses of radiotherapy and chemotherapy were planned. CONCLUSION: Late relapse should be considered, even after several decades, on occurrence of a second intracranial tumor in this context. Our observation validates the clinical interest of preoperative metabolic imaging for brain tumors with distinctive pattern.


Subject(s)
Cerebellar Neoplasms/diagnosis , Medulloblastoma/diagnosis , Meningeal Neoplasms/diagnosis , Meningioma/diagnosis , Cerebellar Neoplasms/surgery , Diagnosis, Differential , Diffusion Magnetic Resonance Imaging/methods , Humans , Magnetic Resonance Spectroscopy/methods , Male , Medulloblastoma/surgery , Meningeal Neoplasms/surgery , Meningioma/surgery , Middle Aged , Preoperative Care/methods , Protons , Recurrence
13.
J Neurosci ; 25(27): 6362-71, 2005 Jul 06.
Article in English | MEDLINE | ID: mdl-16000626

ABSTRACT

Functional imaging studies of olfaction have consistently reported odorant-induced activation of the cerebellum. However, the cerebellar role in olfaction remains unknown. We examined the olfactory and olfactomotor abilities of patients with unilateral cerebellar lesions, comparing performance within subjects across nostrils, as well as between subjects with age-matched and young controls. Regarding olfactory performance, initial testing revealed that patients had a contralesional impairment in olfactory identification but not olfactory detection threshold. However, when tested under conditions that prevented compensatory sniffing strategies, the patients also exhibited a contralesional olfactory detection impairment. Regarding olfactomotor function, a healthy olfactomotor system generates sniffs that are (1) sufficiently vigorous and (2) inversely proportional to odorant concentration in sniff mean airflow velocity, maximum airflow velocity, volume, and duration. Patients' sniffs were lower in overall airflow velocity and volume in comparison with control participants. Furthermore, reduced sniff velocity predicted poorer detection thresholds in patients. Finally, whereas young controls used concentration-dependent sniffs, there was a trend in that direction only for age-matched controls. Patients used sniffs that were concentration invariant. In conclusion, cerebellar lesions impacted olfactory and olfactomotor performance. These findings strongly implicate an olfactocerebellar pathway prominent in odor identification and detection that functionally connects each nostril primarily to the contralateral cerebellum.


Subject(s)
Agnosia/physiopathology , Cerebellum/injuries , Dominance, Cerebral , Inhalation/physiology , Nasal Cavity/physiopathology , Odorants , Olfaction Disorders/physiopathology , Olfactory Pathways/physiopathology , Pulmonary Ventilation/physiology , Acoustic Stimulation , Adult , Age Factors , Aged , Case-Control Studies , Cerebellar Neoplasms/complications , Cerebellar Neoplasms/pathology , Cerebellar Neoplasms/surgery , Cerebellum/pathology , Dose-Response Relationship, Drug , Humans , Likelihood Functions , Magnetic Resonance Imaging , Male , Middle Aged , Olfaction Disorders/etiology , Sensory Thresholds , Smoking , Stroke/complications , Stroke/pathology
14.
Klin Padiatr ; 217(3): 153-7, 2005.
Article in German | MEDLINE | ID: mdl-15858707

ABSTRACT

Supratentorial primitive neuroectodermal tumors (stPNETs) are malignant tumors. We saw within three years six children with stPNETs. In four of the six children radical resection could be achieved. All had craniospinal irradiation and chemotherapy according to the HIT-91 protocol. The two children with incomplete resection died due to tumor progression after 7 and 10 months. Two of the 4 children with complete tumor resection had local relapses 8 months after diagnosis and died after 14 and 18 months. One child had a diffuse meningeal relapse 12 months after diagnosis. Despite (high-dose) systemic chemotherapy and intraventricular mafosfamide, he died 21 months after diagnosis due to tumor although remission could be achieved. Only one child is still in remission 86 months after diagnosis.


