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1.
Mov Disord ; 38(11): 2053-2063, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37638533

ABSTRACT

BACKGROUND: Parkinson's disease (PD) is a heterogeneous neurodegenerative disorder characterized by motor and nonmotor symptoms. Several features have prognostic importance and have been used as key indicators for identifying clinical subtypes. However, the symptom-based classification approach has limitations with respect to the stability of the obtained subtypes. OBJECTIVES: The purpose of this study was to identify subtypes of PD using nuclear imaging biomarkers targeting the cardiac sympathetic nervous and nigro-striatal systems and to compare patterns of cortical morphological change among obtained subtypes. METHODS: We performed unbiased hierarchical cluster analysis using 123 I-metaiodobenzylguanidine cardiac scintigraphy and 123 I-N-(3-fluoropropyl)-2ß-carbomethoxy-3ß-(4-iodophenyl) nortropane single photon emission computed tomography data for 56 patients with PD. We compared clinical characteristics and the patterns of cortical atrophy in the obtained clusters. RESULTS: Three clusters were identified and showed distinct characteristics in onset ages and dopamine-replacement therapy and deep brain stimulation requirements. According to the characteristics, clusters were classified into two subtypes, namely, "cardio-cortical impairment (CC)" and "dopaminergic-dominant dysfunction (DD)" subtype. The three clusters were named according to subtype and time since onset in which 14 patients were classified as "early DD," 25 as "advanced DD," and 17 as "early CC." Compared with the early DD subtype, the early CC subtype showed parietal-dominant diffuse cortical atrophy and the advanced DD subtype showed left-side predominant mild cortical atrophy. CONCLUSIONS: Nuclear imaging biomarker-based classification can be used to identify clinically and pathologically relevant PD subtypes with distinct disease trajectories. © 2023 International Parkinson and Movement Disorder Society.


Subject(s)
Parkinson Disease , Humans , Parkinson Disease/diagnosis , Radionuclide Imaging , Tomography, Emission-Computed, Single-Photon/methods , Corpus Striatum/metabolism , Atrophy , Tropanes , Dopamine Plasma Membrane Transport Proteins/metabolism
4.
J Clin Neurosci ; 44: 164-168, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28676310

ABSTRACT

We retrospectively investigated the effects of subthalamic nucleus stimulation (STN-DBS) on new postoperative onset of cognitive decline and prognostic factors for advanced Parkinson's disease (PD). We studied 39 PD patients who had received bilateral STN-DBS. Clinical symptoms, cognitive function, psychiatric function, and health-related quality of life (HRQOL) were assessed before and six months after surgery. Based on the results of neuropsychological examinations six months after the surgery, the subjects were divided into those with and those without cognitive decline. We compared pre- and post-operative assessments between the two groups. Prognostic factors were investigated using multiple logistic regression analyses. Seven patients had cognitive decline six months after the operation (17.9%); they were significantly older than those without cognitive decline. Preoperative neuropsychological examinations revealed impairments in language and executive function. No differences were found in clinical symptoms. Patients with cognitive decline had significantly worse apathy scale scores. The HRQOL revealed significant declines in the Mental Component Summary (MCS), vitality, and mental health (MH) domains. Postoperative comparisons revealed novel significant differences in activities of daily living in the "on" and "off" states and in daytime drowsiness. Preoperative differences seen in the MCS and vitality indices were no longer present. Word fluency, and apathy scale and MH scores were independent preoperative prognostic factors for cognitive decline. New postoperative onset of cognitive decline due to STN-DBS affected activities of daily living and psychiatric function. Preoperative non-motor symptoms may be prognostic factors for new onset of cognitive decline.


