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1.
Anesthesia and Pain Medicine ; : 382-386, 2021.
Artigo em Inglês | WPRIM | ID: wpr-913377

RESUMO

Background@#Gasserian ganglion radiofreqeucy thermoablation is a good treatment option for the management of pain in trigeminal neuralgia. We report a case in which the patient of trigeminal neuralgia combined with anterior cerebral artery aneurysm was treated successfully by gasserian ganglion thermoablation without any complication.CaseAn 85-year-old female presenting with electric shock like sensation in the gum and molar teeth was diagnosed as trigeminal neuralgia. Carbamazepine medication and trigeminal nerve blockade relieved her pain partially, but severe side effects of carbamazepine occurred. Magnetic resonance angiography of the brain showed saccular aneurysm in inferior aspect of the anterior communicating artery. Gasserian ganglion thermoablation under sedation anesthesia using nicardipine was performed carefully without any rupture of the cerebral aneurysm. @*Conclusions@#Gasserian ganglion thermoablation could be performed safely in a patient with cerebral aneurysm without any inadvertent event.

2.
The Korean Journal of Parasitology ; : 677-680, 2014.
Artigo em Inglês | WPRIM | ID: wpr-124055

RESUMO

Infection cases of diphyllobothriid tapeworms are not much in the below teen-age group. We report a case of Diphyllobothrium nihonkaiense infection in a 13-year-old boy. He presented with severe fatigue, occasional abdominal pain at night time. He also had several episodes of tapeworm segment discharge in his stools. By his past history, he had frequently eaten raw fish including salmon and trout with his families. Numerous eggs of diphyllobothriid tapeworm were detected in the fecal examination. We introduced amidotrizoic acid as a cathartic agent through nasogastroduodenal tube and let nearly whole length (4.75 m) of D. nihonkaiense be excreted through his anus. After a single dose of praziquantel, the child's stool showed no further eggs, and his symptoms disappeared. The evacuated worm was identified as D. nihonkaiense by mitochondrial cox1 gene analysis. Here we report a successful extracorporeal worm extraction from an infection case of D. nihonkaiense by the injection of amidotrizoic acid.


Assuntos
Adolescente , Animais , Humanos , Masculino , Antiparasitários/uso terapêutico , Ciclo-Oxigenase 1/genética , Diatrizoato de Meglumina/uso terapêutico , Difilobotríase/tratamento farmacológico , Diphyllobothrium/classificação , Fezes/parasitologia , Praziquantel/uso terapêutico , Análise de Sequência de DNA
3.
Korean Journal of Psychopharmacology ; : 199-207, 2011.
Artigo em Coreano | WPRIM | ID: wpr-116547

RESUMO

OBJECTIVE: This study was aimed to identify the correlation between antipsychotics-induced amenorrhea, and attitudes toward treatment and quality of life in women with schizophrenia. METHODS: Twenty female schizophrenic patients with antipsychotics-induced amenorrhea and thirty female schizophrenic patients without antipsychotics-induced amenorrhea were evaluated. Attitudes toward treatment were assessed by the Korean version of Drug Attitude Inventory (KDAI-10) and quality of life was assessed by the Korean version of World Health Organization Quality of Life Assessment Instrument-BREF (WHOQOL-BREF). The psychopathology of each patient was assessed by the Positive and Negative Syndrome Scales and the Clinical Global Impression-Severity. Adverse effects were evaluated using the Drug-Induced Extrapyramidal Symptoms Scale. Correlation analysis and multiple linear regression were conducted. RESULTS: The KDAI-10 score was not significantly correlated antipsychotics-induced amenorrhea. In WHOQOL-BREF score, social relation domain only showed significant correlation with antipsychotics-induced amenorrhea. Multiple linear regression analysis revealed that the number of family members contributed significantly to the Positive Subjective Feelings Scores of KDAI-10 and marital status contributed significantly to the social relation domain of WHOQOL-BREF in amenorrhea group. CONCLUSION: The results of present study suggest that antipsychotics-induced amenorrhea lower part of the quality of life domain in women with schizophrenia. Clinicians must pay attention to treatment of amenorrhea and various factors that correlated with attitudes toward treatment and quality of life in women with schizophrenia.


