1.A Study on Red Cell Distribution Width of Iron Deficiency Anemia in Childhood.
Hong Ryang KIL ; Young Hun CHUNG
Journal of the Korean Pediatric Society 1988;31(10):1321-1327
No abstract available.
Anemia, Iron-Deficiency*
;
Erythrocyte Indices*
;
Iron*
2.Prefrontal Cortex and Schizophrenia.
Young Chul CHUNG ; Hong Bae EUN
Journal of the Korean Society of Biological Psychiatry 1998;5(2):184-196
With a rapid development of neuroscience, the theories related to the pathophysiology of schizophrenia have been changed a lot from a simple hyperdopaminergic one to the various complicated ones. Among these, the theories regarding prefrontal cortex(PFC) pathology as a cause of schizophrenia are gaining more recognition as the results of neuroimaging and neuropsychological tests in schizophrenia consistently report abnormalities in PFC. Therefore, we first reviewed the unique characteristics of PFC in anatomy, neurochemistry and neurophysiology to enhance an understanding of those ones. Secondly, various neurotransmitter, neurodevelopmental and neural network theories of schizophrenia introduced recently were reviewed in terms of PFC pathology.
Dopamine
;
Neurochemistry
;
Neuroimaging
;
Neurophysiology
;
Neuropsychological Tests
;
Neurosciences
;
Neurotransmitter Agents
;
Pathology
;
Prefrontal Cortex*
;
Schizophrenia*
3.The Clinical Evaluation of Pars Plana Vitrectomy in various Ocular Disease.
Hwang Ki KIM ; Hong Young CHUNG ; Young Tea CHUNG
Journal of the Korean Ophthalmological Society 1997;38(11):2020-2027
We reviewed the hospital records of 104 consecutive eyes in 101 patients who underwent pars plana vitrectomy at Presbyterian Medical Center from January 1993 to December 1995 and studied the postoperative visual acuity and postoperative complications. Possible indications for pars plana vitrectomy were follows: complications of proliferative diabetic retinopathy (30.7%),complications of other types of proliferative retinopathy except proliferative diabetic retinopathy(25.0%),complications of anterior segment surgeries (14.4%), complex retinal detachments(8.7%), intraocular inflammations and uveitis (8.7%), macular diseases (6.7%), and complications of ocular trauma (5.8%), Regarding postoperative final visual acuity, 53 eyes(51.0%) were improved, 30eyes(28.8%) were stabilized, 21eyes(20.2%) were worsened. Intraoperative or postopertive cataract, retinal breaks or retinal detachment were most frequent complications. We expected that pars plana vitrectomy might be indicated in various ocular diseases containing proliferative diabetic retinopathy.
Cataract
;
Diabetic Retinopathy
;
Hospital Records
;
Humans
;
Inflammation
;
Postoperative Complications
;
Protestantism
;
Retinal Detachment
;
Retinal Perforations
;
Retinaldehyde
;
Uveitis
;
Visual Acuity
;
Vitrectomy*
4.Postoperative outcome of trans pars pklana vitrectomy in the treatment of posterior and intermediate uveitis.
Hong Young CHUNG ; Young Tea CHUNG
Journal of the Korean Ophthalmological Society 1997;38(11):2009-2015
We performed standard pars plana vitrectomies in 17 eyes with uveitis which were complicated with vitreous opacities. Postoperatively, visual acuity was improved in 11 eyes(64.7%),maintained in4 eyes(23.5%) and decreased in 2 eyes (11.8%). Four weeks after vitrectomy, inflammatory cells were rarely noticed in the anterior vitreous of all eyes. We suggest that early surgical approach is of value for visual improvement in the management of uvitis eyes with vitreous opacity.