Subject(s)
Cognitive Dysfunction/etiology , Deep Brain Stimulation/adverse effects , Parkinson Disease/therapy , Postoperative Complications , Activities of Daily Living , Aged , Executive Function , Female , Humans , Male , Middle Aged , Parkinson Disease/pathology , Quality of Life , Subthalamic Nucleus/physiopathology
5.
Neurol Med Chir (Tokyo) ; 53(7): 455-66, 2013.
Article in English | MEDLINE | ID: mdl-23883556

ABSTRACT

We retrospectively analyzed 15 years experience of awake surgeries for neuroepithelial tumors in Tohoku University. Awake surgeries mostly for language mapping were performed for 42 of 681 newly diagnosed cases (6.2%) and 59 of 985 surgeries including for recurrence (6.0%). When the same histologies and locations as cases resected under awake condition are selected from the parent population treated by radical resection, awake surgeries were most frequently performed for 14 of 55 newly diagnosed cases (25.5%) and 14 of 62 surgeries (22.6%) with grade II gliomas. In the results, 8 of 59 surgeries (13.6%) could not achieve complete language monitoring until the final stage of tumor resection, considered as failed awake surgery. Gross total resection was accomplished in 20 of 42 newly diagnosed cases (47.6%) and 32 of 59 surgeries (54.2%). Mortality rate was 0%. Late severe deficits were observed in 2 of 42 newly diagnosed cases (4.8%) and 3 of 59 surgeries (5.1%). Negative language mapping cases did not suffer severe deficits in both early and late stages. In contrast, high incidence of severe deficits, 3 as early and 2 as late of 8 cases, were identified with failed awake surgery. The overall survival of patients treated by awake surgery compared favorably with those treated without stimulation mapping and with stimulation mapping under general anesthesia. Awake surgery may contribute to improve the outcome of gliomas near eloquent areas by maximizing the tumor resection and minimizing the surgical morbidity.


Subject(s)
Anesthesia/methods , Brain Mapping/methods , Brain Neoplasms/physiopathology , Brain Neoplasms/surgery , Neoplasms, Neuroepithelial/physiopathology , Neoplasms, Neuroepithelial/surgery , Speech/physiology , Wakefulness , Adult , Aged , Cerebral Cortex/pathology , Cerebral Cortex/surgery , Electric Stimulation , Female , Hospitals, University , Humans , Japan , Magnetic Resonance Imaging , Male , Middle Aged , Motor Cortex/physiopathology , Motor Cortex/surgery , Prognosis , Reoperation , Retrospective Studies , Young Adult
6.
J Neurosurg Pediatr ; 7(5): 522-6, 2011 May.
Article in English | MEDLINE | ID: mdl-21529193

ABSTRACT

This 13-year-old boy with a history of cranial irradiation for the CNS recurrence of acute lymphocytic leukemia developed a glioblastoma in the right cerebellum. Resection and chemo- and radiotherapy induced remission of the disease. However, recurrence was noted in the brainstem region 8 months later. Because no effective treatment was available for this recurrent lesion, the authors decided to use convection-enhanced delivery (CED) to infuse nimustine hydrochloride. On stereotactic insertion of the infusion cannula into the brainstem lesion, CED of nimustine hydrochloride was performed with real-time MR imaging to monitor the co-infused chelated gadolinium. The patient's preinfusion symptom of diplopia disappeared after treatment. Follow-up MR imaging revealed the response of the tumor. The authors report on a case of recurrent glioblastoma infiltrating the brainstem that regressed after CED of nimustine hydrochloride.


Subject(s)
Antineoplastic Agents/administration & dosage , Brain Stem Neoplasms/drug therapy , Cerebellar Neoplasms/drug therapy , Convection , Drug Delivery Systems/instrumentation , Glioblastoma/drug therapy , Neoplasm Recurrence, Local/drug therapy , Nimustine/administration & dosage , Adolescent , Antineoplastic Agents/adverse effects , Brain Stem Neoplasms/pathology , Brain Stem Neoplasms/surgery , Cerebellar Neoplasms/pathology , Cerebellar Neoplasms/surgery , Chemotherapy, Adjuvant , Cranial Irradiation , Follow-Up Studies , Glioblastoma/pathology , Glioblastoma/surgery , Humans , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Magnetic Resonance Imaging , Male , Neoplasm Recurrence, Local/pathology , Neoplasm Recurrence, Local/surgery , Neoplasms, Radiation-Induced/drug therapy , Neoplasms, Radiation-Induced/pathology , Neoplasms, Radiation-Induced/surgery , Neoplasms, Second Primary/drug therapy , Neoplasms, Second Primary/pathology , Neoplasms, Second Primary/surgery , Nimustine/adverse effects , Precursor Cell Lymphoblastic Leukemia-Lymphoma/radiotherapy , Stereotaxic Techniques
7.
Neurol Med Chir (Tokyo) ; 49(12): 608-11, 2009 Dec.
Article in English | MEDLINE | ID: mdl-20035139

