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1.
Journal of Korean Medical Science ; : 34-2020.
Article in English | WPRIM | ID: wpr-782491

ABSTRACT

No abstract available.


Subject(s)
Geriatric Assessment
2.
Endocrinology and Metabolism ; : 179-186, 2019.
Article in English | WPRIM | ID: wpr-763696

ABSTRACT

BACKGROUND: Recently, the triglyceride glucose (TyG) index has been considered a surrogate marker of insulin resistance which is a well-known pathogenic factor in nonalcoholic fatty liver disease (NAFLD). However, few studies have investigated the relationship between the TyG index and NAFLD. Thus, we investigated the relationship between the TyG index and NAFLD and the effectiveness of the TyG index compared with the homeostasis model assessment of insulin resistance (HOMA-IR) in identifying NAFLD in Korean adults. METHODS: Participants of 4,986 who underwent ultrasonography in a health promotion center were enrolled. The TyG index was calculated as ln [fasting triglycerides (mg/dL)×fasting glucose (mg/dL)/2], and HOMA-IR was estimated. NAFLD was diagnosed by ultrasonography. RESULTS: Significant differences were observed in metabolic parameters among the quartiles of the TyG index. The prevalence of NAFLD significantly increased with increment in the TyG index. After adjusting for multiple risk factors, a logistic regression analysis was performed. When the highest and lowest quartiles of the TyG index and HOMA-IR were compared, the odds ratios for the prevalence of NAFLD were 2.94 and 1.93 (95% confidence interval, 2.32 to 3.72 and 1.43 to 2.61; both P for trend <0.01), respectively. According to the receiver operating characteristic analysis, the TyG index was superior to HOMA-IR in predicting NAFLD. CONCLUSION: The TyG index and prevalence of NAFLD were significantly related and the TyG index was superior to HOMA-IR in predicting NAFLD in Korean adults.


Subject(s)
Adult , Humans , Biomarkers , Glucose , Health Promotion , Homeostasis , Insulin Resistance , Insulin , Logistic Models , Non-alcoholic Fatty Liver Disease , Odds Ratio , Prevalence , Risk Factors , ROC Curve , Triglycerides , Ultrasonography
3.
Endocrinology and Metabolism ; : 364-371, 2018.
Article in English | WPRIM | ID: wpr-716968

ABSTRACT

BACKGROUND: Genetic variations in calpain-10 and adiponectin gene are known to influence insulin secretion and resistance in type 2 diabetes mellitus. Recently, several single nucleotide polymorphisms (SNPs) in calpain-10 and adiponectin gene have been reported to be associated with type 2 diabetes and various metabolic derangements. We investigated the associations between specific calpain-10 and adiponectin gene polymorphisms and Korean type 2 diabetes patients. METHODS: Overall, 249 type 2 diabetes patients and 131 non-diabetic control subjects were enrolled in this study. All the subjects were genotyped for SNP-43 and -63 of calpain-10 gene and G276T and T45G frequencies of the adiponectin gene. The clinical characteristics and measure of glucose metabolism were compared within these genotypes. RESULTS: Among calpain-10 polymorphisms, SNP-63 T/T were more frequent in diabetes patients, and single SNP-63 increases the susceptibility to type 2 diabetes. However, SNP-43 in calpain-10 and T45G and intron G276T in adiponectin gene were not significantly associated with diabetes, insulin resistance, nor insulin secretion. CONCLUSION: Variations in calpain-10, SNP-63 seems to increase the susceptibility to type 2 diabetes in Koreans while SNP-43 and adiponectin SNP-45, -276 are not associated with impaired glucose metabolism.


