1.Percutaneous Selective Radiofrequency Thermocoagulation in the Treatment of Spastic Cerebral Palsy: A case report.
So young LEE ; Jeong seob OH ; Yoon tae JUNG
Journal of the Korean Academy of Rehabilitation Medicine 2008;32(3):340-344
Cerebral palsy is the most common motor disorder in childhood. In cerebral palsy, spasticity can be a very disabling feature: limited locomotor abilities, contracture and gait difficulty. We present two cases of cerebral palsy patients who had treated with oral medication and chemodenervation with the Botulinum toxin A or alcohol but could not walk independently. We performed percutaneous selective radiofrequency thermocoagulation in the tibial motor nerve branch under the general anesthesia. The degree of spasticity, which was measured with modified Ashworth scale and modified Tardieu scale, was reduced and recurrence of the spasticity wasn't seen untill 6 months. Percutaneous selective radiofrequency thermocoagulation could be a treatment option for spasticity of cerebral palsy with little adverse effect.
Anesthesia, General
;
Botulinum Toxins
;
Cerebral Palsy
;
Contracture
;
Electrocoagulation
;
Gait
;
Humans
;
Muscle Spasticity
;
Nerve Block
;
Recurrence
2.Herpes Zoster of Oral and Maxillofacial Area: Cases Report.
Il Kyu KIM ; Jin Ho CHOI ; Sung Rok JEONG ; Seong Seob OH ; Nam Sik OH ; Eui Seong KIM
Journal of the Korean Association of Oral and Maxillofacial Surgeons 2000;26(3):313-317
Herpes zoster is acute viral infection characterized by the appearance of vesicles that occur on the skin and mucous membrane along the pathway of an involved sensory nerve. The incidence is increased in those who have history of trauma, malignant tumor, radiation therapy and the immuno-suppressive drug users. Although herpes zoster is usually as benign viral infection, complications may occur especially when cranial nerves are involved. So careful treatment is necessary when cranial nerves are involved. We have treated two cases. One is involved trigeminal nerve mandibular branch, another maxillary branch. We have used conservative therapy, pain control, acyclovir on this area and obtained good result. After 17 and 8 months respectively, no complications occur in our two cases. So we present two cases with review of literature.
Acyclovir
;
Cranial Nerves
;
Drug Users
;
Herpes Zoster*
;
Humans
;
Incidence
;
Mucous Membrane
;
Skin
;
Trigeminal Nerve
3.Ultrasonographic Findings of Mild and Very Mild Carpal Tunnel Syndrome.
Gi young PARK ; Jung ho BAE ; So young LEE ; Jeong seob OH ; Jeong Geun LIM ; Dae Gu SON
Journal of the Korean Academy of Rehabilitation Medicine 2008;32(1):67-72
OBJECTIVE: To assess the clinical usefulness of ultrasonography for the diagnosis of mild and very mild carpal tunnel syndrome. METHOD: Ultrasonographic evaluation was performed in 39 hands of 29 patients with mild and very mild carpal tunnel syndrome according to Bland's neurophysiologic grading scale. Controls included 41 hands of 34 subjects without electrophysiologic evidence of carpal tunnel syndrome. Ultrasonographic findings were evaluated quantitatively with regard to the cross-sectional area, the flattening ratio, the swelling ratio of the median nerve, and palmar displacement of the flexor retinaculum. The analysis of differences between controls and patients group were done by independent t-test. Cut-off values using receiver operation characteristic, were calculated. RESULTS: Patients had significantly increased cross sectional area and flattening ratio of the median nerve at proximal carpal area, palmar displacement of the flexor retinaculum at proximal carpal area. A critical value of equal or higher to 8.5 mm(2) for cross-sectional area at the pisiform level showed a sensitivity 79.5%, a specificity of 95.1%, which had most diagnostic value compared with the value of cross-sectional area at the distal radius level, flattening ratio at the pisiform level and palmar displacement. CONCLUSION: Ultrasonography was useful in the diagnosis of mild and very mild carpal tunnel syndrome.
Carpal Tunnel Syndrome
;
Displacement (Psychology)
;
Hand
;
Humans
;
Median Nerve
;
Radius
;
Sensitivity and Specificity
4.Antidepressant Effects of Mirtazapine in Patients with Major Depression.
