1.Diagnostic p53 expression in gastric endoscopic mucosal resection.
Jeong Hee CHO ; Im Hwan ROE ; Young Joo JIN
Journal of Korean Medical Science 1999;14(4):412-416
Endoscopic mucosal resection (EMR) has been standardized for the treatment of intestinal type of intramucosal gastric carcinomas, and careful histological examination of the resected specimen is important for further treatment. To evaluate the diagnostic utility of p53 expression in gastric EMR samples, using immunohistochemical staining, we examined 24 gastric carcinomas (22 intestinal types and two diffuse types) and 20 adenomas removed by EMR. Intestinal type of adenocarcinomas revealed strong p53 expression in 13 cases (59%), weak in four cases (18%), and negative in five cases (23%). Resection margins of 11 carcinomas were involved in the carcinoma cells, which showed the same p53 expression pattern with main carcinoma cells. Squeezed carcinoma cells, remaining in resection margins, were definitely identified by strong p53 expression in seven cases of which the main tumor strongly expressed p53. Microscopic in situ carcinoma could be easily detected in p53 immunostaining. Multifocal involvement and submucosal invasion of carcinomas could be demarcated easily and definitely by strong p53 expression of carcinoma cells. All adenomas showed diffuse weak p53 expression. The difference of p53 expression (p< 0.001) could be used as a differential diagnosis between adenomas and carcinomas. According to these results, we propose that for careful histological examination in hospital diagnosis, both histological evaluation and p53 immunostaining are important diagnostic parameters in EMR samples of the intestinal type of gastric carcinomas.
Adenocarcinoma/surgery
;
Adenocarcinoma/pathology
;
Adenoma/surgery*
;
Adenoma/pathology*
;
Endoscopy*
;
Gastric Mucosa/metabolism
;
Gastric Mucosa/chemistry
;
Human
;
Immunoenzyme Techniques
;
Protein p53/diagnostic use*
;
Protein p53/biosynthesis
;
Protein p53/analysis
;
Stomach Neoplasms/surgery*
;
Stomach Neoplasms/pathology*
;
Tumor Markers, Biological
2.Auriculotemporal and greater auricular nerve blocks have roles in patients with Ramsay Hunt syndrome with trigeminal nerve involvement: A report of two cases.
Hyun Seung JIN ; Woo Seok SIM ; Hee Jin ROE
Anesthesia and Pain Medicine 2012;7(1):16-21
Ramsay Hunt syndrome (RHS) refers to herpes zoster infection of the geniculate ganglion of the facial nerve. Cases complicated by multicranial nerve involvement in the process of reactivation of the virus, which are known to show virulent clinical course and worse prognosis, are not common in literature as in practice, and there has been only one reported case of suspected co-involvement of the trigeminal nerve in Korean literature. Therefore, in cases of RHS with severe rash over the face and neck, it is pertinent to give consideration to such multiple involvement in their early presentation. Facial nerve palsy and herpes related pain are the two worrisome complication, which could be alleviated by early treatment with neural blockade in addition to oral medication. Especially, nerve blocks are known to decrease the extent of nerve inflammation or damage, thereby facilitating recovery and probably preventing postherpetic neuralgia. We report two rare cases of Ramsay Hunt syndrome with trigeminal nerve involvement, where early implementation of blockade of somatic peripheral nerve branches, in addition to the conventional treatment, promoted early recovery.
Exanthema
;
Facial Nerve
;
Geniculate Ganglion
;
Herpes Zoster
;
Herpes Zoster Oticus
;
Humans
;
Inflammation
;
Neck
;
Nerve Block
;
Neuralgia, Postherpetic
;
Paralysis
;
Peripheral Nerves
;
Polyneuropathies
;
Prognosis
;
Trigeminal Nerve
;
Viruses
3.Retraction: The association of KLOTHO gene polymorphism with coronary artery disease in Korean subjects.
