1.Clinical Comparison of Neonatal Urinary Tract Infection Caused by Klebsiella pneumoniae Versus Non - klebsiella pneumoniae.
Byeong Il LIM ; Hyeon Jeong CHO ; Ji Yeon HONG ; Woo Ki LEE ; Kwang Woo KIM
Journal of the Korean Society of Neonatology 1999;6(2):193-200
PURPOSE: The purpose of this study was to describe the clinical characteristics of neonatal urinary tract infection (UTI) caused by Klebsiella pneumoniae and non- Klebsiella pneumoniae UTI. METHODS: We compared clinical characteristics of 84 neonatal patients with UTI caused by Klebsiella pneumoniae who were hospitalized at the Department of Pediatricsat Han Dong University, Sunlin Hospital during the period between May, 1994 and August, 1998. The cases were divided into two groups depending upon causative organisms' Klebsiella pneumoniae UTI vs non-Klebsiella pneumoniae UTI, and the clinical characteristics of these groups were compared. RESULTS: Escherichia coli was the most common bacterial pathogen causing neonatal UTI, followed by Klebsiella pneumoniae. There was no significant difference in the sex distribution of Klebsiella pneumoniae UTI, but non-Klebsiella pneumoniae UTI showed male predominence. There were no significant differences in the incidences of hematologic, urologic, radiologic findings and perinatal complications in between these 2 groups. CONCLUSION: Klebsiella pneumoniae is the second most common pathogen causing neonatal UTI. There were no specific differences in the laboratory, symptomatologic, and radiologic findings in these two groups.
Escherichia coli
;
Humans
;
Incidence
;
Klebsiella pneumoniae*
;
Klebsiella*
;
Male
;
Pneumonia
;
Sex Distribution
;
Urinary Tract Infections*
;
Urinary Tract*
2.The Effect of Blue Light and White Light, Continous and Intermittent Phototherapy in the Treatment of Jaundice for the Low Birth Weight Infants.
Ki Tae KIM ; Heon Kyung LEE ; Woo Yeong CHUNG ; Soon Youg LEE ; Yeon Soon KIM
Journal of the Korean Pediatric Society 1983;26(4):299-303
No abstract available.
Humans
;
Infant*
;
Infant, Low Birth Weight*
;
Infant, Newborn
;
Jaundice*
;
Phototherapy*
3.Prognostic Value of Expression of c-erbB-2 in Urinary Bladder Cancer.
Joo Yeon LEE ; Ki Yong SHIN ; Yeung Nam WOO
Korean Journal of Urology 1996;37(7):723-729
C-erbB-2, one of epidermal growth factor receptor gene family, may have an important role in progression of transitional cell carcinoma (TCC of the urinary bladder. We herein immunohistochemically examined 52 bladder TCC specimens for expression of c-erbB-2 gene product to investigate its prognostic value. Interrelationship between expression of c-erbB-2 and stage, grade, expression of proliferating cell nuclear antigen (PCNA), and clinical outcomes were analyzed. Overexpression of c-erbB-2 was significantly higher in invasive tumors as compared with superficial tumors and in high grade tumors as compared with low grade tumors (p<0.005). However, there were no significant correlations between the degree of expression of c-erbB-2 and progression-free survival in patients with superficial bladder TCC as well as actual-survival in patients with invasive bladder TCC. There also was no significant correlation between the expression of c-erbB-2 and PCNA. These results suggest that c-trbB-2 may be an important marker of malignant potentials and invasiveness of bladder TCC, but immunohistochemical study for its expression in bladder TCC may not provide additional prognostic information to stage and grade of the tumors.
Carcinoma, Transitional Cell
;
Disease-Free Survival
;
Genes, erbB-2
;
Humans
;
Proliferating Cell Nuclear Antigen
;
Receptor, Epidermal Growth Factor
;
Urinary Bladder Neoplasms*
;
Urinary Bladder*
4.Adenosis Tumor of the Breast: A Case Report.
Woo Hee JUNG ; Ki Keun OH ; Pyeong Ho YOON ; Mi Kyeong JUNG ; Jung Yeon SHIM
Journal of the Korean Radiological Society 1995;32(5):831-823
Adenosis tumor is a ra re tumor of the breast and primarily consists of adenosis. Authors report a case of surgically proved adenosis tumor in a 31-year-old woman. Mammogram showed a Iobulated, well-circumscribed mass with several surrounding radiolucent halos. In the center of the mass several linear radiolucent densities were seen with the appearance of a conglomerated well-circumscribed mass such as fibroadenoma. These linear radiolucent densities were consistent with the fat between the fibrous sclerosis in pathologic specimen. Ultrasonogram showed a well-circumscribed mass with homogeneous low echogenicity, partial posterior enhancement, and bilateral acoustic shadowings.
Acoustics
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Adult
;
Breast*
;
Female
;
Fibroadenoma
;
Humans
;
Sclerosis
;
Shadowing (Histology)
;
Ultrasonography
5.The Neurocristopathy in a Newborn with Congenital Central Hypoventilation Syndrome, Hirschsprung's Disease and Ganglioneuroblastoma.
Sung Eun JUNG ; Dae Yeon KIM ; Ki Hong KIM ; Seong Cheol LEE ; Kwi Won PARK ; Woo Ki KIM
Journal of the Korean Association of Pediatric Surgeons 1999;5(2):146-151
Neurocristopathy is characterized as having a common origin in aberrant neural crest development. Congenital central hypoventilation syndrome (Ondine's curse) is characterized by marked depression of respiratory drive during sleep and normal ventilation while awake because of no response to both hypercapnea and hypoxia. The girl was full-term, weighing 3020 grams. The girl had poor respiratory effort at birth, but improved with oxygen supply and stimulation. abdominal distention and calcification were noted. During laparotomy transitional zone was found at distal jejunum; a jejunostomy was constructed. Numerous attempts at extubation failed because of apnea. The results of an apnea work-up, including brain sonography, echocardiogram, were normal. The girl died of sepsis at 37 days of age. para-aortic ganglioneuroblastoma was found on autopsy. We experienced a newborn with congenital central hypoventilation syndrome, Hirschsprung's disease and congenital ganglioneuroblastoma representative of neurocristopathy.
