1.Changes and Trends in the Newly Established Clinics in Korea.
Byung Soon CHOI ; Ok Ryun MOON
Korean Journal of Preventive Medicine 1992;25(4):357-373
After medical insurance came into effect in Korea, health care system has undergone tremendous changes. Changing patterns of newly established clinics is one of them. To investigate changes and trends, a total of 10,184 clinics which were newly established from 1981 to 1990 were analysed. Data were obtained from the file of contracting medical facilities of the Federation of Medical Insurance Societies. The proportion of newly establishied clinics has increased gradually, so that they amount to 13% of the total medical facilities in Korea. Meanwhile, the number of newly established medium-size hospitals and general hospitals have decreased. The number of newly established clinics per 100, 000 populations has increased in the all areas, but the rate of increase has decreased in the cities except in 6 major cities in 1990. The rate of increase in newly established clinics surpasses that of population increase. This study has identified the trend of young physicians' early driving into their solo medical practice than before. This indicates chance of the medical specialty training nowadays toughen due to the limited openings in residency programs. However, the sex ratio of physicians at newly established clinics has not changed. The decreasing tendency to open medical practice without beds and the increasing size of clinics are found in this study(The size has been measured in terms of medical manpower, of beds, and of medical equipment in this study). Two thirds of general practitioners have opened their clinics without beds, although such trend has been less in the case of specialists. All three indicators show increasing size, especially in the case of rural clinics. However, among them, the number of medical equipments has increased most significantly from 8.9 items in 1981 to 12.9 in 1990.
Delivery of Health Care
;
General Practitioners
;
Hospitals, General
;
Humans
;
Insurance
;
Internship and Residency
;
Korea*
;
Sex Ratio
;
Specialization
2.Clinical Analysis of C.N.S. Cysticercosis.
Soo Ho CHO ; Choong Bae MOON ; Byung Yon CHOI
Yeungnam University Journal of Medicine 1984;1(1):25-34
During last 10 years we experienced 25 cases of C.N.S. cysticercosis. Now clinical analysis and evaluation of our cases were made and the results are followings; 1. Prevalence in man and women are nearly same and about 70% of cases are distributed between 20-50 years old. 2. According to Nieto's classification, mostly are ventricular (44%) and parenchymal type (36%). 3. Clinical manifestations were IICP (92%), focal neurological deficits (68%), seizure (48%), altered mental status (36%) and others listed on table 7. 4. In ventricular type, IICP and cerebellar dysfunction signs were predominated but seizure and focal neurological deficits were commonly seen in parenchymal type. 5. Subcutaneous cysticercus nodules were palpated in 32% of cases. 6. Positive stool ova was observed in 29% of cases. 7. Radiologic studies revealed as followings: 16% of cases showed abnormal findings on plain film, 84% on angiography, 94% on ventriculography and 100% on computed tomography and myelography. Computed tomography looks like most helpful diagnostic method for C.N.S. cysticercosis, they usually revealed lucent cystic lesion, hydrocephalic findings and contrast enhancement. 8. Suboccipital craniectomy, craniotomy with removal of parenchymal cyst or laminectomy were done according to location and types of lesion. 72% of operated cases revealed good results and mortality was 4% of cases.
Angiography
;
Cerebellar Diseases
;
Classification
;
Craniotomy
;
Cysticercosis*
;
Cysticercus
;
Female
;
Humans
;
Laminectomy
;
Methods
;
Mortality
;
Myelography
;
Ovum
;
Prevalence
;
Seizures
3.Pineocytoma.
Choong Bae MOON ; Byung Yearn CHOI ; Soo Ho CHO
Yeungnam University Journal of Medicine 1984;1(1):153-160
The management of pineal region tumor remains controversial. This paper reports a case of pineocytoma which was attempted to improve treatment planning by the use of clinical features, computerized tomography, and markers for germ-cell tumor. A presumptive diagnosis could be made and this tumor less likely to respond to radiotherapy was subjected to primary surgery.
Diagnosis
;
Pinealoma*
;
Radiotherapy
4.Extraosseous Extradural Cervical Tuberculoma.
Soo Ho CHO ; Byung Yearn CHOI ; Choong Bae MOON
Yeungnam University Journal of Medicine 1984;1(1):135-138
A 44-year-old female with cervical cord compression signs had myelographic and computerized tomographic evidence of extradural spinal cord compression without any tuberculous bony lesion or cold abscess. At surgery, cervical spinal cord was compressed by extraosseous extradural granulomatous tissue which was histologically proved a very rare localized extradural tuberculous granuloma.