Hong Shick LEE ; Ho Suk SUH ; Chan Hyung KIM ; Kwang Soo KIM ; Jeong Ho CHAE ; Kang Seob OH
Korean Journal of Psychopharmacology 2000;11(2):126-135
OBJECTIVES: Mirtazapine is a newly introduced antidepressant in Korea. The purpose of this study is to evaluate effectiveness and safety of mirtazapine as an antidepressant for the first time in Korean patients with major depression. METHODS: This study is an open, non-comparative, multicenter study treated with mirtazapine for 6 weeks in patients with DSM-IV diagnosis of major depression who have 17-item HAMD score> or = 18 and who are between 18 and 65 years of age. Mirtazapine was administered 30 mg orally as an initial dose and could be increased to 45 mg from the 14th day of treatment, depending on the therapeutic responses of subjects. The clinical efficacy of mirtazapine was assessed at the baseline and at the 1st, 2nd, 4th, and 6th week of treatment. To assess the clinical efficacy of the drug, well-trained psychiatrists have evaluated subjects using 17-item HAMD and CGI on each evaluation periods. Also, for the evaluation of subjective symptoms of patients, BDI was used. Adverse experiences associated with mirtazapine were evaluated on each visit, with recordings of blood pressure, heart rate and weight. The responders were defined as patients with > or = 50% decrease from baseline in total 17-item HAMD scores and remitted patients with a total 17-item HAMD score of < or = 7. RESULTS: Out of 79 subjects enrolled, 45 were completed this study. After 6 weeks, the score of 17-item HAMD, CGI and BDI demonstrated statistically significant decrease compared with at the baseline. This decrease was observed as early as the 1st week of mirtazapine treatment. Moreover, the meaningful reduction in each total scores of these different parameters on each evaluation period could be detected, except in case of 2-4 week and 4-6 week of BDI. The responder rate was 15.6% at the first week of mirtazapine treatment, 88.9% at the 6th week. The rate of remission was 2.2% at the first week and 60.0% at the 6th week. The most frequent adverse events during 6 weeks were somnolence(31.6%), drowsiness(19%) and weight gain(17.7%). Aside from sedation and weight gain, anticholinergic, cardiovascular and stimulating side effects are less than 10%, and no one complained about sexual dysfunction. The dropouts(34 subjects, 43%) were caused by adverse events(38.2%), insufficient compliance(35.3%) and uncooperation with the study(20.6%). CONCLUSION: Mirtazapine has shown to have superior antidepressant effect in this study. Especially, this effect appeared from the early treatment phase, the 1st week of treatment. The most frequent adverse events reported were somnolence, drowsiness and weight gain. Anticholinergic, cardiovascular, stimulating adverse events as well as sexual dysfunction were rarely reported, and there was no clinical significant change on physical examinations. Therefore this study showed that mirtazapine is a superior and safe antidepressant in patients with major depression.
Blood Pressure
;
Depression*
;
Diagnosis
;
Diagnostic and Statistical Manual of Mental Disorders
;
Heart Rate
;
Humans
;
Korea
;
Physical Examination
;
Psychiatry
;
Sleep Stages
;
Weight Gain
5.Antidepressant Effects of Mirtazapine in Patients with Major Depression.
Hong Shick LEE ; Ho Suk SUH ; Chan Hyung KIM ; Kwang Soo KIM ; Jeong Ho CHAE ; Kang Seob OH
Korean Journal of Psychopharmacology 2000;11(2):126-135
OBJECTIVES: Mirtazapine is a newly introduced antidepressant in Korea. The purpose of this study is to evaluate effectiveness and safety of mirtazapine as an antidepressant for the first time in Korean patients with major depression. METHODS: This study is an open, non-comparative, multicenter study treated with mirtazapine for 6 weeks in patients with DSM-IV diagnosis of major depression who have 17-item HAMD score> or = 18 and who are between 18 and 65 years of age. Mirtazapine was administered 30 mg orally as an initial dose and could be increased to 45 mg from the 14th day of treatment, depending on the therapeutic responses of subjects. The clinical efficacy of mirtazapine was assessed at the baseline and at the 1st, 2nd, 4th, and 6th week of treatment. To assess the clinical efficacy of the drug, well-trained psychiatrists have evaluated subjects using 17-item HAMD and CGI on each evaluation periods. Also, for the evaluation of subjective symptoms of patients, BDI was used. Adverse experiences associated with mirtazapine were evaluated on each visit, with recordings of blood pressure, heart rate and weight. The responders were defined as patients with > or = 50% decrease from baseline in total 17-item HAMD scores and remitted patients with a total 17-item HAMD