Assuntos
Feminino , Humanos , Amenorreia , Modelos Lineares , Estado Civil , Psicopatologia , Qualidade de Vida , Esquizofrenia , Pesos e Medidas , Organização Mundial da Saúde
4.
Journal of the Korean Child Neurology Society ; (4): 66-73, 2010.
Artigo em Coreano | WPRIM | ID: wpr-208705

RESUMO

PURPOSE: Sleep is correlated with various neurological disorders. Epilepsy and chronic headaches(CH) are the most common causes of visiting children in neurology clinics. The aim of the present study is to evaluate the sleeping patterns of patients with epilepsy and CH. METHODS: Children and adolescents of between the ages 6-18 suffering from epilepsy or CH were assessed using the sleep questionnaires. Patients with motor disabilities, chromosomal abnormalities or neuromuscular diseases were excluded. RESULTS: Sleeping patterns of the 276 patients were analyzed(200 epilepsy and 76 CH). The mean age of the patients was 11.8+/-3.3 years. CH patients had more excessive daytime sleepiness, shorter total sleep time on weekday, later bedtime, and more trouble getting up in the morning than epilepsy patients(P<0.001). CH patients also had more mood instabilities, resistance to going to bed on time, and uncomfortable feelings in legs than epilepsy patients(P<0.05). On the contrary, epilepsy patients had more bed-wettings than CH patients(P<0.05). CONCLUSION: It is suggested that CH is more associated with sleep problems than epilepsy. The consideration and proper treatment for accompanying sleep problems are needed when we treat chronic headaches or epilepsy.


Assuntos
Adolescente , Criança , Humanos , Aberrações Cromossômicas , Epilepsia , Cefaleia , Transtornos da Cefaleia , Perna (Membro) , Doenças do Sistema Nervoso , Neurologia , Doenças Neuromusculares , Inquéritos e Questionários , Estresse Psicológico
5.
The Journal of the Korean Society for Therapeutic Radiology and Oncology ; : 147-154, 2010.
Artigo em Inglês | WPRIM | ID: wpr-180478

RESUMO

PURPOSE: To investigate the radiosensitizing effect of the selective epidermal growth factor receptor (EGFR) inhibitor nimotuzumab in human colorectal cancer cell lines. MATERIALS AND METHODS: Four human colorectal cancer cell lines, HCT-8, LoVo, WiDr, and HCT-116 were treated with nimotuzumab and/or radiation. The effects on cell proliferation, viability, and cell cycle progression were measured by MTT, clonogenic survival assay, flow cytometry, and Western blot. RESULTS: An immunoblot analysis revealed that EGFR phosphorylation was inhibited by nimotuzumab in colorectal cancer cell lines. Under these experimental conditions, pre-treatment with nimotuzumab increased radiosensitivity of colorectal cancer cell lines, except for cell line HCT-116. However, cell proliferation or cell cycle progression was not affected by the addition of nimotuzumab, irrespective of irradiation. CONCLUSION: Nimotuzumab enhanced the radiosensitivity of colorectal cancer cells in vitro by inhibiting EGFR-mediated cell survival signaling. This study provided a rationale for the clinical application of the selective EGFR inhibitor, nimotuzumab in combination with radiation in colorectal cancer cells.


Assuntos
Humanos , Anticorpos Monoclonais Humanizados , Western Blotting , Ciclo Celular , Linhagem Celular , Proliferação de Células , Sobrevivência Celular , Neoplasias Colorretais , Citometria de Fluxo , Fosforilação , Tolerância a Radiação , Radiossensibilizantes , Receptores ErbB
6.
Korean Journal of Pediatrics ; : 824-831, 2009.
Artigo em Coreano | WPRIM | ID: wpr-175063

RESUMO

PURPOSE: We aimed to investigate the efficacy of and functional recovery after intracerebral transplantation of different doses of mouse mesenchymal stem cells (mMSCs) in immature rat brain with hypoxic-ischemic encephalopathy (HIE). METHODS: Postnatal 7-days-old Sprague-Dawley rats, which had undergone unilateral HI operation, were given stereotaxic intracerebral injections of either vehicle or mMSCs and then tested for locomotory activity in the 2nd, 4th, 6th, and 8th week of the stem cell injection. In the 8th week, Morris water maze test was performed to evaluate the learning and memory dysfunction for a week. RESULTS: In the open field test, no differences were observed in the total distance/the total duration (F=0.412, P=0.745) among the 4 study groups. In the invisible-platform Morris water maze test, significant differences were observed in escape latency (F=380.319, P<0.01) among the 4 groups. The escape latency in the control group significantly differed from that in the high-dose mMSC and/or sham group on training days 2-5 (Scheffe's test, P<0.05) and became prominent with time progression (F=6.034, P<0.01). In spatial probe trial and visible-platform Morris water maze test, no significant improvement was observed in the rats that had undergone transplantation. CONCLUSION: Although the rats that received a high dose of mMSCs showed significant recovery in the learning-related behavioral test only, our data support that mMSCs may be used as a valuable source to improve outcome in HIE. Further study is necessary to identify the optimal dose that shows maximal efficacy for HIE treatment.