Anoxia
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Apnea
;
Autopsy
;
Brain
;
Depression
;
Female
;
Ganglioneuroblastoma*
;
Hirschsprung Disease*
;
Humans
;
Hypoventilation*
;
Infant, Newborn*
;
Jejunostomy
;
Jejunum
;
Laparotomy
;
Neural Crest
;
Oxygen
;
Parturition
;
Sepsis
;
Ventilation
6.Arthrocopic Reconstruction of the Posterior Cruciate Ligment: The Effects of femoral attachment points and knee flexion angles at the time of graft fixation on posterior stability
Sung Il BIN ; Key Yong KIM ; Woo Shin CHO ; Ki Kwang CHEONG ; Woo Yeon HWANG ; Jong Hi PARK
The Journal of the Korean Orthopaedic Association 1995;30(5):1164-1170
The purpose of this study is to compare the effects of the femoral attachment points of the graft and knee flexion angles at the time of graft fixation on stability of posterior cruciate ligament reconstruction. We analyzed the posterior stability of the knee on 23 patients(24 knees) with posterior cruciate ligament injury whose posterior cruciate ligament had been reconstructed arthroscopically and followed for minimum 1 year period at Asan Medical Center from May 1992 to June 1994. The patients were divided into the two groups according to femoral attachment points of the graft and knee flexion angles at the time of graft fixation. The distance from the junction of the intercondylar notch with trochlear groove of the femoral attachment points and knee flexion angles were 11mm and 0°-30° in group A and 7mm and 70°-90° in group B, respectively. 11 knees were included in group A and 13 knees in group B. Posterior stability was determined by difference in posterior tibial translation between the injured and the opposite knee with Telos device. In group A, 5 cases were at the range of 0-2mm, 3 cases 3-5 mm, 3 cases 6-10mm. In group B, 10 cases were at the range of 0-2mm and 3 cases 3-5mm, respectively. Differences in posterior tibial translation on average were 3.6mm and 1.7mm in group A and B, respectively. Conclusively, arthroscopic postrior cruciate ligament reconstruction with femoral attachment point at 7mm from the junction of interconlylar notch with trochlear groove and 70°
Chungcheongnam-do
;
Humans
;
Knee
;
Ligaments
;
Posterior Cruciate Ligament
;
Transplants
7.Two Cases of Congenital Paraesophageal Hiatal Hernia in Infancy.
Ji Yeon HONG ; Kih Yeon SONG ; Kwang Woo KIM ; Woo Ki LEE ; Jong Gon HA ; Soon Ok CHOI
Journal of the Korean Pediatric Society 2000;43(12):1613-1620
Herniation of the stomach through the esophageal hiatus into the posterior mediastinum is a commom affliction of humans. The incidence of hiatal hernia is difficult to determine because of the absence of symptoms in a large number of patients. Hiatal hernias are classified into two major types; type I sliding hiatal hernia and type II paraesophageal hiatal hernia. Sliding hernia is common, but paraesophageal hernia(PEH) is rare. Most PEH is demonstrated in elderly women. PEH in infancy is really rare. PEH is a true hernia, so it is a potentially life-threatening condition because of the risk of volvulus, incarceration, strangulation, and perforation. PEH is itself the indication for surgery. We experienced congenital PEH in two infants. One case was nearly asymptomatic, found incidentally by plain chest X-ray taken for pneumonia in a 12 month old female infant. She had no vomiting or reflux, but history of frequent feeding of small amount and often gurgling noise in her right chest. She had type IV PEH including herniation of the transverse colon. Another case was presented because of vomiting, and was diagnosed by ultrasonography initially in a 48 day old male infant. He had intrathoracic stomach, type III PEH with idiopathic hypertrophic pyloric stenosis and gastroesophageal reflux.
Aged
;
Colon, Transverse
;
Female
;
Gastroesophageal Reflux
;
Hernia
;
Hernia, Hiatal*
;
Humans
;
Incidence
;
Infant
;
Intestinal Volvulus
;
Male
;
Mediastinum
;
Noise
;
Pneumonia
;
Pyloric Stenosis, Hypertrophic
;
Stomach
;
Thorax
;
Ultrasonography
;
Vomiting
8.A case of combined hyperlipoproteinemia.
Young Bae KWON ; Sung Hee IHM ; Moon Ki CHOI ; Byung Tae KIM ; Yeon Bok JANG ; Sung Woo PARK
Journal of Korean Society of Endocrinology 1991;6(2):191-195
No abstract available.
Hyperlipoproteinemias*
9.A case of tracheo-bronchial amyloidosis.
Sung Woon KWON ; Yong Kyun KIM ; Kwang Ho JUNG ; Dong Soon KIM ; Woo Ki JEON ; Yeon Lim SUH
Korean Journal of Medicine 1993;45(5):690-695
No abstract available.
Amyloidosis*
10.A Case of Patent Urachus.
Heon Kyung LEE ; Ki Tae KIM ; Woo Yung CHUNG ; Soon Yong LEE ; Yung Sik PARK ; Yeon Soon KIM
Journal of the Korean Pediatric Society 1984;27(1):89-92
No abstract available.
Urachus*