ABSTRACT

A 57-year-old man suffered from dizziness for about one year and truncal ataxia for about one month. Magnetic resonance imaging demonstrated a cystic tumor with a homogeneously enhanced mural nodule located in the cerebellar vermis. Computed tomography angiography revealed a hypervascular nodule. These findings were compatible with hemangioblastoma. Thallium-201 single photon emission computed tomography ((201)Tl-SPECT) showed moderately high uptake in the early phase and moderately high retention in the delayed phase, whereas hemangioblastoma shows almost no retention in the delayed phase. The patient underwent total removal of the tumor. The histological diagnosis was clear cell ependymoma (CCE). CCE is a rare subtype of ependymoma, which resembles hemangioblastoma in histological and neuroimaging findings, but is considerably more aggressive. (201)Tl-SPECT can provide useful information for the preoperative differential diagnosis of infratentorial CCE and hemangioblastoma.


Subject(s)
Cerebellar Neoplasms/diagnostic imaging , Cerebellum/diagnostic imaging , Ependymoma/diagnostic imaging , Hemangioblastoma/diagnostic imaging , Thallium Radioisotopes , Tomography, Emission-Computed, Single-Photon/methods , Ataxia/etiology , Cerebellar Neoplasms/pathology , Cerebellar Neoplasms/surgery , Cerebellum/pathology , Cerebellum/surgery , Diagnosis, Differential , Dizziness/etiology , Ependymoma/pathology , Ependymoma/surgery , Hemangioblastoma/pathology , Humans , Male , Middle Aged , Neurosurgical Procedures , Predictive Value of Tests , Prognosis , Treatment Outcome
8.
No Shinkei Geka ; 37(12): 1193-9, 2009 Dec.
Article in Japanese | MEDLINE | ID: mdl-19999551

ABSTRACT

OBJECT: Integration of neuronavigation into brain tumor surgery can improve the accuracy and precision of resection, but most neuronavigation systems require rigid pin fixation of the patient's head throughout the operation. We describe use of a noninvasive skull reference tool, which can replace rigid pin fixation in awake craniotomy and pediatric surgery, when standard pin fixation cannot be used. METHODS AND RESULTS: The skull reference tool (BrainLAB, Munich, Germany) is directly attached to the outer skull with a small self-tapping screw. Virtual scanning of the surface of the face and head achieves patient registration in seconds without requiring the use of fiducial markers or head fixation. This procedure improves patient comfort, cooperativeness, and compliance, resulting in better operating procedures. This skull reference tool is available for children younger than 3 years of age, in whom pin fixing is dangerous. Twelve patients underwent awake surgery and four pediatric patients younger than 3 years old underwent five procedures using this skull reference tool in our hospital between January 2005 and December 2008. The method of utilizing this skull reference tool was easy and sufficiently accurate in these patients. CONCLUSION: The use of this skull reference tool provides an accurate and comfortable method of frameless navigation in patients undergoing awake craniotomy and pediatric patients.


Subject(s)
Neuronavigation/methods , Adult , Brain Neoplasms/surgery , Child, Preschool , Female , Humans , Male , Neuronavigation/instrumentation
9.
Neurol Med Chir (Tokyo) ; 49(11): 549-52, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19940409

ABSTRACT

A 24-year-old man, who had an asymptomatic septum pellucidum cyst incidentally found one year previously, presented with severe headache and right abducens nerve palsy caused by expansion of the midline cyst. Preoperative magnetic resonance (MR) imaging revealed obstructive hydrocephalus due to the enlarged midline cyst. Neuroendoscopic fenestration of the septum pellucidum cyst was successfully performed via a right frontal approach using a high-resolution flexible neuroendoscopic system without complication. Communication between the cyst cavity and bilateral lateral ventricles was constructed via a single trajectory. The entire inner cyst wall could be inspected from the cyst cavity by manipulating the flexible neuroendoscopic system, which excluded the presence of neoplasm. His symptoms were completely relieved after surgery, and postoperative MR imaging showed significant improvement of hydrocephalus and shrinkage of the midline cyst. Septum pellucidum cavum vergae cyst may expand and become symptomatic, so fenestration using a flexible neuroendoscope system may be the optimal method for constructing communication to the bilateral lateral ventricles with minimal invasion.