Subject(s)
Humans , Adiponectin , Diabetes Mellitus, Type 2 , Genetic Variation , Genotype , Glucose , Insulin , Insulin Resistance , Introns , Metabolism , Polymorphism, Single Nucleotide
4.
Yeungnam University Journal of Medicine ; : 285-289, 2017.
Article in Korean | WPRIM | ID: wpr-787059

ABSTRACT

Pheochromocytoma can present with various symptoms including cardiogenic shock and cardiac arrest. Particularly, in cases of cardiogenic shock of unknown origin, pheochromocytoma should be considered. A 20-year-old woman without any medical history visited our emergency department due to nausea, vomiting, headache, and chest pain. Echocardiography revealed severe left ventricular dysfunction. Mechanical ventilation and veno-arterial extracorporeal membrane oxygenation (ECMO) were implemented owing to her unstable vital signs. For unstable vital sign and cardiogenic shock in a young woman without any previous medical history, pheochromocytoma was considered and diagnosed based on elevated levels of catecholamine derivatives in a 24-hour urine sample. Cardiac function recovered and ECMO was discontinued on the 5th day of hospitalization. She later underwent an elective adrenalectomy and no recurrence was found during the follow-up period. We reported a case of pheochromocytoma which was presented with cardiogenic shock in a young woman with no concomitant disease, and successfully treated with ECMO followed by an elective adrenalectomy.


Subject(s)
Female , Humans , Young Adult , Adrenalectomy , Chest Pain , Echocardiography , Emergency Service, Hospital , Extracorporeal Circulation , Extracorporeal Membrane Oxygenation , Follow-Up Studies , Headache , Heart Arrest , Hospitalization , Nausea , Pheochromocytoma , Recurrence , Respiration, Artificial , Shock, Cardiogenic , Ventricular Dysfunction, Left , Vital Signs , Vomiting
5.
Yeungnam University Journal of Medicine ; : 115-118, 2017.
Article in Korean | WPRIM | ID: wpr-787037

ABSTRACT

Insulin autoimmune syndrome (IAS) is characterized by spontaneous hypoglycemia, extremely high serum insulin levels, and high titers of autoantibodies against endogenous insulin, in the absence of exogenous insulin injection. IAS often occurs following exposure to sulfhydryl-containing drugs, including alpha-lipoic acid (ALA). A 30-year-old woman without diabetes visited our outpatient clinic with recurrent hypoglycemia. She had been taken ALA for weight reduction since 3 weeks ago. Further hypoglycemia work up revealed very high insulin levels, C-Peptide levels and positive insulin antibodies. And conventional imaging examinations were negative for insulinoma or other pancreatic tumors. Finally, the diagnosis of Insulin autoimmune syndrome (IAS) was made. Following the cessation of ALA, hypoglycemia improved, with no medication, and the patient experienced no further hypoglycemic attacks over the next month. The use of ALA as a nutritional supplement is increasing. We report a case of IAS associated with ALA in a non-diabetic patient.


Subject(s)
Adult , Female , Humans , Ambulatory Care Facilities , Autoantibodies , C-Peptide , Diagnosis , Hypoglycemia , Insulin Antibodies , Insulin , Insulinoma , Thioctic Acid , Weight Loss
6.
Kosin Medical Journal ; : 258-262, 2017.
Article in English | WPRIM | ID: wpr-60693

ABSTRACT

Although benign nerve sheath tumors have been described, primary tracheal schwannomas are extremely rare. We report a case of primary tracheal schwannoma, a rare benign nerve sheath tumor in a 58-year-old man with atypical symptoms of chronic cough, sputum and dyspnea for 2 months. Chest computerized tomography showed a 1.7 cm polypoid lesion in posterior wall of mid trachea. The results of bronchoscopic biopsy and immuno-histo-chemical studies were consistent with schwannoma. A surgical treatment of tumor resection and tracheal reconstruction by end-to-end anastomosis was performed.


Subject(s)
Humans , Middle Aged , Biopsy , Cough , Dyspnea , Nerve Sheath Neoplasms , Neurilemmoma , Sputum , Thorax , Trachea
7.
Yeungnam University Journal of Medicine ; : 115-118, 2017.
Article in Korean | WPRIM | ID: wpr-84527

ABSTRACT

Insulin autoimmune syndrome (IAS) is characterized by spontaneous hypoglycemia, extremely high serum insulin levels, and high titers of autoantibodies against endogenous insulin, in the absence of exogenous insulin injection. IAS often occurs following exposure to sulfhydryl-containing drugs, including alpha-lipoic acid (ALA). A 30-year-old woman without diabetes visited our outpatient clinic with recurrent hypoglycemia. She had been taken ALA for weight reduction since 3 weeks ago. Further hypoglycemia work up revealed very high insulin levels, C-Peptide levels and positive insulin antibodies. And conventional imaging examinations were negative for insulinoma or other pancreatic tumors. Finally, the diagnosis of Insulin autoimmune syndrome (IAS) was made. Following the cessation of ALA, hypoglycemia improved, with no medication, and the patient experienced no further hypoglycemic attacks over the next month. The use of ALA as a nutritional supplement is increasing. We report a case of IAS associated with ALA in a non-diabetic patient.