Uveitis
;
Uveitis, Intermediate*
;
Visual Acuity
;
Vitrectomy*
5.Normolipemic Tendinous and Tuberous Xanthomatosis: One Case Report
Chi Jung KANG ; Snag Ho HA ; Sang Hong LEE ; Young Ju CHUNG ; Chang Young CHUNG
The Journal of the Korean Orthopaedic Association 1989;24(5):1512-1515
A xanthoma is a localized collection of tissue histiocytes containing lipid and is usually associated with hyperlipidemia. Tendinous and tuberous xanthomatosis have been found in association with familial hypercholesterolemia, Type III hyperlipidemia, beta-sitosterolemia and cerebrotendinous xanthomatosis. Tendinous and tuberous xanthomatosis without hyperlipidemia have been reported very rarely. Especially tendinous xanthomatosis without hyperlipidemia have not been reported at all in korea. We are reporting a patient with tendinous and tuberous xanthomatosis accompanied by normal plasma lipids
Histiocytes
;
Humans
;
Hyperlipidemias
;
Hyperlipoproteinemia Type II
;
Korea
;
Plasma
;
Xanthomatosis
;
Xanthomatosis, Cerebrotendinous
6.Ultrastructural Changes in the Exocrine and Endocrine Cells of Rat Pancreas in Endotoxin Shock.
Kun Young KWON ; Chai Hong CHUNG ; Tae Joong SOHN
Korean Journal of Pathology 1985;19(3):255-289
This study was carried out to investigate the morphological changes in the exocrine and endocrine glands of rat pancreas treated with endotoxin. Thirty-five male Sprague-Dawley rats, maintained on a stock diet, weight 200.0 gm. average. were divided into two experimental groups. Group 1. Control group. Five rats. Intraperitoneal infections of 0.3 ml normal saline only. Group 2. Endotoxin-treated group. Thirty rats. 7.6 mg of endotoxin per kg. of body weight was administered intraperitoneally. Each of 5 experimental animal was sacrificed 30 minutes, 1, 2, 4, 6 and 8 hours after endotoxin treatment, followed by examinations of histochemical, light and electron microscopy of both transmission and scanning modes. The results were as follows: A. Light microscopic findings: A mild interstitial edema and hyperemia were noted 1-hour after endotoxin treatment. Cytoplasmic vacuolization at 2-hour level(2-hours after endotoxin administration), diminished staining quality of both endocrine and exocrine cells at 6-hour level. B. Electron microscopic examination: a. Transmission electron microscopy. The acinar cells of pancreas showed a mildly increased pre-lysosome at 30-minute level. At 1-hour level, appearance of secondary lysosome was noted in addition to the findings of mitochondrial swelling and decreased cristae; disarray and vacuolization of the RER; vacuolar change of Golgi apparatus. At 6-hour level, post-lysosomes. The changes in the endocrine glands were similar to the findings of exocrine glands just described with time lag of 1 to 2 hours. The endothelial cells of capillaries show swelling and pinocytotic vesicle formation, protrusion of the cytoplasmic processes into the capillary lumen and increased heterochromatin at 1-hour level. These findings became more prominent as time lapses. The lumen of the endothelium tends to be narrowed, filled with fibrin and other blood cell components which later terminated with occasional complete occlusion by the formation of thrombi. b. Histochemical study: Primary lysosomes of the control group revealed a strong reaction of the acid phosphatase whereas the endotoxin treated group with less reactivity limited in the peripheral zones of the lysosomes. Secondary lysosomes with partial reactions. However, the pre-lysosomes and post-lysosomes failed to demonstrate any acid phosphatase activity at all. c. Scanning electron microscopy. The endothelial cells of the capillaries, arterioles and venules demonstrated increased microvillous activity, broad bled formation, cytoplasmic protrusion into the luminal spaces and microthrombi formation at 1-hour level. Six-hour level onward there noted a junctional disruption and partial detachment from the subendothelium of the wall. It can be concluded, therefore: When the endotoxin enters the blood stream, it elicits endothelial injury followed by both exudation with resultant edema of the surrounding tissue and concomitant vascular occlusions due to thrombosis. This vascular occlusion, in turn, causes ischemic degenerative change of the cells of exocrine and endocrine glands of the pancreas which are followed by digestions of degradational materials from the injured cells through the lysosomal phagocytic system. Besides the above pathogenetic pathway, one can not rule out the possibility of the direct effects of the endotoxin to the cells of exocrine and endocrine cells of the pancreas also so rendered.