Subject(s)
Brain Neoplasms , Cerebellar Nuclei , Corpus Callosum , Frontal Lobe , Neuroectodermal Tumors , Occipital Lobe , Parietal Lobe , Temporal Lobe , Thalamus , Brain Neoplasms/drug therapy , Brain Neoplasms/mortality , Brain Neoplasms/radiotherapy , Brain Neoplasms/surgery , Brain Stem Neoplasms/secondary , Cerebellar Neoplasms/mortality , Cerebellar Neoplasms/surgery , Child , Child, Preschool , Combined Modality Therapy , Disease Progression , Humans , Male , Mesencephalon , Neoplasm Recurrence, Local , Neuroectodermal Tumors/drug therapy , Neuroectodermal Tumors/mortality , Neuroectodermal Tumors/radiotherapy , Neuroectodermal Tumors/surgery , Prognosis , Remission Induction , Time Factors
15.
Surg Neurol ; 63(4): 307-15; discussion 315-6, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15808704

ABSTRACT

OBJECTIVE: The study aims to elucidate the advance of diagnosis and surgical treatment of brainstem hemangioblastomas (BSHs). METHODS: The data of the following patients treated in one institute were retrospectively analyzed: (1) patients with a single tumor on the brainstem which was verified by surgery and pathology; (2) patients without von Hippel-Lindau disease or multiple hemangioblastomas. RESULTS: Thirty-three patients with BSHs were identified, accounting for 15.5% of all intracranial hemangioblastomas surgically treated from August 1989 to May 2002 in Huashan Hospital. There were 17 males and 16 females. The patients were aged from 16 to 65 years with an average age of 45 years. The clinical manifestations were nonspecific. Magnetic resonance imaging and digital subtraction angiography were the major diagnostic modalities. Tumors were located on oblongata (14), ponto-oblongata (9), pons (6), and cervicomedulla (4). Tumors were solid in 29 cases, cyst in 4 cases, and had a small size in 5 (< or =3 cm), large in 19 (3.1-4 cm), and giant in 9 (>4 cm). Extra-brainstem (EBS) type (including the fourth-ventricle hemangioblastomas) was seen in 25 cases, and intrabrainstem (IBS) type in 8 cases. Preoperative embolization was performed in 12 cases since 1996. Mild hypothermia with or without hypotension was done during the operation in 10 cases. Total tumor removal was achieved in 31 patients (94%), and incomplete removal in 2 cases. Two patients with EBS type and giant solid tumors died after operation. Follow-up study (range, 1-12 years; mean, 5 years) was available in 31 patients. Karnofsky performance scale scores were > or =80 in 25 patients (80.6%), 60 to 70 in 4 patients (12.9%), and 40 to 50 in 2 patients (6.5%). CONCLUSION: Two types of BSHs can be identified. Patients with cystic IBS type could obtain excellent outcome after operations. Patients with giant or large solid BSHs remain a challenge to neurosurgeons. A combined strategy of preoperative embolization, mild hypothermia with or without hypotension, microsurgical technique, and intensive perioperative management are mandatory for removal of these kinds of tumors with acceptable morbidity and mortality.


Subject(s)
Cerebellar Neoplasms/surgery , Cerebellar Neoplasms/therapy , Embolization, Therapeutic , Hemangioblastoma/surgery , Hemangioblastoma/therapy , Adolescent , Adult , Aged , Cerebellar Neoplasms/pathology , Combined Modality Therapy , Female , Hemangioblastoma/pathology , Humans , Hyperthermia, Induced , Hypotension , Male , Middle Aged , Prognosis , Retrospective Studies , Treatment Outcome
16.
Brain Lang ; 92(2): 153-67, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15629489

ABSTRACT

The present study investigated dysarthric symptoms in children with cerebellar tumors. Ten children with cerebellar tumors and 10 orthopedic control children were tested prior and one week after surgery. Clinical dysarthric symptoms were quantified in spontaneous speech. Syllable durations were analyzed in syllable repetition and sentence production tasks. Localization of the cerebellar lesions were defined after manual transfer from individual 2D-MR images onto 3D images of a spatially normalized healthy brain. Cerebellar children showed few and mild clinical signs of dysarthria. No difference was present in the sentence production task compared to controls. In five cerebellar children, syllables were prolonged in the syllable repetition task after surgery. Syllable duration normalized in an additional four-week session in all but one case. The MR-analysis showed that superior paravermal cerebellar areas likely involved in dysarthria in adults (paravermal lobules HVI, Crus I) were not significantly affected. In children, speech impairments appear to be rare after cerebellar surgery because tumors most commonly affect posterior-inferior and medial parts of the cerebellum while critical cerebellar regions are likely spared. The results suggest a similar localization of speech functions in the cerebellum in children and adults.


