1.A Case of Infectious Mononucleosis with Fever and Cervical Lymphadenopathy.
Journal of the Korean Medical Association 1998;41(9):978-980
No abstract available.
Fever*
;
Infectious Mononucleosis*
;
Lymphatic Diseases*
2.Clinical Study with Descresept(R).
Korean Journal of Dermatology 1976;14(2):97-100
The 16 out of 19 cases with combined oral administration oral of Descrespet and Tetracycline hydrochloride were considerably more effective in treatment of severe acne than Tetracycline hydrochloride alone or placebo in this study. 10 cases of atopic dermatitis and 6 severe acne with side effect for tetracycline hydrochlorid, such as aMominal discomfortness, also treated with Descresapt: 7 cases of atopic dermatitis and 4 acne cleared definitely faster than in patient not given Descresept Conclusively, it is cnosidered that the Descresept is effective in the tretment of severe acne and atopic dermatitis.
Acne Vulgaris
;
Administration, Oral
;
Dermatitis, Atopic
;
Humans
;
Tetracycline
3.A Case ofFamilial Benign Chronic Pemphigus.
Korean Journal of Dermatology 1974;12(4):245-248
A case of familiar benign chronic pemphigus is reported. A 41 years old housewife has recurrent history of developing grouped vesicular eruptions with erythematous erosion on the intertrigenous area since 29 years of her age. The lesions were used to aggrevated in summer and improved in autumn. Familiar history revealed same disease of her grand mother, father, 44 year old elder sister and 39 year old younger sister. All of whom had similar clinical signs and symptoms. Routine physical and laboratoryfindings were within normal limits. The histopathological findings, from vesicular eruption of the lateral aspect of neck, showed multilocular suprabasal clefts with acantholsis, villi formation and hyperkeratosis. The lesions were-improved hy the local application of corticosteroidoid ointment only.
Adult
;
Fathers
;
Humans
;
Mothers
;
Neck
;
Pemphigus, Benign Familial*
;
Siblings
4.A Case of Hereditary Anhidrotic Ectodermal Dysplasia.
Korean Journal of Dermatology 1973;11(2):69-72
A case of hereditary anhidrotic ectodermal dysplasia associated with atopic dermatitis in 16 month old male is reported. He has been suffered from multiple symptoms of anhidrosis, hypotrichosis, anodontia and atopic dermatitis. The skin showed pale, shiny, thin and dry and hairless on whole body except in the scalp. Without sweat gland and flattening of epidermis on skin biopey is compatible with an hereditary anhidrotic ectodermal dysplasia.
Anodontia
;
Dermatitis, Atopic
;
Ectodermal Dysplasia*
;
Epidermis
;
Humans
;
Hypohidrosis
;
Hypotrichosis
;
Infant
;
Male
;
Scalp
;
Skin
;
Sweat Glands
5.A Case of the Primary Malignant Melanoma in Conjunctiva.
Journal of the Korean Ophthalmological Society 1969;10(4):19-21
Malignant melanoma is considered as one of the tumor originated from precancerous melanosis and predilected in the iris and choroid. The Authors experienced a case of malignant melanoma affecting the upper palpebral conjunctiva in 39 year old female. The tumor mass was excised radically and followed by X-Ray therapy. Slight opacities of lens body is developed after X-ray irradiation.
Adult
;
Choroid
;
Conjunctiva*
;
Female
;
Humans
;
Iris
;
Melanoma*
;
Melanosis
;
X-Ray Therapy
6.The clinical analysis of choledochal cyst.
Seok Won CHIM ; Young Joo LEE ; Won Jin CHOI
Journal of the Korean Surgical Society 1993;45(4):527-535
No abstract available.
Choledochal Cyst*
7.The Metabolic Acidosis and Clinical Outcome in Acute Infantile Diarrhea.
Kee Hwan YOO ; Joo won LEE ; Soon Kyun KIM
Journal of the Korean Pediatric Society 1994;37(3):332-338
To determine the types of metabolic a cidosis using anion gap in acute infantile diarrhea and to correlate it with clinical outcome, we examined 103 infants admitted with acute diarrhea. The serum electrolytes (sodium, potassium, chloride, phosphorus), creatinine, CO2 content and anion gap were measued on first admission day. They were classified group A with normal anion gap (8~16mEq/L) and group B with increased anion gap (>16mEq/L). The results were as follows. 1) The number of group A with normal anion gap (11.6+/-3.3mEq/L) was 62 and the number of group B with incresed anion gap(21.1+/-5.5mEq/L) was 38. 2) The duration of diarrhea was significantly prolonged in group B (9.0+/-2.5 days), compared with group A (5.9+/-1.1 days)(p<0.001). 3) The duration of admission was significantly prolonged in group B(5.6+/-2.2 days), compared with group A (4.+/-01.4days)(p<0.001). 4) Infants in group B, compared with group A, were significantly more severe dehydrated (p.
Acid-Base Equilibrium
;
Acidosis*
;
Creatinine
;
Diarrhea
;
Diarrhea, Infantile*
;
Electrolytes
;
Humans
;
Infant
;
Potassium
8.Benign Fibrous Histiocytoma of Spinal Cord.