Subject(s)
Cerebral Ventricle Neoplasms/surgery , Cysts/surgery , Endoscopy/methods , Septum Pellucidum/surgery , Ventriculostomy/instrumentation , Ventriculostomy/methods , Cerebral Ventricle Neoplasms/pathology , Cysts/pathology , Endoscopes/standards , Endoscopes/trends , Humans , Hydrocephalus/pathology , Hydrocephalus/physiopathology , Hydrocephalus/surgery , Lateral Ventricles/pathology , Lateral Ventricles/physiopathology , Lateral Ventricles/surgery , Magnetic Resonance Imaging , Male , Optics and Photonics/instrumentation , Optics and Photonics/methods , Postoperative Complications/etiology , Postoperative Complications/physiopathology , Postoperative Complications/prevention & control , Septum Pellucidum/pathology , Septum Pellucidum/physiopathology , Treatment Outcome , Young Adult
10.
No Shinkei Geka ; 36(8): 693-700, 2008 Aug.
Article in Japanese | MEDLINE | ID: mdl-18700532

ABSTRACT

The negative motor area and anterior and posterior language areas were localized by intraoperative electrical cortical stimulation under the awake condition to evaluate the clinical significance of these areas. Thirty-seven awake craniotomies with language mapping were performed in 36 patients with brain tumors. The negative motor area was determined in 17 cases, and the anterior and posterior language areas were found in 12 and 6 cases, respectively. The negative motor area was located in the precentral gyrus inferior to the orofacial motor area in 16 cases, and in the inferior frontal gyrus anterior to the orofacial motor area in one case. Both the negative motor area and the anterior language area were determined in 8 cases. Anterior language areas in these 8 cases were located anterior and/or inferior to the negative motor areas. The negative motor area is an easily determined, important landmark for intraoperative language mapping.


Subject(s)
Brain Mapping , Brain Neoplasms/physiopathology , Brain Neoplasms/surgery , Cerebral Cortex/physiology , Craniotomy , Language , Motor Cortex/physiology , Wakefulness/physiology , Adult , Aged , Female , Humans , Male , Middle Aged , Monitoring, Intraoperative
11.
Epilepsia ; 43(4): 415-24, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11952773

ABSTRACT

PURPOSE: To investigate the clinical usefulness of magnetoencephalography (MEG) as a guide to the surgical treatment of temporal lobe epilepsy (TLE). METHODS: Preoperative spike localization by MEG was compared with seizure outcome and postoperative spike localization at 12 months after resective surgery in 16 patients with TLE. Spike localization was classified into anterior temporal (AT) and non-AT localization in 11 patients without neocortical lesion treated with anterior temporal lobectomy (ATL); and lesion and lobar localization in five patients with neocortical lesion treated with lesionectomy (n = 3) or lesionectomy with medial temporal resection (n = 2). RESULTS: All five patients with AT localization became seizure free and spike free after surgery. Among the six patients with non-AT localization, two became seizure free and spike free, two became seizure free with residual spikes, one had residual seizures but no spikes, and one had both residual seizures and spikes. All three patients with lesion localization and two with lobar localization had favorable seizure outcome and became spike free after surgery. CONCLUSIONS: MEG spike localization can identify neocortical sources remote from the presumed epileptogenic area. Favorable seizure outcome can be expected in patients with AT localization after ATL and patients with lesion localization after lesionectomy. In contrast, non-AT localization indicates either nonmedial TLE or spike propagation to the posterior and extratemporal neocortex. Similarly, lobar localization indicates spike propagation from an epileptogenic lesion or extensive epileptogenicity. Patients with non-AT localization or lobar localization should undergo intensive evaluations, such as intracranial EEG, for improved seizure outcome.


Subject(s)
Epilepsy, Temporal Lobe/diagnosis , Magnetoencephalography , Action Potentials , Adolescent , Adult , Child , Electroencephalography , Epilepsy, Temporal Lobe/physiopathology , Epilepsy, Temporal Lobe/surgery , Female , Humans , Male , Neocortex/pathology , Postoperative Period , Treatment Outcome
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