Subject(s)
Astrocytoma/epidemiology , Cerebellar Neoplasms/epidemiology , Dysarthria/epidemiology , Dysarthria/physiopathology , Acoustic Stimulation , Adolescent , Astrocytoma/pathology , Astrocytoma/surgery , Cerebellar Neoplasms/pathology , Cerebellar Neoplasms/surgery , Child , Dysarthria/pathology , Female , Humans , Incidence , Magnetic Resonance Imaging , Male , Medulloblastoma/epidemiology , Medulloblastoma/pathology , Medulloblastoma/surgery , Neuroma, Acoustic/epidemiology , Neuroma, Acoustic/pathology , Neuroma, Acoustic/surgery , Prospective Studies , Speech , Speech Perception
17.
J Clin Oncol ; 22(24): 4881-7, 2004 Dec 15.
Article in English | MEDLINE | ID: mdl-15611503

ABSTRACT

PURPOSE: To evaluate the feasibility of and response rate to an intensified induction chemotherapy regimen for young children with newly diagnosed high-risk or disseminated medulloblastomas. PATIENTS AND METHODS: From January 1997 to March 2003, 21 patients with high-risk or disseminated medulloblastoma were enrolled. After maximal surgical resection, patients were treated with five cycles of vincristine (0.05 mg/kg/wk x three doses per cycle for three cycles), cisplatin (3.5 mg/kg per cycle), etoposide (4 mg/kg/d x 2 days per cycle), cyclophosphamide (65 mg/kg/d x 2 days per cycle) with mesna, and methotrexate (400 mg/kg per cycle) with leucovorin rescue. Following induction chemotherapy, eligible patients underwent a single myeloablative chemotherapy cycle with autologous stem-cell rescue. RESULTS: Significant toxicities of this intensified regimen, including gastrointestinal and infectious toxicities, are described. Among the 21 patients enrolled, there were 17 complete responses (81%), two partial responses, one stable disease, and one progressive disease. The 3-year event-free survival and overall survival are 49% (95% CI, 27% to 72%) and 60% (95% CI, 36% to 84%), respectively. CONCLUSION: This intensified induction chemotherapy regimen is feasible and tolerable. With the majority of patients with disseminated medulloblastoma having M2 or M3 disease at diagnosis, the encouraging high response rate of this intensified induction regimen suggests that such an addition of methotrexate should be explored in future studies.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cerebellar Neoplasms/drug therapy , Medulloblastoma/drug therapy , Cerebellar Neoplasms/pathology , Cerebellar Neoplasms/surgery , Child , Child, Preschool , Cisplatin/administration & dosage , Cisplatin/adverse effects , Cyclophosphamide/administration & dosage , Cyclophosphamide/adverse effects , Disease Progression , Disease-Free Survival , Dose-Response Relationship, Drug , Etoposide/administration & dosage , Etoposide/adverse effects , Female , Humans , Leucovorin/administration & dosage , Male , Medulloblastoma/pathology , Medulloblastoma/surgery , Mesna/administration & dosage , Methotrexate/administration & dosage , Methotrexate/adverse effects , Risk Factors , Stem Cell Transplantation , Transplantation, Autologous , Treatment Outcome , Vincristine/administration & dosage , Vincristine/adverse effects
18.
Strahlenther Onkol ; 179(8): 509-20, 2003 Aug.
Article in English | MEDLINE | ID: mdl-14509949

ABSTRACT

BACKGROUND: Treatment of childhood low-grade gliomas is a challenging issue owing to their low incidence and the lack of consensus about "optimal" treatment approach. MATERIAL AND METHODS: Reports in the literature spanning 60 years of radiation therapy, including orthovoltage, megavoltage and recently modern high-precision treatments, were reviewed with respect to visual function, survival, prognostic factors, dose prescriptions, target volumes, and treatment techniques. Based on these experiences, future strategies in the management of childhood low-grade glioma are presented. RESULTS: Evaluation of published reports is difficult because of inconsistencies in data presentation, relatively short follow-up in some series and failure to present findings and results in a comparable way. Even with the shortcomings of the reports available in the literature, primarily concerning indications, age at treatment, dose response, timing and use of "optimal" treatment fields, radiation therapy continues to play an important role in the management of these tumors achieving long-term survival rates up to 80% or more. Particularly in gliomas of the visual pathway, high local tumor control and improved or stable visual function is achieved in approximately 90% of cases. Data on dose-response relationships recommend dose prescriptions between 45 and 54 Gy with standard fractionation. There is consensus now to employ radiation therapy in older children in case of progressive disease only, regardless of tumor location and histologic subtype. In younger children, the role of radiotherapy is unclear. Recent advances in treatment techniques, such as 3-D treatment planning and various "high-precision" treatments achieved promising initial outcome, however with limited patient numbers and short follow-ups. CONCLUSIONS: Radiation therapy is an effective treatment modality in children with low-grade glioma regarding tumor control and improvement and/or preservation of neurologic function or vision, respectively. More prospective studies are needed to address the impact of modern radiation therapy technologies (including intensity-modulated radiotherapy) on outcome especially in the very young and to define the role of radiation therapy as a part of a comprehensive treatment approach. The forthcoming prospective trial SIOP/GPOH LGG RT 2003 is addressing this issue.