Subject(s)
Adult , Female , Humans , Ambulatory Care Facilities , Autoantibodies , C-Peptide , Diagnosis , Hypoglycemia , Insulin Antibodies , Insulin , Insulinoma , Thioctic Acid , Weight Loss
8.
Yeungnam University Journal of Medicine ; : 285-289, 2017.
Article in Korean | WPRIM | ID: wpr-222845

ABSTRACT

Pheochromocytoma can present with various symptoms including cardiogenic shock and cardiac arrest. Particularly, in cases of cardiogenic shock of unknown origin, pheochromocytoma should be considered. A 20-year-old woman without any medical history visited our emergency department due to nausea, vomiting, headache, and chest pain. Echocardiography revealed severe left ventricular dysfunction. Mechanical ventilation and veno-arterial extracorporeal membrane oxygenation (ECMO) were implemented owing to her unstable vital signs. For unstable vital sign and cardiogenic shock in a young woman without any previous medical history, pheochromocytoma was considered and diagnosed based on elevated levels of catecholamine derivatives in a 24-hour urine sample. Cardiac function recovered and ECMO was discontinued on the 5th day of hospitalization. She later underwent an elective adrenalectomy and no recurrence was found during the follow-up period. We reported a case of pheochromocytoma which was presented with cardiogenic shock in a young woman with no concomitant disease, and successfully treated with ECMO followed by an elective adrenalectomy.


Subject(s)
Female , Humans , Young Adult , Adrenalectomy , Chest Pain , Echocardiography , Emergency Service, Hospital , Extracorporeal Circulation , Extracorporeal Membrane Oxygenation , Follow-Up Studies , Headache , Heart Arrest , Hospitalization , Nausea , Pheochromocytoma , Recurrence , Respiration, Artificial , Shock, Cardiogenic , Ventricular Dysfunction, Left , Vital Signs , Vomiting
9.
Tuberculosis and Respiratory Diseases ; : 295-301, 2016.
Article in English | WPRIM | ID: wpr-125738

ABSTRACT

BACKGROUND: Specific immunoglobulin E (IgE) sensitization to staphylococcal enterotoxin (SE) has been recently considered to be related to allergic disease, including asthma. Despite studies on specific IgE (sIgE) to SE and its relationship to asthma diagnosis and severity, the association of sIgE to SE with airway hyperresponsiveness (AHR) remains unclear. METHODS: We enrolled 81 asthma patients admitted to the Severance Hospital in Korea from March 1, 2013, to February 28, 2015 and retrospectively reviewed the electronic medical records of the enrolled subjects. The serum levels of sIgE to SE (A/B) of all subjects was measured using the ImmunoCAP 250 (Phadia) system with SE-sIgE positive defined as >0.10 kU/mL. RESULTS: The SE-sIgE level was not significantly correlated with asthma severity (forced expiratory volume in 1 second [FEV₁], FEV₁/forced vital capacity, sputum eosinophils, and serum eosinophils), whereas the SE-sIgE level in patients with positive AHR (mean±standard error of the mean, 0.606±0.273 kU/mL) was significantly higher than that in patients with negative AHR (0.062±0.015 kU/mL, p=0.034). In regression analysis, SE sensitization (sIgE to SE ≥0.010 kU/mL) was a significant risk factor for AHR, after adjustment for age, sex, FEV₁, and sputum eosinophils (odds ratio, 7.090; 95% confidence interval, 1.180–42.600; p=0.032). Prevalence of SE sensitization was higher in patients with allergic rhinitis and non-atopic asthma patients, as compared to patients without allergic rhinitis and atopic asthma patients, respectively, but without statistical significance. CONCLUSION: SE sensitization is significantly associated with AHR.