score of < or = 7. RESULTS: Out of 79 subjects enrolled, 45 were completed this study. After 6 weeks, the score of 17-item HAMD, CGI and BDI demonstrated statistically significant decrease compared with at the baseline. This decrease was observed as early as the 1st week of mirtazapine treatment. Moreover, the meaningful reduction in each total scores of these different parameters on each evaluation period could be detected, except in case of 2-4 week and 4-6 week of BDI. The responder rate was 15.6% at the first week of mirtazapine treatment, 88.9% at the 6th week. The rate of remission was 2.2% at the first week and 60.0% at the 6th week. The most frequent adverse events during 6 weeks were somnolence(31.6%), drowsiness(19%) and weight gain(17.7%). Aside from sedation and weight gain, anticholinergic, cardiovascular and stimulating side effects are less than 10%, and no one complained about sexual dysfunction. The dropouts(34 subjects, 43%) were caused by adverse events(38.2%), insufficient compliance(35.3%) and uncooperation with the study(20.6%). CONCLUSION: Mirtazapine has shown to have superior antidepressant effect in this study. Especially, this effect appeared from the early treatment phase, the 1st week of treatment. The most frequent adverse events reported were somnolence, drowsiness and weight gain. Anticholinergic, cardiovascular, stimulating adverse events as well as sexual dysfunction were rarely reported, and there was no clinical significant change on physical examinations. Therefore this study showed that mirtazapine is a superior and safe antidepressant in patients with major depression.
Blood Pressure
;
Depression*
;
Diagnosis
;
Diagnostic and Statistical Manual of Mental Disorders
;
Heart Rate
;
Humans
;
Korea
;
Physical Examination
;
Psychiatry
;
Sleep Stages
;
Weight Gain
6.The Effect of Percutaneous Selective Radiofrequency Thermocoagulation in the Treatment of Spasticity with Cerebral Palsy.
So Young LEE ; Jeong Seob OH ; Yoon Tae JUNG ; Kyung Sik CHOI
Journal of the Korean Academy of Rehabilitation Medicine 2009;33(2):198-204
OBJECTIVE: To compare the therapeutic effects between radiofrequency thermocoagulation and phenol motor branch block in treatment of spasticity of child with cerebral palsy. METHOD: Thirteen patients with spastic cerebral palsy were randomly divided into two groups. One group received percutaneous selective radiofrequency thermocoagulation on tibial nerve motor branch and the other group received phenol motor branch block to the gastrocnemius muscle. Therapeutic effects were assessed before and after treatment for 6 months in each group. The severity of ankle spasticity was assessed with the modified Ashworth scale (MAS), the modified Tardieu scale (MTS), and the passive range of motion (PROM) of ankle joint. RESULTS: In both groups, the MAS and MTS decreased, and radiofrequency thermocoagulation group showed more significant reduction of the spasticity (p<0.05). There was a significant increase in PROM on knee flexion and extension in a radiofrequency thermocoagulation group (p<0.05). CONCLUSION: Percutaneous selective radiofrequency thermocoagulation could be a treatment option for relieving the localized spasticity of ankle in spastic cerebral palsy with little adverse effect.
Animals
;
Ankle
;
Ankle Joint
;
Cerebral Palsy
;
Child
;
Electrocoagulation
;
Humans
;
Knee
;
Muscle Spasticity
;
Muscle, Skeletal
;
Phenol
;
Range of Motion, Articular
;
Tibial Nerve
7.Fetal vesico-amniotic shunting procedure (VASP) for posterior urethral valve syndrome at 19weeks' gestation.
Jeong Hoon RHO ; Mi Hye PARK ; Jin Seob LIM ; Joong Gyu HA ; Kwan Young OH ; Yun Seok YANG ; In Taek HWANG ; Ji Hak JEONG ; Jun Sook PARK
Korean Journal of Obstetrics and Gynecology 2001;44(11):2122-2126
An ultrasonographic examination revealed increased fetal bladder size and decreased AFI as well as fetal bilateral hydronephrosis at 173weeks' gestation. Diagnosis of the fetal posterior urethral valve syndrome was made. Percutaneous fetal bladder puncture with aspiration and amniocentesis was performed. The fetus was normal male karyotype and with a predicted good renal function(sodium concentration, chloride concentration, and osmolarity at 74 mEq/L, 60 mEq/L, and 148 mOsm, respectively). So, the fetus underwent amnioinfusion and vesico-amniotic shunting procedure (VASP) using a double-basket catheter at 194weeks' gestation in order to prevent development of dysplastic kidneys and hypoplastic lungs. The healthy male baby was delivered at 384weeks' gestation and had normally functioning kidney. Cutaneous vesicostomy was performed for the newborn since the urethral orifice was small. The one year old infant is now well and waiting for urethroscopic valve ablation procedure.
