1.Hamartoma Arising in the Urinary Bladder: A case report.
Young Bae KIM ; Tae Sook HWANG ; Byung Gon PARK ; Jin Sook JEONG ; Sook Hee HONG
Korean Journal of Pathology 1993;27(3):283-286
Hamartoma of the bladder is quite a rare entity which is composed of a disorderly admixture of mature cellular elements normally present in the urinary bladder. There is a great controversy regarding the pathogenesis of this lesion. Whether it is a true hamartomatous lesion or metaplastic lesion developed secondary to the inflammatory process. Similar or identical lesions has often been given by other names such as florid examples of cystitis glandularis. We prefer to cell florid examples of cystitis glandularis rather than hamartoma when it was occurred in an old age higher then 50th decade. Here we report a case of hamartoma of the urinary bladder in 44 years old man. Cystoscopic examination revealed a papillary polypoid mass which was attached to the fundus of bladder by long stalk. The mass measured 1.5 cm in greatest diameter. It was composed of epithelial nests resembling von Brunn's nest, cystitis glandularis or cystitis cystica dispersed in a stroma rich in smooth muscle and fibrous tissue.
Hamartoma
2.A Case of Intestinal Malrotation Complicated by Midgut Volvulus: Diagnosis with Abdominal CT Scan.
Byung Ju KIM ; Mi Jeong HWANG ; Jae Sook MA
Journal of the Korean Pediatric Society 1997;40(1):140-143
Intestinal malrotation is a constellation of a wide spectrum of embryologic failures of rotation and fixation of the gut, resulting in a narrow-based attachment of the mesentery and the presence of abnormal peritoneal (Ladd's) band. These abnormalities predispose to midgut volvulus, intestinal obstruction and internal herniation. We experienced a case of intestinal malrotation complicated by midgut volvulus in a 4-year-old girl who presente with abdominal pain, abdominal distension and melena. The diagnosis was made by abdominal CT scan, which showed "whirl sign." The diagnosis was confirmed by surgery. A brief review of literature ensues.
Abdominal Pain
;
Acidosis
;
Acidosis, Renal Tubular*
;
Adolescent
;
Alkalies
;
Anemia, Hemolytic
;
Atrophy
;
Biopsy
;
Chest Pain
;
Child, Preschool
;
Diagnosis*
;
Exanthema
;
Female
;
Fever
;
Fibrosis
;
Hospitalization
;
Humans
;
Hypergammaglobulinemia
;
Hypokalemia
;
Intestinal Volvulus*
;
Leukopenia
;
Liver Diseases
;
Lupus Erythematosus, Systemic*
;
Lymphopenia
;
Melena
;
Mesentery
;
Molecular Weight
;
Multiple Myeloma
;
Nephrotic Syndrome
;
Neutrophils
;
Potassium
;
Prednisolone
;
Proteinuria
;
Thyroid Diseases
;
Tomography, X-Ray Computed*
3.A Case of Intestinal Malrotation Complicated by Midgut Volvulus: Diagnosis with Abdominal CT Scan.
Byung Ju KIM ; Mi Jeong HWANG ; Jae Sook MA
Journal of the Korean Pediatric Society 1997;40(1):140-143
Intestinal malrotation is a constellation of a wide spectrum of embryologic failures of rotation and fixation of the gut, resulting in a narrow-based attachment of the mesentery and the presence of abnormal peritoneal (Ladd's) band. These abnormalities predispose to midgut volvulus, intestinal obstruction and internal herniation. We experienced a case of intestinal malrotation complicated by midgut volvulus in a 4-year-old girl who presente with abdominal pain, abdominal distension and melena. The diagnosis was made by abdominal CT scan, which showed "whirl sign." The diagnosis was confirmed by surgery. A brief review of literature ensues.
Abdominal Pain
;
Acidosis
;
Acidosis, Renal Tubular*
;
Adolescent
;
Alkalies
;
Anemia, Hemolytic
;
Atrophy
;
Biopsy
;
Chest Pain
;
Child, Preschool
;
Diagnosis*
;
Exanthema
;
Female
;
Fever
;
Fibrosis
;
Hospitalization
;
Humans
;
Hypergammaglobulinemia
;
Hypokalemia
;
Intestinal Volvulus*
;
Leukopenia
;
Liver Diseases
;
Lupus Erythematosus, Systemic*
;
Lymphopenia
;
Melena
;
Mesentery
;
Molecular Weight
;
Multiple Myeloma
;
Nephrotic Syndrome
;
Neutrophils
;
Potassium
;
Prednisolone
;
Proteinuria
;
Thyroid Diseases
;
Tomography, X-Ray Computed*
4.The Association between Unexplained Second-Trimester Human Chorionic Gonadotropin Elevations and Pregnancy Outcome.