Abscess
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Adult
;
Cervical Cord
;
Female
;
Granuloma
;
Humans
;
Spinal Cord Compression
;
Tuberculoma*
5.Organized Expanding Spontaneous Intracerebral Hematoma.
Byung Yearn CHOI ; Choong Bae MOON ; Soo Ho CHO
Yeungnam University Journal of Medicine 1984;1(1):129-134
The authors report a case of massive spontaneous intracerebral hematoma in a infant, caused by bleeding from cryptic vascular malformation associated with vitamin K dependant factor deficiency. The bleeding was initiated by vitamin K dependant factor deficiency, then 3 weeks later hematoma was expanded by rebleeding from malformed vessel after PT and PTT had been returned to normal values. The well circumscribed organized old hematoma with fresh expanded bleeding component within a huge rusty colored cystic fluid cavity was recognized in operative field and pathological ground.
Hematoma*
;
Hemorrhage
;
Humans
;
Infant
;
Reference Values
;
Vascular Malformations
;
Vitamin K
6.Malignant Neuroepithelioma (Peripheral Neuroblastoma): A Case Report
Chang Uk CHOI ; Byung Joon SHIN ; Moon Yeol PARK
The Journal of the Korean Orthopaedic Association 1990;25(4):1283-1287
Malignant neuroepithelioma is a rare neoplasm arising within the peripheral nervous system and usually occurs in the lower extremities. It may involve patients in any age group and have no gender predisposition. In adolescents and adults the tumor must be distinguished from other malignant round-cell tumors. The poor prognosis and the need for aggressive, combined surgical and chemotherapeutic modalities in treating this tumor necessitate a prompt and accurate diagnosis. Authors have experienced a case of malignant neuroepithelioma developed in left sciatic nerve. The diagnosis was confirmed by CT scan, M.R.I., light and electron microscopic findings.
Adolescent
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Adult
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Diagnosis
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Humans
;
Lower Extremity
;
Neuroectodermal Tumors, Primitive, Peripheral
;
Peripheral Nervous System
;
Prognosis
;
Sciatic Nerve
;
Tomography, X-Ray Computed
7.Growth of Children with Hypochondroplasia Treated with Growth Hormone for Two Years.
Bo Ram CHOI ; Moon Young SONG ; Byung Kyu SUH ; Byung Churl LEE
Journal of Korean Society of Pediatric Endocrinology 1998;3(1):23-27
PURPOSE:Hypochondroplasia is a skeletal dysplasia characterized by poor childhood growth and an inadequate pubertal growth spurt. Final height attainment of hypochondroplasia has been reported to range between 120 and 152cm. Increased availability of growth hormone with the introduction of recombinant human growth hormone has allowed for clinical trials in a number of growth hormone sufficient children with growth problems. The purpose of this study was to assess the growth promoting effect of human growth hormone in children with hypochondroplasia. METHODS:Five patients with hypochondroplasia diagnosed by clinical and radiological findings between 1993 and 1997 at our hospital was aged 3 and 1/2 -11 and 1/2 years. Each patients continuously received human growth hormone 0.6-0.7U/Kg/week, intramuscularly or subcutaneously in 6-7 divided dose for 2 years. Standard auxologic assessment was carried out every 3 month interval in the first year after commencement of therapy and then same assessment was 6 monthly. Bone age was assessed 6 monthly using Gleurich-Pyle method. RESULTS:Mean height velocity of pretreatment and year 1 and 2 of GH treatment were 3.9+/-0.7, 6.5+/-1.8 and 5.7+/-1.5cm/year, respectively. Mean height standard deviation score for chronological age of pretreatment and year 1 and 2 of GH treatment were -2.7+/-0.3, -2.4+/-0.3 and -2.2+/-0.4, respectively. The increase in the height velocity diminishes over the subsequent year. The increment of bone age after GH treatment were same as the increments of chronological age. CONCLUSION: Short-term GH therapy increases the height velocity of children with hypochondroplasia, but the effect of GH therapy on final height remains unknown.
Child*
;
Growth Hormone*
;
Human Growth Hormone
;
Humans
8.Preimplantation Development and Apoptosis of Mouse Embryos in the Medium Containing Extracellualr Matrix.
