1.Differences in Regional Glucose Metabolism of the Brain Measured with F-18-FDG-PET in Patients with Essential Tremor According to Their Response to Beta-Blockers.
In Uk SONG ; Sang Won HA ; Young Soon YANG ; Yong An CHUNG
Korean Journal of Radiology 2015;16(5):967-972
OBJECTIVE: In this study, there was an investigation as to whether there is a functional difference in essential tremor (ET), according to responses to beta-blockers, by evaluating regional changes in cerebral glucose metabolism. MATERIALS AND METHODS: Seventeen male patients with ET were recruited and categorized into two groups: 8 that responded to medical therapy (group A); and 9 that did not respond to medical therapy (group B). Eleven age-sex matched healthy control male subjects were also included in this study. All subjects underwent F-18 fluorodeoxyglucose (FDG)-PET, and evaluated for their severity of tremor symptoms, which were measured as a score on the Fahn-Tolosa-Marin tremor rating scale (FTM). The FDG-PET images were analyzed using a statistical parametric mapping program. RESULTS: The mean FTM score 6 months after the initiation of propranolol therapy was significantly lower in group A (18.13 > 8.13), compared with group B (14.67 = 14.67). The glucose metabolism in group A in the left basal ganglia was seen to be decreased, compared with group B. The ET showed a more significantly decreased glucose metabolism in both the fronto-temporo-occipital lobes, precuneus of right parietal lobe, and both cerebellums compared with the healthy controls. CONCLUSION: Essential tremor is caused by electrophysiological disturbances within the cortical-cerebellar networks and degenerative process of the cerebellum. Furthermore, ET may have different pathophysiologies in terms of the origin of disease according to the response to first-line therapy.
Adrenergic beta-Antagonists/*pharmacology/therapeutic use
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Aged
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Brain/*drug effects/metabolism/radiography
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Brain Mapping
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Essential Tremor/*diagnosis/drug therapy/radiography
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Fluorodeoxyglucose F18/*chemistry
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Glucose/*metabolism
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Humans
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Male
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Middle Aged
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*Positron-Emission Tomography
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Propranolol/pharmacology/therapeutic use
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Radiopharmaceuticals/*chemistry
2.5-Fluorouracil-induced leukoencephalopathy in patients with breast cancer.
Sung Min CHOI ; Seung Han LEE ; Yong Seok YANG ; Byeong Chae KIM ; Myeong Kyu KIM ; Ki Hyun CHO
Journal of Korean Medical Science 2001;16(3):328-334
The purpose of this study is to determine the characteristic clinical features, radiologic findings, and precipitating and prognostic factors in the patients with breast cancer and with 5-Fluorouracil (5-FU)-induced leukoencephalopathy. We reviewed the medical records of six breast cancer patients who developed leukoencephalopathy after chemotherapy which included 5-FU and also evaluated thorough neurological examinations including mini-mental status examination, cerebrospinal fluid studies, brain images and brain biopsies. Six patients exhibited slowly progressing neurologic symptoms characterized by the impairment of cognitive function, abulia, ataxic gait, and/or akinetic mutism. None of the patients had any specific causes or etiologic factors for leukoencephalopathy. Brain MRI in all patients showed diffuse periventricular white matter changes in the T2-weighted MR image. Brain biopsy in Patient 1 showed fragmented axonal fiber and minimally deprived myelination with many scattered macrophages. Five patients who treated with steroids at the onset of neurological symptoms showed clinical improvement, regardless of their age, sex, the pathology and stage of breast cancer, or the total dosage of chemotherapeutic agents. We conclude that leukoencephalopathy in these cases could be attributable to 5-FU neurotoxicity and suggest that the administration of steroids might be the treatment of choice.
Adenocarcinoma, Mucinous/complications/drug therapy
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Adult
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Anti-Inflammatory Agents, Steroidal/therapeutic use
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Antineoplastic Agents/adverse effects/therapeutic use
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Brain/*drug effects/metabolism/radiography
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Breast Neoplasms/*complications/drug therapy
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Carcinoma, Infiltrating Duct/*complications/drug therapy
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Cyclophosphamide/adverse effects/therapeutic use
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Epirubicin/adverse effects/therapeutic use
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Female
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Fluorouracil/*adverse effects/analogs & derivatives/therapeutic use
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Glucocorticoids, Synthetic/therapeutic use
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Human
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Magnetic Resonance Imaging
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Methylprednisolone/therapeutic use
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Middle Age
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Nervous System Diseases/chemically induced/drug therapy/metabolism/radiography
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Prednisolone/therapeutic use
3.Outcome of Postoperative Intratumoral Bleomycin Injection for Cystic Craniopharyngioma.
Dong Hyuk PARK ; Jung Yul PARK ; Joo Han KIM ; Yong Gu CHUNG ; Hoon Kap LEE ; Ki Chan LEE ; Jung Keun SUH
Journal of Korean Medical Science 2002;17(2):254-259
Total excision is a treatment of choice in preventing the relapse of craniopharyn-gioma, but for tumors involving an extensive area, it is often associated with an increased risk of complications. We have performed a partial or subtotal tumor removal followed by repeated injection of bleomycin into the remaining tumor through a subcutaneous reservoir as postoperative adjuvant therapy. A retro-spective review of clinical, radiological, and surgical data was performed for 10 patients (5 males and 5 females; age, 3-65 yr; follow-up duration, 12-79 months) with cystic craniopharyngiomas. The measurements of lactate dehydrogenase (LDH) level at each aspiration were performed. The shrinkage and/or stabiliza-tion of tumor was initially noted in all cases. The recurrence of tumor was seen in 4 cases (40%). The decreased or increased level of LDH was interpreted as tumor shrinkage or recurrence, respectively. The transient toxic reactions were observed in 3 patients (30%). Our study demonstrates that postoperative bleo-mycin injection for cystic craniopharyngioma, although does not appear to eradi-cate the tumor, decreases and stabilizes the tumor size, when used as an adju-vant therapy in young patients.
Adolescent
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Adult
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Aged
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Antibiotics, Antineoplastic/administration & dosage/adverse effects/*therapeutic use
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Bleomycin/administration & dosage/adverse effects/*therapeutic use
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Brain/radiation effects
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Child
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Child, Preschool
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Craniopharyngioma/*drug therapy/radiography/surgery
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Female
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Follow-Up Studies
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Humans
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Injections
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L-Lactate Dehydrogenase/metabolism
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Male
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Middle Aged
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Pituitary Neoplasms/*drug therapy/radiography/surgery
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*Postoperative Care
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Retrospective Studies
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Tomography, X-Ray Computed/methods