1.Perinatal Hypoxic-lschemic Brain Injury: MR Findings.
Journal of the Korean Radiological Society 1994;31(3):405-410
PURPOSE: To characterize the MR findings of hypoxic-ischemic brain injury and to assess the value of the MR imaging. MATERIALS AND METHODS: SE T1 -, T2-weighted, and IR brain MR images of 44 infants and children with the past history of perinatal hypoxic insults were reviewed. Abnormal brain MR findings of 8 patients with birth history of prematurity and 36 patients with birth history of full-term/posterm including 7 with severe anoxic insult history, were compared in regard to the location and the character of the lesions RESULTS: MRI demonstrated the followings;(1)abnormal signal intensity lesions of subcortical and/or deep cerebral white matter, cortex, and deep gray matter, (2)atrophy of the cerebral white matter, cortex and corpus callosum, with/without ventriculomegaly, and (3)delay in myelination. Periventricular and deep white matter lesions were demonstrated in the prematurity, the deep white matter lesions and/or subcortical white matter lesions in the term/post-term, and deep gray matter lesions in the 7 patients with severe anoxic insults history. CONCLUSION: MR imaging was useful in the diagnosis of the hypoxic-ischemic brain injury, and the white and gray matter lesions were correlated with the time of the injury and the severity of hypoxic insult.
Brain Injuries*
;
Brain*
;
Child
;
Corpus Callosum
;
Diagnosis
;
Humans
;
Infant
;
Magnetic Resonance Imaging
;
Myelin Sheath
;
Reproductive History
2.A case of multiple myeloma associated with osteosclerosis.
Chang Kyu LEE ; Hye Kyung KIM ; Kap No LEE
Korean Journal of Clinical Pathology 1991;11(1):103-108
No abstract available.
Multiple Myeloma*
;
Osteosclerosis*
3.Comparison of Oxygenation and Lung Damage of High Frequency Flow Interruption to Conventional Ventilation in Surfactant Deficient Rabbits.
Chang Keun KIM ; Churl Young CHUNG ; Hye Jae CHO
Journal of the Korean Pediatric Society 1995;38(5):591-601
No abstract available.
Lung*
;
Oxygen*
;
Rabbits*
;
Ventilation*
4.A Case of Neonatal Infective Endocarditis without Cardiac Anomaly.
Do Youn KONG ; Hye Kyung LEE ; Young Chang KIM
Journal of the Korean Society of Neonatology 1998;5(1):109-112
Neonatal infective endocarditis is fatal and rare disease but recently there is a trend of an increase in incidence even without congenital heart disease when there are high risk as prematurity, central vein catheterization and neonatal cardiopulmonary resuscitation. Symchych reported that in about 3% of autopsy cases of an year, the findings of infective endocarditis were noted. In Korea, there was a case report but it was case of a premature infant who had umbilical vein catheterization and respiratory ventilator treatment. We experienced a case of neonatal infective endocarditis in a female infant who was delivered at 34 weeks gestational age without receiving central vein catheterization or neonatal cardiopulmonary resuscitation. Although she received intensive antibiotic therapy for staphylococcus cultured in blood, she died necessarily. We reported a case of neonatal infective endocarditis without cardiac anomaly with brief review of related literature.
Autopsy
;
Cardiopulmonary Resuscitation
;
Catheterization
;
Catheters
;
Endocarditis*
;
Female
;
Gestational Age
;
Heart Defects, Congenital
;
Humans
;
Incidence
;
Infant
;
Infant, Newborn
;
Infant, Premature
;
Korea
;
Rare Diseases
;
Staphylococcus
;
Staphylococcus aureus
;
Umbilical Veins
;
Veins
;
Ventilators, Mechanical
5.The Cytologic Features of Desmoplastic Small Round Cell Tumor with Intranuclear Inclusions : A Case Report .
Ho Chang LEE ; Hye Suk HAN ; Ok Jun LEE
Korean Journal of Pathology 2009;43(3):279-284
Desmoplastic small round cell tumor (DSRCT) is a rare neoplasm of young adults and it is characterized by polyphenotypic differentiation. We experienced a case of abdominal DSRCT that occurred in a 19-year-old female who presented with painful swelling of her right forearm. The tumor was cytokeratin-negative and it exhibited some tumor cells with intranuclear inclusions. Molecular demonstration of EWS-WT1 fusion transcripts is particularly useful to confirm the diagnosis of DSRCT without epithelial differentiation. We report here on a case of cytokeratin-negative DSRCT that showed an unusual feature of intranuclear inclusions.
Desmoplastic Small Round Cell Tumor
;
Female
;
Forearm
;
Humans
;
Intranuclear Inclusion Bodies
;
Keratins
;
Young Adult
6.Clinical Case Conference.