Subject(s)
Humans , Asthma , Diagnosis , Electronic Health Records , Enterotoxins , Eosinophils , Immunoglobulin E , Immunoglobulins , Korea , Prevalence , Retrospective Studies , Rhinitis, Allergic , Risk Factors , Sputum , Staphylococcus , Vital Capacity
10.
Journal of Korean Academy of Oral Health ; : 167-176, 2012.
Article in English | WPRIM | ID: wpr-70976

ABSTRACT

OBJECTIVES: To assess the effect of glazing materials with different sealants on sealant surface roughness and surface hardness. METHODS: Ultraseal XT(TM) sealant (group 1) and 3M Concise(TM) sealant (group 2) were applied on the buccal surfaces of 26 bicuspid teeth per group. The buccal surface of each tooth was then divided into two half surfaces for 52 halves per group. BisCover LV(TM) glaze was applied to one of the two buccal half surfaces of randomly selected 13 teeth per group. For the other remaining 13 teeth per group, we applied Fortify(TM) glaze to one of the two half surfaces. The remaining 26 buccal half surfaces per group covered with sealant only, did not receive any glaze. The surface roughness and hardness of each sample was measured, and the average value of the three measurements from the individual sample was calculated. The sample surfaces were also observed by scanning an electron microscopy. RESULTS: Two-way ANOVA with surface roughness and hardness as the individual dependent variables identified a statistically significant interaction between the sealants and glazing materials. BisCover LV lowered Ultraseal XT surface roughness and application of surface glazing materials on 3M Concise promoted the hardness. Micro-cracks were identified on the surface in no glaze compared to being less in any glaze. CONCLUSIONS: Surface glaze material could improve the surface roughness and hardness of the selected pit and fissure sealant material. Such a sealant-reinforcing procedure, involving surface glazing, may be clinically useful.


Subject(s)
Acrylates , Bicuspid , Electrons , Hardness , Pit and Fissure Sealants , Resin Cements , Tooth
11.
Korean Journal of Orthodontics ; : 16-26, 2010.
Article in Korean | WPRIM | ID: wpr-653837

ABSTRACT

OBJECTIVE: The purposes of this study were to evaluate the force and stress depending on the type, deflection and thickness of the materials and to evaluate the mechanical properties of thermoplastic materials after repeated loading. METHODS: Four types of thermoplastic products were tested. Force until the deflections of 2.0 mm and the stress when the materials were restoring to its resting position were evaluated. The mechanical properties of thermoplastic materials evaluated after 5 repeated loading cycles. RESULTS: The interaction was observed between the thickness and the deflection (p < 0.05) from the regression equation. Thickness and amount of deflection rather than products and materials showed the largest effect on force and stress. In all products, at least 159 gf of force was required for more than 1.0 mm deflection or when materials with 1.0 mm thickness were deflected. The stress recorded was more than 19 gf/mm2. During repeated loading, each group showed significant difference on the force and the stress p < 0.01), 10 - 17% reduction of force and 4 - 7% reduction of stress in average. CONCLUSIONS: Proper thickness of thermoplastic materials and deflection level of tooth movement should be decided for the physiologic tooth movement. Force decay after repeated loading should be considered for the efficient tooth movement.


Subject(s)
Tooth Movement Techniques
12.
Korean Journal of Gastrointestinal Endoscopy ; : 80-85, 2005.
Article in Korean | WPRIM | ID: wpr-190280

ABSTRACT

Although esophageal tuberculosis is a rare disease throughout the world, esophageal tuberculosis should be included as one of differential diagnosis made in Korea where the prevalence of tuberculosis is still high. Esophageal tuberculosis might be mistaken for carcinoma due to lack of specific symptom, diagnostic study or pathologic diagnosis in clinical setting. The diagnosis would be difficult when esophageal ulcerative lesions or submucosal tumor are present, especially. When the result after a biopsy is not confirmative, the diagnosis can be made with the detection of mycobacteria by microbiologic study or polymerase chain reaction. We experienced three patients with esophageal tuberculosis; a 41-year-old woman with dysphagia, a 34-year-old woman with dysphagia and odynophagia, and a 52-year-old woman with epigastric pain. Esophageal submucosal tumors were found in all the patients with upper gastrointestinal endoscopy. The diagnosis of tuberculosis were finally made by removal of tumor and biopsy or tuberculosis polymerase chain reaction. They all got improved after the treatement with anti-tuberculosis medications. Herein, we report 3 cases of esophageal tuberculosis with review of related literatures.