Eun Jung RHEE ; Se Yeon KIM ; Chan Hee JUNG ; Byung Jin KIM ; Ki Chul SUNG ; Bum Su KIM ; Won Young LEE ; Jin Ho KANG ; Ki Won OH ; Man Ho LEE ; Sun Woo KIM ; Jung Roe PARK
Korean Journal of Medicine 2009;77(3):382-382
4.Comparison of respiratory mechanics between sevoflurane and propofol-remifentanil anesthesia for laparoscopic colectomy.
Si Ra BANG ; Sang Eun LEE ; Hyun Joo AHN ; Jie Ae KIM ; Byung Seop SHIN ; Hee Jin ROE ; Woo Seog SIM
Korean Journal of Anesthesiology 2014;66(2):131-135
BACKGROUND: The creation of pneumoperitoneum and Trendelenburg positioning during laparoscopic surgery are associated with respiratory changes. We aimed to compare respiratory mechanics while using intravenous propofol and remifentanil vs. sevoflurane during laparoscopic colectomy. METHODS: Sixty patients undergoing laparoscopic colectomy were randomly allocated to one of the two groups: group PR (propofol-remifentanil group; n = 30), and group S (sevoflurane group; n = 30). Peak inspiratory pressure (PIP), dynamic lung compliance (Cdyn), and respiratory resistance (Rrs) values at five different time points: 5 minutes after induction of anesthesia (supine position, T1), 3 minutes after pneumoperitoneum (lithotomy position, T2), 3 minutes after pneumoperitoneum while in the lithotomy-Trendelenburg position (T3), 30 minutes after pneumoperitoneum (T4), and 3 minutes after deflation of pneumoperitoneum (T5). RESULTS: In both groups, there were significant increases in PIP and Rrs while Cdyn decreased at times T2, T3, and T4 compared to T1 (P < 0.001). The Rrs of group PR for T2, T3, and T4 were significantly higher than those measured in group S for the corresponding time points (P < 0.05). CONCLUSIONS: Respiratory mechanics can be adversely affected during laparoscopic colectomy. Respiratory resistance was significantly higher during propofol-remifentanil anesthesia than sevoflurane anesthesia.
Anesthesia*
;
Colectomy*
;
Humans
;
Laparoscopy
;
Lung Compliance
;
Pneumoperitoneum
;
Propofol
;
Respiratory Mechanics*
5.The association of KLOTHO gene polymorphism with coronary artery disease in Korean subjects.
Eun Jung RHEE ; Se Yeon KIM ; Chan Hee JUNG ; Byung Jin KIM ; Ki Chul SUNG ; Bum Su KIM ; Won Young LEE ; Jin Ho KANG ; Ki Won OH ; Man Ho LEE ; Sun Woo KIM ; Jung Roe PARK
Korean Journal of Medicine 2006;70(3):268-276
BACKGROUND: Klotho knock-out mouse is being thought as a good animal model for human aging and these mice show typically severe atherosclerosis of large arteries. Recent studies report on the association of KLOTHO gene mutation with cardiovascular diseases in humans. We observed the frequencies of G395A in promoter and C1818T in exon 4 of KLOTHO gene and investigated their relationships with the presence of coronary artery disease (CAD) in those patients underwent coronary angiograms METHODS: Total 168 subjects (mean age 58 years, 26-87 years) who underwent coronary angiograms due to chest pain were enrolled and blood pressure, body mass index, fasting blood glucose and lipid profiles were measured in all subjects. Genotypings were performed with real-time polymerase chain reaction from sampled blood. RESULTS: The allele frequencies of G395A were 0.872 for G allele and 0.128 for A allele and those of C1818T were 0.830 for C allele and 0.170 for T allele. Both were in compliance with Hardy-Weinberg equilibrium (p=0.99, p=0.82). When the subjects were classified into four groups according to the number of stenotic vessels, there were no differences among the mean values of the cardiovascular risk factors, except high-density lipoprotein cholesterol, that showed a significant difference between that of normal and the diseased vessel groups. There were no differences in the prevalence of CAD according to the genotypes of G395A polymorphism, but for C1818T polymorphism, subjects with T allele showed lower prevalence of CAD than those with CC genotype. When the subjects were divided into two groups according to age, in the group under 60 years of age, T allele carriers of C1818T polymorphism showed lower prevalence of CAD than non-carriers. In the group older than 60 years, A allele carriers of G395A polymorphism showed lower prevalence of CAD than non-carriers. CONCLUSIONS: The frequencies of KLOTHO G395A and C1818T polymorphisms in Koreans were observed similarly to those reported in other Asian races and the phenotypic expression on CAD was different according to age groups. These results infer the possibility of KLOTHO gene as the candidate gene of atherosclerosis in humans, which needs further research.