Assuntos
Animais , Humanos , Recém-Nascido , Camundongos , Ratos , Encéfalo , Lesões Encefálicas , Isquemia Encefálica , Hipóxia-Isquemia Encefálica , Aprendizagem , Memória , Células-Tronco Mesenquimais , Metionina , Ratos Sprague-Dawley , Salicilamidas , Células-Tronco , Compostos de Sulfônio , Transplantes , Nações Unidas
7.
Korean Journal of Pediatrics ; : 162-169, 2008.
Artigo em Coreano | WPRIM | ID: wpr-218627

RESUMO

PURPOSE: Oxcabarzepine (OXC), newly recommended antiepileptic drug, has been prescribed for patients with partial seizures and generalized tonic clonic seizures in Korea from 1999. There are limited reports about an efficacy of OXC therapy in epileptic children in Korea. This study evaluated the efficacy and safety of OXC in the light of our experience. METHODS: The patients, who had visited the pediatric neurology clinic of Korea University Guro Hospital from January 2001 to December 2006, were included. The data of 144 patients who were administrated OXC as monotherapy or polytherapy, was summarized retrospectively and we evaluated the efficacy and safety of OXC. RESULTS: After 6 months of OXC therapy, 77 patients (53.5%, n=144) achieved seizure freedom, 48 patients (33.3%) experienced >50% improvement. After 12 months of OXC therapy, cessation of seizure was observed in 88 patients (61.1%, n=133), and 27 patients (18.8%) manifested an improvement. Monotherapy group showed superior efficacy to polytherapy one. The frequent side effects of OXC were drowsiness (20.1%), headache (12.5%), dizziness (9.7%) and rash (8.3%). They did not related to patient's age or sex, and dosage of OXC. Twenty four patients (16.7%) experienced hyponatremia, but which were neither symptomatic nor significant one. CONCLUSION: The efficacy and safety of OXC in our patients were excellent and had less significant side effects than established international one. We expect this report contributes toward OXC therapy in epileptic children.


Assuntos
Criança , Humanos , Carbamazepina , Tontura , Exantema , Liberdade , Cefaleia , Hiponatremia , Coreia (Geográfico) , Luz , Neurologia , Estudos Retrospectivos , Convulsões , Fases do Sono
8.
The Journal of the Korean Society for Therapeutic Radiology and Oncology ; : 166-172, 2008.
Artigo em Coreano | WPRIM | ID: wpr-154636

RESUMO

PURPOSE: The measurement of radiosensitivity of individuals is useful in radiation therapy. Unfortunately, the measurement of radiation survival using a clonogenic assay, which is the established standard, can be difficult and time consuming. The aim of this study is to compare radiosensitivity results obtained from the MTT and clonogenic assays, and to evaluate whether the MTT assay can be used on clinical specimens. MATERIALS AND METHODS: HCT-8, LoVo, CT-26, and WiDr were the colon cancer cell lines used for this study. The clonogenic assay was performed to obtain the cell survival curves and surviving fractions at a dose of 2 Gy (SF2) as the standard technique for radiosensitivity. Also, the MTT assay was performed for each of the cell lines (in vitro). To simulate clinical specimens, the cell lines were inoculated into nude mice, removed when the tumors reached 1 cm in diameter, and chopped. Next, the tumors were subjected to the same process involved with the MTT assay in vitro. The inhibition rates (IR) of 10 Gy or 20 Gy of irradiation for in vitro and ex vivo were calculated based on the optical density of the MTT assay, respectively. RESULTS: According to SF2 and the cell survival curve, the HCT-8 and WiDr cell lines were more resistant to radiation than LoVo and CT-26 (p<0.05). The IR was measured by in vitro. The MTT assay IR was 17.3%, 21%, 30% and 56.5% for the WiDr, HCT-8, LoVo and CT-26 cell lines, respectively. In addition, the IR measured ex vivo by the MTT assay was 23.5%, 26%, 38% and 53% in the HCT-8, WiDr, LoVo and CT-26 tumors, respectively. CONCLUSION: The radiosensitivity measured by the MTT assay was correlated with the measures obtained from the clonogenic assay. This result highlights the possibility that the MTT assay could be used in clinical specimens for individual radiosensitivity assays.