Subject(s)
Adult , Female , Humans , Middle Aged , Biopsy , Deglutition Disorders , Diagnosis , Diagnosis, Differential , Endoscopy, Gastrointestinal , Korea , Polymerase Chain Reaction , Prevalence , Rare Diseases , Tuberculosis , Ulcer
13.
Journal of the Korean Society of Pediatric Nephrology ; : 213-221, 2005.
Article in Korean | WPRIM | ID: wpr-195630

ABSTRACT

PURPOSE: Urachal anomalies are rare but are known to develop several complications, especially infection. Moreover, uniform guidelines for management have not been presented because of the variable clinical characteristics of these anomalies. The purpose of this report is to review our experience with urachal anomalies and attempt to determine the optimal management. METHODS: We retrospectively reviewed the records of fourteen children with a variety of urachal anomalies who had been treated from January 1996 to June 2005 at Dong Kang General Hospital. RESULTS: The age distribution of the patients(mean age; 3.8 years) was six neonates, one infant, five preschool-age and two school-age children. The male to female ratio was 1:1. Six cases of urachal cyst, four cases of patent urachus, two cases of urachal sinus and two cases of urachal diverticulum were found. Three patients with patent urachus and one with urachal cyst had hydronephrosis. Other associated anomalies included an inguinal hernia in one patient with urachal sinus and a vesicoureteral reflux in one patient with urachal diverticulum. As a first-line diagnostic tool, high-resolution ultrasound examination was performed in thirteen cases and computed tomography in one case. Surgical excision was performed in nine patients with urachal anomaly. Five cases out of six neonatal cases experienced spontaneous improvement during a three-month follow up period. Due to frequent infection of the umbilicus, surgical excision was performed on one neonate with urachal sinus. CONCLUSION: All patients with urachal anomalies should undergo investigation for associated anomalies. The neonate with urachal anomalies, especially patent urachus, do not require surgical excision unless the patient has multiple episodes of recurrent infection.


Subject(s)
Child , Female , Humans , Infant , Infant, Newborn , Male , Age Distribution , Diverticulum , Follow-Up Studies , Hernia, Inguinal , Hospitals, General , Hydronephrosis , Retrospective Studies , Ultrasonography , Umbilicus , Urachal Cyst , Urachus , Vesico-Ureteral Reflux
14.
Korean Journal of Gastrointestinal Endoscopy ; : 156-160, 2004.
Article in Korean | WPRIM | ID: wpr-34268

ABSTRACT

Placement of an endoprosthesis for billiary obstruction has been advocated as an effective alternative for internal-external drainage catheters or surgical procedure. Endoscopic retrograde biliary drainage (ERBD) is a method of transpapillary insertion and placement of drainage tube in the billiary tree under the direct view of endoscope. Early complications following ERBD that develop within 4 weeks include obstruction of the stent, cholangitis, hemorrhage, acute pancreatitis, and bile duct or duodenal perforation. Late complications include obstruction of the stent and cholangitis, migration of the stent, and intestinal perforation. We expierenced a case of sigmoid colonic perforation following ERBD in a patient with multiple biliary tract stone and cholangitis. Thus we report this case with a brief review of the literature.