Aging
;
Alleles
;
Animals
;
Arteries
;
Asian Continental Ancestry Group
;
Atherosclerosis
;
Blood Glucose
;
Blood Pressure
;
Body Mass Index
;
Cardiovascular Diseases
;
Chest Pain
;
Cholesterol
;
Compliance
;
Continental Population Groups
;
Coronary Artery Disease*
;
Coronary Vessels*
;
Exons
;
Fasting
;
Gene Frequency
;
Genotype
;
Humans
;
Lipoproteins
;
Mice
;
Models, Animal
;
Prevalence
;
Real-Time Polymerase Chain Reaction
;
Risk Factors
6.Association between two SNPs (+45T>G and +276G>T) of the adiponectin gene and coronary artery diseases.
Chan Hee JUNG ; Eun Jung RHEE ; Se Yeon KIM ; Hun Sub SHIN ; Byung Jin KIM ; Ki Chul SUNG ; Bum Su KIM ; Won Young LEE ; Jin Ho KANG ; Ki Won OH ; Man Ho LEE ; Sun Woo KIM ; Jung Roe PARK
Korean Journal of Medicine 2006;70(4):393-401
BACKGROUND: Adiponectin, an adipocyte-secreted protein, is known to have anti-atherogenic, anti-inflammatory and anti-diabetic properties. Adiponectin levels are decreased in obesity, type 2 diabetes, and coronary artery disease. Several studies have been performed aiming to investigate the association of genetic variations in the adiponectin with obesity, insulin resistance, and type 2 diabetes but few studies were performed in association with coronary artery disease. Therefore we examined the association between two single nucleotide polymorphisms (SNPs) (+45T>G and +276G>T) of the adiponectin gene and coronary artery diseases (CAD). METHODS: One hundred fifty six subjects were enrolled in which coronary angiograms were performed due to chest pain in Kangbuk Samsung Hospital from April to August, 2003 (97 males, 59 females, mean age 57.40+/-11.15 yrs). Body mass index, fasting blood glucose, lipid profiles were measured in every subject. Single nucleotide polymorphisms (SNPs) in the adiponectin gene were determined by Taqman polymerase chain reaction (PCR) method. The presence of CAD was defined as a >50% reduction of coronary artery diameter. RESULTS: Among 156 subjects, the allele frequencies were 0.683 for G allele and 0.317 for T allele in SNP +276G>T and 0.705 for T allele and 0.295 for G allele in SNP +45T>G. Both genotypes were in compliance with Hardy-Weinberg equlibrium. Mean serum fasting glucose level was significantly higher and mean high-density lipoprotein cholesterol (HDL-C) level was lower in CAD groups (p=0.015, p=0.004). No association with the presence of CAD was observed for adiponectin gene SNP276 and SNP45 (p=0.954, p=0.843). Also, no significant association was observed between the severity of CAD and either SNPs (p=0.571, p=0.955). CONCLUSIONS: Our study showed that SNP +276G>T and +45T>G in adiponectin gene were not associated with the presence of CAD. Further studies will be necessary to confirm the role of SNP 276G>T and 45T>G in the development of CAD.
Adiponectin*
;
Alleles
;
Blood Glucose
;
Body Mass Index
;
Chest Pain
;
Cholesterol
;
Compliance
;
Coronary Artery Disease*
;
Coronary Vessels*
;
Fasting
;
Female
;
Gene Frequency
;
Genetic Variation
;
Genotype
;
Glucose
;
Humans
;
Insulin Resistance
;
Lipoproteins
;
Male
;
Obesity
;
Polymerase Chain Reaction
;
Polymorphism, Single Nucleotide*