Male
;
Humans
;
Rats
;
Animals
7.Mucha - Habermann's Disease ( Pityriasis Lichenoides et Varioliformis Acuta ): Report of A Case.
Young Chan CHOI ; Hong Sang CHIN ; Chung Koo CHO
Korean Journal of Dermatology 1976;14(4):389-393
Muchz-Habermann disease is cutaneous disease of unknown etilogy and characterized by a, polymorphous eruption consisting of papulosquamous, bemorrhagic, ulceronecrotic lesion eventually into varioliform scars. It is also classified into parapsoriasis group according to Broq with parapsoriasis en guttata (pityriasis lichenoides chronica), parapsoriasis en plaques, parapsoriasis en lichenoides. The 61-year-old male patient visited to Dermatologic Department of Severance Hospital due to sudden onset of generalized eruption. He presented pea to fingr tip sized erythematous, silvery maculo-papulo-squamous eruptions on trunk, extre- mities and buttock, but didnt complain of any subjective symptoms except markel fatigue. Skin biopsy was done on right forearm and was confirrr.ed to pityriasis lichenoides et varioliformis acuta by histopathologic finding. The lesion was completely controlled by oral tetracycline 2. Ogm per daily for first 4 wecks and reduced dosage l. Ogin per day for second 2 weeks.
Biopsy
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Buttocks
;
Cicatrix
;
Fatigue
;
Forearm
;
Humans
;
Male
;
Middle Aged
;
Parapsoriasis
;
Peas
;
Pityriasis Lichenoides*
;
Pityriasis*
;
Skin
;
Tetracycline
8.Pneumomediastinum developed during anesthesia.
Mee Young CHUNG ; Hee Soon KIM ; Sung Jin HONG
The Korean Journal of Critical Care Medicine 1991;6(2):131-134
No abstract available.
Anesthesia*
;
Mediastinal Emphysema*
9.Congenital Agenesis of Odonteid Process: A Case Report
Young Min KIM ; Chung Yong HONG ; Seong Ho HAN
The Journal of the Korean Orthopaedic Association 1976;11(2):281-285
Anomalous development of the odonteid precess is an uncommon clinical occurence that can seriously impair the integrity af the atlantoaxial articulation. Absence of the odontoid process may be either congenital or acquired, but clinically the etiology is of little importance as the clinical signs and symptoms and the treatment are identical in both. We experienced a case of congenital absence of the odontoid process and good result was obtained from the posterior atlantoaxial fusion with hale-cast.
Odontoid Process
10.Osteogenesis Imperfecta Tarda (Case Report Tow cases)
Chung Nam KANG ; Ki Hong CHOI ; Young Man PARK
The Journal of the Korean Orthopaedic Association 1976;11(3):309-315
Two cases report on osteogenesis imperfecta tarda and review of literature has been made. The rare genetic disorder, osteogenesis imperfecta tarda is familiar to most orthopedic surgeons because of management of fracture and skeletal deformities, espicially bowing of long bone. Its clinical manifestations are known as bony fragility, blue sclera and deafness less frequently ligamentous laxity but its etiological factor is obscure; The basic defect is thought to involvement some abnormality of collagen. Recently the bony weakness caused by increased bony turnover rate. One case of osteogenesis imberrfecta tarda in 8 year old male was belonged to tarda type 1. (Falvo-classification), who could not walk due to marked anterolateral bowing of right tibia and the another to tarda type II. in 13 year old male with fresh fracture of right femoral shaft. The former was performed corrective multible osteotomy, realignment and intramedullary rod fixation for correction of bowing deformity of right tibia, and the later was managed the fracture of right femoral shaft with Russels traction and hip spica cast. The result of reported therapeutic mesure was good.
Collagen
;
Congenital Abnormalities
;
Deafness
;
Fibrinogen
;
Hip
;
Humans
;
Ligaments
;
Male
;
Orthopedics
;
Osteogenesis Imperfecta
;
Osteogenesis
;
Osteotomy
;
Sclera
;
Surgeons
;
Tibia
;
Traction