Subject(s)
Humans , Bile Ducts , Biliary Tract , Catheters , Cholangitis , Colon, Sigmoid , Drainage , Endoscopes , Hemorrhage , Intestinal Perforation , Pancreatitis , Plastics , Stents
15.
Korean Journal of Gastrointestinal Endoscopy ; : 213-217, 2004.
Article in Korean | WPRIM | ID: wpr-33695

ABSTRACT

Insertion of self-expandable metallic stent has been performed as a palliative therapeutic modality for cases with gastrointestinal obstruction caused by inoperable malignancies such as pancreatic cancer, stomach cancer, and cholangiocarcinoma. Although the clinical efficacy is not established yet, it can also be performed for benign gastroduodenal obstruction. Especially, when balloon dilatation is failed and patients are at high risk for surgery or general anesthesia, and when patients refuse operation, insertion of metallic stent can be considered. Complications of this therapeutic modality include intestinal perforation, hemorrhage, migration or malposition of metallic stent, and occlusion of stent by ingrowth and overgrowth of tumor or impaction of food. We report a rare case of obstructive jaundice developed after the insertion of gastroduodenal stent for duodenal obstruction caused by recurrent duodenal ulcer.


Subject(s)
Humans , Anesthesia, General , Cholangiocarcinoma , Dilatation , Duodenal Obstruction , Duodenal Ulcer , Hemorrhage , Intestinal Perforation , Jaundice , Jaundice, Obstructive , Pancreatic Neoplasms , Stents , Stomach Neoplasms
16.
Korean Journal of Pediatrics ; : 1334-1337, 2004.
Article in English | WPRIM | ID: wpr-46064

ABSTRACT

Melanotic neuroectodermal tumor of infancy (MNTI) is a rare neoplasm known by a variety of names including melanotic progonoma and retinal anlage tumor, and currently thought to be neural crest derivation. The vast majority develop within the first year of life. The behavior is generally benign, but recurrent and metastatic cases have been documented. It arises in the head and neck in over 90%, mainly in the maxilla, but is extremely rare in the epididymis. We report a case of MNTI together with a review of literature, which occurred in the right epididymis of a 6-month-old boy who presented with a painless, slowly growing, scrotal mass and was treated with radical orchiectomy.


Subject(s)
Humans , Infant , Male , Epididymis , Head , Maxilla , Neck , Neural Crest , Neuroectodermal Tumor, Melanotic , Orchiectomy
17.
The Korean Journal of Internal Medicine ; : 128-131, 2004.
Article in English | WPRIM | ID: wpr-122271

ABSTRACT

Gallbladder perforation is an almost exclusive complication of cholecystitis, which accompanies severe inflammation of the gallbladder with or without cholelithiasis. Whether it is of a calculous or acalculous origin, gallbladder perforation, as a complication of acute cholecystitis, has common symptoms, signs, laboratory data, radiological findings and treatment modalities. Even though many reports of gallbladder perforation have been published, there are few reports of gallbladder perforation without any clinical and radiological indications. We experienced a case of a 70-year-old woman with acute abdomen, which was found to be peritonitis caused by spontaneous gallbladder perforation that was devoid of clues suggesting this condition. Although rare and unusual, this case shows that this disorder should be considered in elderly patients presenting with peritonitis with an unknown etiology.


Subject(s)
Aged , Female , Humans , Gallbladder Diseases/complications , Peritonitis/diagnosis , Tomography, X-Ray Computed , Ultrasonography, Interventional
18.
Korean Journal of Pediatrics ; : 12-17, 2004.
Article in Korean | WPRIM | ID: wpr-211021

ABSTRACT

PURPOSE: We analyzed pediatric death patients who visited Dong-Kang Hospital emergency center, in order to minimize unexpected pediatric deaths. METHODS: The authors analyzed retrospectively the medical records of 110 pediatric patients who died before and within 24 hours after admission to the emergency center of Ulsan Dong-Kang General Hospital from January 1997 to December 2002. RESULTS: We classified three categories by the cause of death, accident group(AG) 46 cases(41.8%), disease group(DG) 37 cases(33.6%), unknown cause group(UG) 27 cases(24.6%) respectively. The most common age was between two and five years of age(50.0%) in AG, under one month (40.5%) in DG, between one month and one year(51.9%) in UG respectively. The most common season was summer(37.0%) in AG, winter(51.4%) in DG, spring(37.1%) in UG respectively. The most common time on arrival was from 13:00 to 18:00(37.0%) in AG, from 7:00 to noon(43.2%) in DG, from midnight to 6:00(29.6%) and from 7:00 to noon(29.6%) in UG respectively. The most common type of accident was traffic accident(47.8%). The most common cause of death in DG was respiratory disorder(40.5%). Sudden infant death syndrome was the most common(37.1%) in unknown cause of death. CONCLUSION: Accidental injuries and severe chronic illnesses are the major cause of unexpected pediatric death. Legislation related to accidents and a parents teaching program for emergency situations are necessary to decrease cases of unexpected pediatric death.