Hye Yoon PARK ; Jong Heun KIM ; Se Chang YOON
Journal of Korean Neuropsychiatric Association 2012;51(1):4-15
No abstract available.
7.The Effects of Elliptical Versus Slit Arteriotomy on Patency in End-to-Side Microvascular Anastomosis .
Ji Hye KIM ; Gi Young YUN ; Chang Hyun YOO
Journal of the Korean Society for Vascular Surgery 1999;15(1):22-28
The fashion of vascular anastomosis, end-to-end or end-to-side (E-to-S), are depended upon surgeon's preference or surgical situations. In E-to-S anastomosis two different methods of arteriotomy are applicable but it has been suggested the type, either elliptical or slit arteriotomy, play a different role in the flow hemodynamics. We thought that the difference is more considerable in microvascular surgery. This study examines the effects of elliptical versus slit arteriotomy on morphologic vessel patency. Twenty male Sprague-Dawley rats were divided into two groups of ten rats each. Both carotid arteries were selected as a experimental model. During the procedures the rat brain was tolerable to ischemia and all animals were survived after operations. The morphologic analysis of anastomosis site was through resin-casting method with scanning electromicroscopic examination. The results showed notable difference between two groups in three-dimensional morphology at two-month of operation. This difference may affect the flow hemodynamics and long-term vessel patency. In microvascular anastomosis, the mortpologic difference of the elliptical arteriotomy is worse than slit arteriotomy which compromises the vessel circumference.
Animals
;
Brain
;
Carotid Arteries
;
Hemodynamics
;
Humans
;
Ischemia
;
Male
;
Models, Theoretical
;
Rats
;
Rats, Sprague-Dawley
8.Tricuspid Regurgitation in Heart Diseases in Infants and Children.
Hye Kyung HAN ; Yong Soo YUN ; Chang Yee HONG
Korean Circulation Journal 1988;18(1):127-134
Doppler echocardiography was performed to evaluate the tricuspid regurgitation in 786 infants and children with heart disease. 3 Doppler methods were used. : The duration of systolic turbulence of tricuspid regurgitation in thr right atrium was evaluated by continuous wave Doppler method, the distance of systolic turbulence within right atrium from the tricuspid plane, by pulsed Doppler method and the retrograde systolic hepatic vein regurgitation, by color Doppler method. The following results were obtained. 1) Incidence of pan systolic tricuspid regurgitation in each disease were as follows. 68% of ECD, 66% of Ebstein's anomaly, 54% of pulmonary atresia, 50% of arrhythmia, 45% of ASD, 38% of TAPVR, 15% of VSD, 26% of TOF, 12% of PDA, 13% of normal children. 2) In about 90% of children with tricuspid regurgitation, hepatic vein regurgitation was detected by color Doppler echocardiography.
Arrhythmias, Cardiac
;
Child*
;
Ebstein Anomaly
;
Echocardiography, Doppler
;
Echocardiography, Doppler, Color
;
Heart Atria
;
Heart Diseases*
;
Heart*
;
Hepatic Veins
;
Humans
;
Incidence
;
Infant*
;
Pulmonary Atresia
;
Scimitar Syndrome
;
Tricuspid Valve Insufficiency*
9.Causes of Hydrops Fetalis: Analysis of 149 Autopsy Cases.
Ho chang LEE ; Je G CHI ; Sung Hye PARK
Korean Journal of Pathology 2007;41(2):103-108
BACKGROUND: Hydrops fetalis is defined as abnormal accumulation of serous fluid in two or more fetal compartments, and this malady is known to be associated with various pathologic conditions. METHODS: We collected 149 cases of hydrops fetalis out of 2,312 autopsies, and we tried to elaborate the underlying causes of hydrops fetalis. The diagnosis was based on the material from either antenatal termination or intrauterine death. RESULTS: The relative incidence of hydrops fetalis was 6.44% of all the pediatric autopsies we performed. The gestational age was evenly distributed from 18 to 33 weeks, except for 30 to 31 weeks. There was no sex difference in the incidence of hydrops fetalis. The main causes were cardiovascular diseases (30.9%), cystic hygroma (13.4%), chromosomal anomaly (8.05%), thoracic conditions (7.38%), followed by urinary tract malformation (4.03%), infection (4.03%) and anemia (3.36%). The most common chromosomal anomaly was Turner syndrome and the second one was Down syndrome. CONCLUSION: Since various conditions can be the cause of hydrops fetalis, pathologists should pay attention to elaborate the underlying causes in every single autopsy.
Anemia
;
Autopsy*
;
Cardiovascular Diseases
;
Diagnosis
;
Down Syndrome
;
Edema*
;
Fetus
;
Gestational Age
;
Hydrops Fetalis*
;
Incidence
;
Lymphangioma, Cystic
;
Sex Characteristics
;
Turner Syndrome
;
Urinary Tract