9.
Journal of the Korean Society of Pediatric Nephrology ; : 100-105, 2007.
Artigo em Coreano | WPRIM | ID: wpr-220792

RESUMO

Cockayne syndrome is a rare autosomal recessive disorder characterized by cachectic dwarfism, mental retardation, loss of facial subcutaneous adipose tissue, microcephaly and photosensitive dermatitis. It is associated with renal abnormalities characterized by hyalinization of glomeruli, atrophy of tubules and interstitial fibrosis. To our knowledge, this is the first report of a case of Cockayne syndrome with FSGS in Korea. A 7-year old boy was admitted for evaluation of hypertension and proteinuria, which were detected 2 month ago. He was followed for short stature(<3 percentile), mental retardation(IQ 55), strabismus and dental caries since 3 years ago. He also showed microcephaly, a bird-like face and relatively large hands and feet. Laboratory findings showed decreased creatinine clearance(CCr 76.1 mL/min/1.73m2) and proteinuria(1,548 mg/day). Renal biopsy demonstrated focal segmental glomerulosclerosis of the hilar type with large hyaline deposits, moderate tubular atrophy and interstitial fibrosis. His cardinal features, mental retardation, and renal biopsy findings were consistent with Cockayne syndrome. We report here a very rare case of Cockayne syndrome with FSGS presenting with proteinuria and hypertension.


Assuntos
Criança , Humanos , Masculino , Atrofia , Biópsia , Síndrome de Cockayne , Creatinina , Cárie Dentária , Dermatite , Nanismo , Fibrose , , Glomerulosclerose Segmentar e Focal , Mãos , Hialina , Hipertensão , Deficiência Intelectual , Coreia (Geográfico) , Microcefalia , Proteinúria , Estrabismo , Gordura Subcutânea
10.
Journal of the Korean Society of Pediatric Nephrology ; : 106-111, 2007.
Artigo em Coreano | WPRIM | ID: wpr-220791

RESUMO

Henoch-Schonlein Purpura(HSP) is a form of vasculitis that typically affects small arteries in the skin, joints, intestinal tract and kidneys. It usually resolves spontaneously but sometimes can cause serious problems in the kidneys and intestinal tract. A 6-year-old girl with purpura, arthralgia and abdominal pain for 2 weeks was admitted. She also showed gross hematuria, generalized edema and decreased urine output. Blood pressure was in the upper normal range. Initial laboratory findings showed hypoalbuminemia, hyperlipidemia, microhematuria and nephrotic-range proteinuria(27.2 g/day). Initially, she was treated with pulse methylprednisolone, azathioprine, albumin and furosemide. Her renal biopsy revealed diffuse mesangial proliferation with strong IgA deposition. There were no crescents. On the third hospital day, she complained of severe abdominal pain and free peritoneal air was seen on abdominal X-ray. Primary repair of small bowel was performed and two pin-point sized holes were found. One week later, she still showed heavy proteinuria. Therefore, we added an ACE inhibitor and dipyridamole, and changed azathioprine to cyclosporine. One month later, the urine protein/creatinine ratio was decreased to 17.8 from 57, but heavy proteinuria has been still persisted. Here we report a rare case of a patient with HSP who had both severe nephrritc-nephrotic syndrome and small bowel perforation.


Assuntos
Criança , Feminino , Humanos , Dor Abdominal , Artérias , Artralgia , Azatioprina , Biópsia , Pressão Sanguínea , Ciclosporina , Dipiridamol , Edema , Furosemida , Hematúria , Hiperlipidemias , Hipoalbuminemia , Imunoglobulina A , Perfuração Intestinal , Articulações , Rim , Metilprednisolona , Nefrite , Proteinúria , Púrpura , Vasculite por IgA , Valores de Referência , Pele , Vasculite
11.
Korean Journal of Pediatrics ; : 278-286, 2006.
Artigo em Coreano | WPRIM | ID: wpr-96050

RESUMO

PURPOSE: Although suprapubic bladder aspiration(SBA) is the most reliable technique for identifying bacteriuria in young infant, no report has been published about the clinical manifestations of urinary tract infection(UTI) diagnosed by aspirated urine in Korea. This study was performed to examine clinical manifestations and related factors of UTI confirmed by a positive urine culture obtained by SBA in young infants. METHODS: We reviewed medical records of 159 infants younger than six months of age, who had been admitted for UTI to Korea University Ansan Hospital from January 2002 to June 2005. RESULTS: The male:female ratio was 5.1:1. The most common pathogen in urine culture was Escherichia coli(92.5 percent). Most of the gram-negative pathogens had high sensitivity to amikacin, or third generation cephalosporins and had low sensitivity to ampicillin, trimethoprim-sulfamethoxazole, or gentamicin. Hydronephrosis and vesicoureteral reflux(VUR) were present in 32.7 percent and 27.7 percent respectively. Renal cortical defects observed on DMSA scans were detected in 37.1 percent. Prolonged fever duration and hospital day, high erythrocyte sedimentation rate(ESR) and C-reactive protein(CRP) levels, hydronephrosis and VUR were related to the renal cortical defects(P<0.05). Rates of UTI-associated bacteremia and aseptic meningitis were 8.3 percent and 6.6 percent. CONCLUSION: Early differential diagnosis is very important in infants younger than 6 months of age with UTI because the clinical findings are non-specific and UTI-associated bacteremia and aseptic meningitis are concomitantly found. Because prolonged fever and higher ESR and CRP levels are risk factors of the renal cortical defects, radiologic evaluations and nephrologic follow-up were needed in identifying the predisposing congenital abnormalities and chronic renal scarring.