Jae Woong HWANG ; Seong Un JEONG ; Jeong Wook SEO ; Yun Seok YANG ; Jun Sook PARK
Korean Journal of Obstetrics and Gynecology 1998;41(11):2790-2794
We conducted this cohort analytic study to determine whether women with unexplained elevations of maternal serum hCG at 15-18 weeks' gestation are at increased risk for pregnancy complications and adverse perinatal outcomes. The inclusion criteria were a singleton gestation, a confirmed gestational age, and an hCG level greater than 2.0 multiples of the median (MoM). The exclusion criteria were fetal anomalies, an abnormal karyotype, molar pregnancy, and an MSAFP level greater than 2.5 multiples of the median (MoM). A group of randomly selected women with hCG levels under 2.0 MoM served as controls. Patients with elevated levels of hCG had a significantly higher risk for PIH (17.9% versus 4.5%; P <.05) and preterm delivery (17.9% versus 3.5%; P<, 05) than control. But no significant differences were observed in the incidence of intrauterine growth restriction and low birth weight and in the newborn weight. We suggested that pregnancies with unexplained elevated hCG levels should be regarded as high-risk pregnancies. And these patients require careful monitoring with adequate obstetric management.
Abnormal Karyotype
;
Chorionic Gonadotropin*
;
Cohort Studies
;
Female
;
Gestational Age
;
Humans*
;
Hydatidiform Mole
;
Incidence
;
Infant, Low Birth Weight
;
Infant, Newborn
;
Pregnancy
;
Pregnancy Complications
;
Pregnancy Outcome*
;
Pregnancy*
;
Pregnancy, High-Risk
5.A Case of Duplication 9q Syndrome.
Mi Jeong HWANG ; Young Youn CHOI ; Jae Sook MA ; Tai Ju HWANG
Journal of the Korean Society of Neonatology 1998;5(2):193-197
Since the first description of the trisomy 9p in 1970, over one hundred cases have been described with the advanced chromosomal banding technique. Clinical findings include growth and mental retardation and facial dysmorphism. Crucial determinants of the classical features of this syndrome lie within the distal half of the chromosome 9 short arm. But this syndrome has not been reported in Korea, we are reporting a boy diagnosed by clinical features and chromosomal study that is trisomic for a partial short arm of a chromosome 9. A brief review of the literature is included.
Arm
;
Chromosomes, Human, Pair 9
;
Humans
;
Intellectual Disability
;
Korea
;
Male
;
Trisomy
6.A Case of Fatal Intracranial Hemmrhage due to Vitamin K Deficiency.
Yong Sang YOO ; Moon Tae JEONG ; Jai Sook MA ; Tai Ju HWANG
Journal of the Korean Pediatric Society 1986;29(1):108-112
No abstract available.
Vitamin K Deficiency*
;
Vitamin K*
;
Vitamins*
7.Cardiovascular Risk Factors Predicting Endothelial Dysfunction in Patients with Variant Angina.
Sook Hee CHO ; Seon Young HWANG ; Myung Ho JEONG
Journal of Korean Academy of Adult Nursing 2009;21(5):477-488
PURPOSE: This study was conducted to identify the clinical characteristics and risk factors on the occurrence of variant angina, and to examine the predicting factors on the vascular endothelial dysfunction of the patients with variant angina. METHODS: A total of 134 patients diagnosed with variant angina were recruited from 2006 to 2008. The degrees of endothelial dysfunction were measured and recorded by the researcher using the values of flow-mediated vasodilation of their brachial arteries and Nitroglycerine-mediated dilation. Subjects' demographic data and risk factors were gathered after obtaining informed consent, and their electronic medical records were reviewed to collect laboratory data. RESULTS: The mean age was 54.2 +/- 9.6 years and 52% was male patients. More than 50% of the male patients were cigarette smokers and had hypercholesterolemia. 84% of the male patients and 70% of the female patients had more than one risk factor of cardiovascular disease. A stepwise multiple regression analysis showed that smoking and hypercholesterolemia predicted the decrease of flow-mediated vasodilation (Adjusted R(2) = .204, p < .001). CONCLUSION: Tailored educational interventions for smoking cessation and cholesterol management are needed to prevent recurrence of angina attack for patients with variant angina and to prevent cardiovascular disease for middle-aged workers.