Byung Moon KANG ; In Pyo SOHN ; Byung Mok CHUNG ; Kyoo Wan CHOI ; Myung Chan GYE
Korean Journal of Fertility and Sterility 2000;27(3):253-259
OBJECTIVE: To verify the effect of Matrigel, a ECM complex from Engelbreth-Holm-Swarm(EHS) mouse sarcoma on the preimplantation development and apoptosis of mouse fertilized eggs. METHOD: Late Pronucleus stage eggs were cultured through the blastocyst stage in the presence of Matrigel (0.5%, v/v). Characteristics of apoptosis and cell number assessed by Hoecst staining and TUNEL labeling at the blastocyst stage, respectively. RESULTS: Morphological development, number of cells per embryo was significantly increased but rate and number of TUNEL positive nuclei of the embryo were decreased in the presence of Matrigel. CONCLUSION: This result suggested that at low concentration of Matrigel improves both viability and morphological development in the preimplantation mouse embryos.
Animals
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Apoptosis*
;
Blastocyst
;
Cell Count
;
Eggs
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Embryonic Structures*
;
In Situ Nick-End Labeling
;
Mice*
;
Ovum
;
Sarcoma
;
Zygote
9.Thyroid Diseases in Childhood.
Joo Hee NA ; Jin CHOI ; Moon Young SONG ; Byung Kyu SUH ; Byung Churl LEE
Journal of Korean Society of Pediatric Endocrinology 1999;4(2):219-225
PURPOSE: Thyroid disease is the most common endocrine disease in childhood. Thyroid hormone has critical effects on growth and development, especially in childhood. We survey the prevalence, sex and age distribution, symptoms and thyroid function states of thyroid diseases in childhood. METHODS: Three hundred ninety one children who were diagnosed as having thyroid disease at department of pediatrics, St. Mary's hospital from Jan. 1987 to Dec. 1998 enrolled in this study. RESULTS: 1) The ratio between male and female patients was 1: 5.3. Age distribution was puberty, school age and infancy in their order of frequency. 2) The results of thyroid function tests showed normal function in 210 cases (53.7%), increased function in 95 cases(24.3%), and decreased function in 86 cases (22%). 3) Simple goiter, Graves disease, and chronic lymphocytic thyroiditis were the most common diseases in euthyroid, hyperthyroid, and acquired hypothyroid state, respectively. 4) The most common sign and symptom was goiter in euthyroid(100%), hyperthyroid(98.8%) and acquired hypothyroid state(96.2%). Forty of 68 cases(58.8%) with congenital hypothyroidism were detected by neonatal screening. CONCLUSION: Simple goiter, chronic lymphocytic thyroiditis and Graves disease were common acquired thyroid diseases in childhood, and goiter is the most common clinical manifestation in acquired thyroid disease. Recently, increasing number of congenital hypothyroidism was detected by neonatal screening test.
Adolescent
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Age Distribution
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Child
;
Congenital Hypothyroidism
;
Endocrine System Diseases
;
Female
;
Goiter
;
Graves Disease
;
Growth and Development
;
Hashimoto Disease
;
Humans
;
Infant, Newborn
;
Male
;
Neonatal Screening
;
Pediatrics
;
Prevalence
;
Puberty
;
Thyroid Diseases*
;
Thyroid Function Tests
;
Thyroid Gland*
10.Atypical Case of Granuloma Annulare.
Byung Kwan RO ; Moon Seop CHOI ; Byung In RO ; Chin Yo CHANG
Korean Journal of Dermatology 1982;20(2):327-334
Granuloma annulare is a benign, usually self-limited chronic dermatasia of unknown cause, charaeterized by akin colored papules that may be arranaged in an annular configuraticn. Histopathologically, it is charicterized by camplete or incomplete foeal degeneration of collagen of chronic infliammatory cells. The authors obaerved an atypical case of granuloma annulare in a 4-year-old girl. She showed multiple papules and nodule on hands and feet. On inital examination, her skin lesions suggested histiacytosis, xanthanulama, rheumatoid nodule, or benign skin tumor. But the skin biopey revealed typica1 findings of granuloma awulare. Focal degeneration of colagen was confirmed by toluictine blue stain. Her skin lesions were almoatly cleared by skin biopsy and intralesional injectian of corticosteroid.
Biopsy
;
Child, Preschool
;
Collagen
;
Female
;
Foot
;
Granuloma Annulare*
;
Granuloma*
;
Hand
;
Humans
;
Rheumatoid Nodule
;
Skin