Hae Joo NAM ; Won Hee CHOI ; Tae Sook LEE
Korean Journal of Pathology 1988;22(4):510-514
Fibrous histiocytoma composed of fibroblasts and histiocytes is quite variable in histologic pattern. The biologic behavior is unpredictable by histologic ground. This tumor is well-known in subcutaneous tissue and deep soft tissue, but quite rare in central nervous system. We experienced a case of the fibrous histiocytoma involving the dura mater of spinal cord in a 26 year old female patient. In gross findings, the mass was a well demarcated, ovoid mass attached to the dura matter, and measured 2.5x1.5 cm in diameter. The cut surface was rubbery, solid, gray-white or yellow. Microscopically, the lesion consisted of polyhedral cells with round or oval nuclei and faintly eosinophilic or vaculoated cytoplasm, and multinucleated giant cells. Some giant cells were Touton-type. Composing cells were bland-looking. Mitotic figures were average 3 per 10 high power fields.
Female
;
Humans
9.Spontaneous Pneumomediastinum: Natural History and Clinical Significance.
Eun Young RUE ; Won Jae LEE ; Suk Joo RHA
Journal of the Korean Society of Emergency Medicine 1997;8(4):535-541
STUDY OBJECTIVE: We evaluate the clinical characteristics and natural history of patients presenting with spontaneous pneumomediastinum (SPNM) . DESIGN: A retrospective case series was conducted to identify patients diagnosed with SPNM. ICD-7(J98.2) discharge codes were used for Jan. 1993 to Aug. 1996 at four institutions , and emergency department(ED) records and admission charts were reviewed. Clinical features, interventions, complications, setting, etiology, symptoms, and length of hospital stay were recorded. PARTICIPANTS: All ED patients more than 12 years old with a diagnosis of SPNM. RESULTS: Thirteen cases were identified. Age range was 14 to 58 years(mean 24 years). Presenting symptoms were chest pain in eight(62%), dyspnea in six(46%), both symptoms in three(23%), no complaints in three(23%). Seven(54%) patients complained only of throat discomfort. Seven(54%) had subcutaneous emphysema, and two(15.3%) had a small pneumothorax. Two(15.3%) were smokers. Three(23%) had normal esophagograms and another three had normal chest CT findings. Two cases(15.3%) were associated with inhalational drug use and three cases were due to exercise. Nine cases(69%) had a history of "Valsalva-type" maneuver. Two patients(15%) had a history of antituberculous treatment and one(7.7.%) had suffered from bronchial asthma. Mean hospital days were 7.3 days(range 3 to 14), none of all needed any intervention. Specifically, no patient developed a subsequent pneumothorax or airway compromise. Seven cases(54%) were received prophylactic antibiotics. CONCLUSION: Most simple SPNM cases are benign disease and most of them(78%) had shown typical chest pain, dyspnea and subcutaneous emphysema. Inhalational drug use is not a main cause of SPNM yet, but increase in use of bronchoinhalers is a suspicous cause of SPNM.
Anti-Bacterial Agents
;
Asthma
;
Chest Pain
;
Child
;
Diagnosis
;
Dyspnea
;
Emergencies
;
Humans
;
Length of Stay
;
Mediastinal Emphysema*
;
Natural History*
;
Pharynx
;
Pneumothorax
;
Retrospective Studies
;
Subcutaneous Emphysema
;
Tomography, X-Ray Computed
10.Two Cases of Hyperlippoproteinemia (Type II).
Joo Bong LEE ; Byung In RO ; Chung Won KIM
Korean Journal of Dermatology 1973;11(3):197-202
Two cases of hyperlipoproteinemia is reported, Hyperlipoproteinemia is characterized by various kinds of cutaneous xanthomatosis associated with or without arteriosclerotic changes due to increasing lipoprotein fraction of the serum. Case I . 37-year old housewife had multiple, pea to nut sized, various shaped, cutaneous and subcutaneous nodular masses has been developed last 3 years. Some of her family member have similar symptoms. Serum cholesterol level was 790 mg% and serum triglyceride level was 270 mg% after 14 hour fasting. Case II. 52-year old housewife was suffered from pea sized, multiple, subcutaneous nodular and cutaneous eruptions last 2 years. There was no family histories. Serum cholesterol level was 895 mg% and serum triglyceride level was 350 mg% after 14 hour fasting. Typical Touton giant cells were found in biopsy specimens taken from cutaneous lesons. ECG, X-ray, glucose toleranc test and other laboratory examinations showed within normal limits. Tne agarose electrophoresis pattern of serum lipoprotein fractions are very similiar with that of hyperlipoproteinemia type II. These two patients were treated with nicotinic and 1. 0 gm and clofibrate 2.0 gm daily by mouth and restricted animal fatty foods. Total serum cholesterol level was markedly decreasea 2 months after treatment in case I.
Adult
;
Animals
;
Biopsy
;
Cholesterol
;
Clofibrate
;
Electrocardiography
;
Electrophoresis
;
Fasting
;
Giant Cells
;
Glucose
;
Humans
;
Hyperlipoproteinemia Type II
;
Hyperlipoproteinemias
;
Lipoproteins
;
Middle Aged
;
Mouth
;
Nuts
;
Peas
;
Sepharose
;
Triglycerides
;
Xanthomatosis