Angina Pectoris, Variant
;
Brachial Artery
;
Cardiovascular Diseases
;
Cholesterol
;
Electronic Health Records
;
Female
;
Humans
;
Hypercholesterolemia
;
Informed Consent
;
Male
;
Recurrence
;
Risk Factors
;
Smoke
;
Smoking
;
Smoking Cessation
;
Tobacco Products
;
Vasodilation
8.Patient Outcomes according to Blood Glucose Level in Neonates with Cardiovascular Surgery.
Jeong Hye HWANG ; Hyoung Sook PARK
Journal of Korean Academy of Child Health Nursing 2012;18(1):43-52
PURPOSE: The purpose of this study was to provide basic data for suitable neonate blood glucose maintenance by investigating and analyzing the blood glucose level of post cardiovascular surgery neonates in the ICU for the effect of blood glucose levels on the following outcomes; ICU stay, hospital stay, mechanical ventilation time, morbidity, and mortality. METHODS: The participants were 143 neonates in the ICU after having had cardiovascular surgery. The design for this study was an investigation of the blood glucose levels of the neonates and retrospective analysis of patient outcomes according to blood glucose level. RESULTS: The results for the neonate groups showed that the factors of hospital stay, ICU stay, mechanical ventilation time and mortality, for the group with a blood glucose level over 140 mg/dL were longer and higher than for the group with blood glucose of less than 100 mg/dL or the group between 100-139 mg/dL. CONCLUSION: The results of this study indicate that when caring for neonates after cardiovascular surgery, it is important to recognize the influence of blood glucose levels on patient outcomes like hospital days, ICU stay, length of time on mechanical ventilation and mortality. Further, care guidelines for neonates' glucose level management need to be developed.
Blood Glucose
;
Glucose
;
Humans
;
Infant, Newborn
;
Length of Stay
;
Respiration, Artificial
;
Retrospective Studies
;
Child Health
9.Incidence and Predictors of Cataract among People with Type 2 Diabetes Mellitus: Using Secondary Data Analysis from the Ansan Cohort of the Korean Genome and Epidemiology Study
Ihn Sook JEONG ; Eun Joo LEE ; Myo Sung KIM ; Jung Ok YU ; Hae Sun YUN ; Jeong Hee JEONG ; Youn Sun 6 HWANG
Journal of Korean Academy of Nursing 2022;52(1):24-35
Purpose:
This study investigated the incidence and risk factors of cataract in people with diabetes mellitus (DM) using data from Ansan cohort of the Korean Genome and Epidemiology Study (KoGES).
Methods:
Data from a total of 329 patients with type 2 DM without cataract who participated in Ansan cohort of the KoGES from baseline survey (2001–2002) to fifth follow-up visit (2011–2012) were examined.The characteristics of the subjects were analyzed with frequency and percentage, and mean and standard deviation. Cataract incidence was measured as incidence proportion (%). For risk factors of cataract, hazard ratio (HR) and 95% confidence interval (CI) were obtained using the Cox proportional hazard model.
Results:
The cataract incidence over a 10-year follow-up period was 19.1% (15.1 in males and 25.8 in females), and mean age at the incidence of cataract was 63.48 years (61.58 years in males and 65.31 years in females). Age (HR=1.09, 95% CI=1.05–1.13) and HbA1c (HR=1.21, 95% CI=1.07–1.37) or the duration of DM (HR=1.05, 95% CI=1.00–1.09) were found to be independently associated with cataract development.
Conclusion
Cataract development in people with DM is common, and its likelihood increases with age, HbA1c, and the duration of DM. Considering negative effect of cataract on their quality of life and economic burden, nurses should identify people with DM at a higher risk of cataract development, and plan individual eye examination programs to detect cataract development as early as possible.
10.A Case of Bronchial Mucoepidermoid Carcinoma in Child.
In Jeong KIM ; Jin Soo HWANG ; In Seok KIM ; Byung Ju KIM ; Jae Sook MA
Journal of the Korean Pediatric Society 1999;42(4):580-583
Bronchial mucoepidermoid carcinoma is very rarely encountered in children. We report a case of bronchial mucoepidermoid carcinoma in a 10-year-old boy who presented with persistent cough and atelectasis. Bronchoscopic examination showed a tumor mass occluding the right bronchus intermedius, and the mass was removed by bronchoscopy. The results of the pathological examination revealed low-grade mucoepidermoid carcinoma. He underwent right middle and lower lobectomy with bronchoplasty, and there was no metastasis. He remains symptom-free without recurrence of bronchial tumor during the follow-up period of 12 months.
Bronchi
;
Bronchoscopy
;
Carcinoma, Mucoepidermoid*
;
Child*
;
Cough
;
Follow-Up Studies
;
Humans
;
Male
;
Neoplasm Metastasis
;
Pulmonary Atelectasis
;
Recurrence