Amniocentesis
;
Catheters
;
Cystostomy
;
Diagnosis
;
Fetus
;
Humans
;
Hydronephrosis
;
Infant
;
Infant, Newborn
;
Karyotype
;
Kidney
;
Lung
;
Male
;
Osmolar Concentration
;
Pregnancy*
;
Punctures
;
Urinary Bladder
8.Sepsis Developed from an Odontogenic Infection: Case Report
Moon Seob KIM ; Su Gwan KIM ; Seong Yong MOON ; Ji Su OH ; Jin Ju PARK ; Mi Ae JEONG ; Seok Jin YANG ; Jong Won JUNG ; Jeong Sun KIM
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons 2011;33(5):445-448
9.A Case of Infiltrating Lipoma Combined with Nevus Lipomatosus Cutaneous Superficialis.
Seung Il KIM ; Moon Cheol JEONG ; Jae Hak YOO ; Kea Jeung KIM ; Joo Seob KEUM ; Tae Yoon OH
Korean Journal of Dermatology 1999;37(10):1491-1494
Infiltrating lipoma is one of the most deep-seated benign soft tissue tumor which occupies less than 1% in lipomas. There are two different types of infiltrating lipoma, one intramuscular lipoma, and the other intermuscular lipoma. Nevus lipomatosus cutaneous superficialis is a very rare skin disease which is characterized by the ectopic presence of mature adipose tissue in the dermis. In this disease two clinical types are distinguished: The first classic type is the multiple lesions of zonal distribution usually on the buttocks or on the lower back area. The second type is the solitary papule or nodule with less restricted tendency in its distrubution. We described a 31-year-old man who had a relatively well-defined localized, skin colored, 20x20cm sized, subcutaneous mass partially covered with brown colored papules and plaque on the left subscapular area. The skin lesion began about 11 years ago with brown colored papules and gradually increased in size to 20x20cm mass. Histopathological and clinical findings showed ectopic fat lobules consisted of almost mature cells in the dermis, between the each muscle fibers, and each muscle bundles.
Adipose Tissue
;
Adult
;
Buttocks
;
Dermis
;
Fluconazole
;
Humans
;
Lipoma*
;
Nevus*
;
Skin
;
Skin Diseases
10.Reduction of Postischemic Cerebral Infarction and Cerebral Edema by Superoxide Dismutase and Allopurinol.
Woo Seok OH ; Yun Kwan PARK ; Yong Ku CHONG ; Heung Seob CHUNG ; Jung Keun SUH ; Hoon Kap LEE ; Jeong Wha CHU ; Ki Chan LEE
Journal of Korean Neurosurgical Society 1991;20(4):218-223
The authors have inverstigated the hypothesis that ischemic injury could be attenuated by xanthine oxidase inhibitor(Allopurinol) and superoxide dismutase(SOD). This study used rat MAC model. Each animal was assigned to four groups which was composed with control group, allopurinol pretreated group(50mg/kg. I.P single). SOD pretreated group(16,000 I.U/kg I.V q 15min for 4hours) and combined pretreatment group. Oxygen derived free radicals have been implicated in various pathological conditions including ischemia. Xanthine oxidase serve as a source of oxidizing agents such as superoxide radical and hydrogen peroxide. The superoxide flux in normal cells appears to have necessitated the development of SOD, which scavenges the superoxide by dismutation. Infarcted area was measured by computerized morphometric analysis after triphenyl tetrazolium chloride staining, infarcted area was reduced in SOD treated group(p=0.005) and SOD, allopurinol combined group(P=0.035). Brain edema was measured by gravimetric method. And it was reduced in Allopurinol treated group(P=0.001) and SOD allopurinol combined group (P<0.001). Thus it was revealed that ischemic injury might be reduced by either decrease of production or increase of scavenger and the combination of two should be more efficious.
Allopurinol*
;
Animals
;
Brain Edema*
;
Cerebral Infarction*
;
Free Radicals
;
Hydrogen Peroxide
;
Ischemia
;
Oxidants
;
Oxygen
;
Rats
;
Superoxide Dismutase*
;
Superoxides*
;
Xanthine Oxidase