Subject(s)
Humans , Cause of Death , Chronic Disease , Emergencies , Hospitals, General , Medical Records , Parents , Retrospective Studies , Seasons , Sudden Infant Death
19.
The Korean Journal of Internal Medicine ; : 109-114, 2003.
Article in English | WPRIM | ID: wpr-113822

ABSTRACT

Although acute acalculous cholecystitis (AAC) accounts for less than 10% of acute cholecystitis in the adult population, gangrene and perforation are much more frequent compared to the usual cases of acute cholecystitis (calculus cholecystitis). However, spontaneous biliary-enteric fistula is well recognized in AAC, 90% of which are cholecystoduodenal fistula (CDF) though it is an uncommon disorder. The majority of the CDF are caused by cholelithiasis. As patients are usually associated with complicated clinical illness, the diagnosis is often difficult to make and required surgery is often delayed. We have studied a rare complication of acute acalculous cholecystitis which was presented as intermittent upper gastrointestinal bleeding. Ulceration of the superficial branch of the cystic artery has been observed due to acalculous cholecystitis associated with a cholecystoduodenal fistula. We have performed a transfixing ligation of the bleeding vessel, cholecystectomy and simple closure of the CDF. We have finally made a diagnosis of early gallbladder cancer through a frozen section. There was no serious complication after the operation and the patient has achieved an uneventful recovery.


Subject(s)
Humans , Male , Middle Aged , Acute Disease , Cholecystectomy , Cholecystitis/diagnosis , Duodenal Diseases/complications , Gallbladder Neoplasms/diagnosis , Gastrointestinal Hemorrhage/etiology , Intestinal Fistula/complications
20.
The Korean Journal of Gastroenterology ; : 468-475, 2003.
Article in English | WPRIM | ID: wpr-96877

ABSTRACT

BACKGROUND/AIMS: Genetic polymorphism of cytochrome P450 CYP2C19 influences the efficacy of proton pump inhibitor (PPI) in Helicobacter pylori (H. pylori) eradication therapy. We investigated the difference in the cure rates of H. pylori infection by triple (rabeprazole plus amoxacillin and clarithromycin) therapy in relation to CYP2C19 genotype status. METHODS: One hundred and sixteen H. pylori infected patients with gastric ulcer and duodenal ulcer completed the triple therapy with 10 mg of rabeprazole b.i.d., 1,000 mg amoxacillin b.i.d. and 500 mg of clarithromycin b.i.d. for one week. The genotype of CYP2C19 was determined by a PCR-restriction fragment length polymorphism method. RESULTS: According to the univariate analysis, heterozygous extensive metabolizers (hetero EMs) and poor metabolizers (PMs) showed the highest (87.0%) and the lowest (80.0%) eradication rates, respectively. The difference in the therapeutic efficacy of rabeprazole among the different CYP2C19 genotypes was insignificant. With regard to gender, age and smoking history in relation to eradication rate, a statistical significance was noted only with age with odds ratio of 1.063 and p-value of 0.0202. CONCLUSIONS: In the eradication therapy of H. pylori, no statistically significant difference in therapeutic efficacy of rabeprazole was found among different CYP2C19 genotypes.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , 2-Pyridinylmethylsulfinylbenzimidazoles , Amoxicillin/administration & dosage , Anti-Bacterial Agents/administration & dosage , Anti-Ulcer Agents/administration & dosage , Aryl Hydrocarbon Hydroxylases/genetics , Benzimidazoles/administration & dosage , Clarithromycin/administration & dosage , Drug Therapy, Combination , Duodenal Ulcer/drug therapy , Genotype , Helicobacter Infections/drug therapy , Helicobacter pylori , Mixed Function Oxygenases/genetics , Omeprazole/analogs & derivatives , Proton Pumps/antagonists & inhibitors , Stomach Ulcer/drug therapy
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