Subject(s)
Brain Neoplasms/radiotherapy , Glioma/radiotherapy , Neurofibromatoses/radiotherapy , Optic Nerve Neoplasms/radiotherapy , Adolescent , Adult , Age Factors , Astrocytoma/drug therapy , Astrocytoma/radiotherapy , Astrocytoma/surgery , Brachytherapy , Brain Neoplasms/drug therapy , Brain Neoplasms/mortality , Brain Neoplasms/surgery , Cerebellar Neoplasms/drug therapy , Cerebellar Neoplasms/radiotherapy , Cerebellar Neoplasms/surgery , Child , Child, Preschool , Clinical Trials as Topic , Combined Modality Therapy , Disease-Free Survival , Dose Fractionation, Radiation , Dose-Response Relationship, Radiation , Follow-Up Studies , Glioma/drug therapy , Glioma/mortality , Glioma/surgery , Humans , Hypothalamus , Medulloblastoma/drug therapy , Medulloblastoma/radiotherapy , Medulloblastoma/surgery , Neurofibromatoses/drug therapy , Neurofibromatoses/mortality , Neurofibromatoses/surgery , Optic Chiasm , Optic Nerve Neoplasms/drug therapy , Optic Nerve Neoplasms/mortality , Optic Nerve Neoplasms/surgery , Postoperative Care , Prognosis , Proton Therapy , Radiotherapy Dosage , Radiotherapy Planning, Computer-Assisted , Radiotherapy, Conformal , Retrospective Studies , Survival Analysis , Time Factors , Vision, Ocular , Visual Pathways
20.
Ann Nucl Med ; 15(2): 157-60, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11448076

ABSTRACT

A 7-year-old boy developed mutism after surgery for cerebellar medulloblastoma. Postoperative magnetic resonance imaging (MRI) showed atrophy of the cerebellar vermis and both cerebellar hemispheres, predominantly on the right side. Single photon emission computed tomography (SPECT) with technetium-99m-ethyl cysteinate dimer (Tc-99m ECD) revealed decreased cerebral blood flow (CBF) in the bilateral thalami, bilateral medial frontal lobes, and left temporal lobe in addition to the cerebellar vermis and both cerebellar hemispheres when mutism was manifest, indicating the existence of bilateral crossed cerebello-cerebral diaschisis (BCCCD). Circulatory disturbance in both cerebellar hemispheres secondary to tumor resection probably caused BCCCD in both cerebral hemispheres, predominantly in the left, via the dentatothalamocortical pathway (DTCP). With recovery of his mutism, CBF increased in the right thalamus, bilateral medial frontal lobes and left temporal lobe. Thus BCCCD was improved, with only a slight decrease in CBF still persisting in the left thalamus. The mechanism of mutism may have involved damage to the cerebellar vermis (the site of incision at operation), the left dentate nucleus (heavily infiltrated by the tumor) and the right dentate nucleus of the cerebellum (affected by circulatory disturbance secondary to acute postoperative edema). The SPECT findings suggested that mutism was associated with BCCCD-induced cerebral circulatory and metabolic hypofunction in the supplementary motor area mediated via the DTCP.


Subject(s)
Cerebellar Neoplasms/surgery , Cerebellum/blood supply , Cerebellum/injuries , Cerebrovascular Circulation , Cysteine/analogs & derivatives , Medulloblastoma/surgery , Mutism/diagnostic imaging , Mutism/etiology , Postoperative Complications/diagnostic imaging , Child , Humans , Male , Organotechnetium Compounds , Radiopharmaceuticals , Tomography, Emission-Computed, Single-Photon
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