Assuntos
Humanos , Lactente , Amicacina , Ampicilina , Bacteriemia , Bacteriúria , Sedimentação Sanguínea , Cefalosporinas , Cicatriz , Anormalidades Congênitas , Diagnóstico Diferencial , Escherichia , Febre , Gentamicinas , Hidronefrose , Coreia (Geográfico) , Prontuários Médicos , Meningite , Meningite Asséptica , Pielonefrite , Fatores de Risco , Succímero , Combinação Trimetoprima e Sulfametoxazol , Bexiga Urinária , Infecções Urinárias , Sistema Urinário
12.
Journal of the Korean Pediatric Society ; : 561-565, 2003.
Artigo em Coreano | WPRIM | ID: wpr-97504

RESUMO

PURPOSE: Urinary tract infection(UTI) is the most common bacterial infectious disease that may induce severe renal injury unless early diagnosis and appropriate treatment are performed. If recurrent UTI is prevented, renal injury can be also reduced. Therefore, we studied the risk factors of recurrent UTI in children. METHODS: We performed a retrospective study of 168 children(58 girls and 110 boys) who were treated for UTI in the Department of Pediatrics, Korea University Medical Center, during 2000-2001. Among 168 children, 93 children were followed up for more than six months. For the detection of recurrence of UTI, we performed monthly routine urine cultures and physical examinations. RESULTS: The total rate of recurrence was 32.3%. The recurrent rate in boys and girls were 37.1% and 17.4%, respectively(P<0.05). The most common causative bacteria in the first onset and in recurrence were Escherichia coli. There was a significant difference in the onset age of UTI between boys with recurrence(4.8+/-1.0 months) and without recurrence(16.5+/-3.8 months)(P<0.01). In 77% of cases, urinary tract infection recurred within six months of the first infection. The time of the first recurrence after UTI was 3.7+/-0.6 months in boys and 14+/-8.2 months in girls(P<0.01). The number of recurrences showed a significant difference between the group under the age of one year(0.69+/-0.8/year) and those above the age of one year(0.16+/-0.4/year)(P<0.05). There was no difference in the recurrent rate between those with structural abnormality and those with normal anatomy. CONCLUSION: Monthly routine urine cultures are efficient in detecting recurrent UTI in children. Because the male sex and young age especially less than one year of age are risk factors for increased recurrence rate of UTI, these children should be followed-up with urine cultures.


Assuntos
Criança , Feminino , Humanos , Masculino , Centros Médicos Acadêmicos , Idade de Início , Bactérias , Doenças Transmissíveis , Diagnóstico Precoce , Escherichia coli , Seguimentos , Coreia (Geográfico) , Pediatria , Exame Físico , Recidiva , Estudos Retrospectivos , Fatores de Risco , Infecções Urinárias , Sistema Urinário
13.
Journal of the Korean Society of Pediatric Nephrology ; : 266-273, 2002.
Artigo em Coreano | WPRIM | ID: wpr-85591

RESUMO

There are several diseases characterized by neurologic abnormalities and renal disease. Joubert syndrome is one of them. Joubert syndrome is a relatively rare autosomal recessive syndrome. The most significant and constant neurologic finding is hypoplasia of the cerebellar vermis. Joubert syndrome is associated with hypotonia, retinal dystrophy, abnormal eye movement, delayed development, abnormal respiratory pattern (neonatal episodic tachypnea or apnea) and nephronophthisis. We report a boy with Joubert syndrome associated with nephrocalcinosis and agenesis of the cerebellar vermis. This patient had also abnormal eye movement, hypotonia, abnormal respiratory pattern, delayed development and chronic renal failure.


Assuntos
Humanos , Masculino , Movimentos Oculares , Falência Renal Crônica , Hipotonia Muscular , Nefrocalcinose , Manifestações Neurológicas , Distrofias Retinianas , Taquipneia
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