1.A Case of Monilethrix.
Korean Journal of Dermatology 1979;17(5):361-365
Monilethrix is a rare hereditary disorder of hair first described by Walter G. Smith in 1879, and usually transmitted as autosomal dominant trait. It is characterized hy bead like enlargement af the affected hair, alapecia resulting from ha.ir breakage and keratosis pila.l is. This 3 year old female child patient has been suffered from easy destrurtion of beaded scalp hair and follicular hyperkeratosis of the occipital region since infancy. Past hiatory was ncecontributory and the pe,digree of family showed autosomal dominant trait. Physical examinatior was not rernarkable except skin lesian and laboratory findings were within normal limit. Microscopic finding of the affected hair showed alternating constrictians and node. The scalp bivpsy findings showed mild hyperkeratosis, keratotic plug, mild cellular infiltration of papillary derrnia and perifollicular area.
Child
;
Child, Preschool
;
Female
;
Hair
;
Humans
;
Keratosis
;
Monilethrix*
;
Scalp
;
Skin
2.Irreducible Dorsal Dislocation of First Metatarsophalangeal Joint by Closed Method: Report of a Case
Jin Hyok KIM ; Kyoo Ho SHIN ; Byung Jik KIM
The Journal of the Korean Orthopaedic Association 1988;23(4):1201-1204
Traumatic dislocation of the first metatarso-phalangeal joint is rare injury. The mechanism of this injury is hyperextension of the great toe, causing displacement of the proximal phalanx on the dorsum of the first metatarsal head and neck. The complex soft tissue anatomy surrounding this joint interferes with the closed reduction of the dislocation. This paper describes a patient with complete dorsal dislocation of the first metatarsophalangeal joint treated at the Paik hospital which cannot be reduced by closed manipulation.
Dislocations
;
Head
;
Humans
;
Joints
;
Metatarsal Bones
;
Metatarsophalangeal Joint
;
Methods
;
Neck
;
Toes
3.A Case fo Elephantiasis Neuromatosa.
Shin Kyoo KIM ; Tae Jin KIM ; Soon Kyoon YANG ; Jin Tack KIM
Korean Journal of Dermatology 1980;18(6):613-617
Elephantiasis neuromatosa is one of 3 types of cutaneous tumors in Von Recklinghausen's disease. This 28 year-old male patient visited for adult-fist sized tumor associated with hairy pigmented patch on right antecubital fossa, and various sized tumors and cafe-au-lait spots on whole body of about 27 years duration. Past history was noncontributory. Family history revealed that his father and son had similar manifestations. Laboratory findings were noncontributory. Histopathology of cafe-au-lait spot and hairy pigmented patch revealed increase of melain in basal cell layer of the epidermis and increase in the concentratiton and activity of the melanocytes in basal cell layer of the epidermis. Histopathology of the mass revealed slightly thin, wavy fibrs lying in loosely textured strands extending in varying directions and a fairly large number of nuclei that are ovel to spindle-shaped and fairly uniform in size.
Adult
;
Cafe-au-Lait Spots
;
Deception
;
Elephantiasis*
;
Epidermis
;
Fathers
;
Humans
;
Male
;
Melanocytes
;
Neurofibromatosis 1
4.A Case of Tuberous Sclerosis Associated with Abnormal EEG.
Shin Kyoo KIM ; Sung Ho CHO ; Soon Kyoon YANG ; Jin Tack KIM
Korean Journal of Dermatology 1980;18(2):133-139
Tuberous Sclrosis is a rare hereditary disease first described by Bourneville in 1880, and usually transmitted as autosomal dominant trait, and is characterized by mental retardation, seizares, and adenoma sebaceum. This 21 year old male patient visited for multiple pin head to pea siaed yelhwish red waxy papules on the face and gingival papillema af 10 years dunatio. Attacks of grandmal seisure eccr oacurred times in the past 8 yeara. Past hiatory and family history were noncountributory. There was a shagreen patch on left lower lumbo-sacral area. Hiatopathology disclosed an adenoma sebaceum showing dilatation of the capillaries, proliferation of collagen, mild cellular infiltration of papillary dermis and perivascular areas. EEG revealed asymmetrieal slow waves on right side of the brain, predommantly in anterior part, and intermittent sharp waves on right anterior frontotemporal area of the brain.
Brain
;
Capillaries
;
Collagen
;
Dermis
;
Dilatation
;
Electroencephalography*
;
Genetic Diseases, Inborn
;
Head
;
Humans
;
Intellectual Disability
;
Male
;
Peas
;
Tuberous Sclerosis*
;
Young Adult
5.Comparison of Propofol-N2O and Propofol-fentanyl Anesthesia for Outpatient Surgery.
Jin Yun KIM ; Kyung Joong KIM ; Eun Gil RAH ; Sun Kyoo PARK
Korean Journal of Anesthesiology 1997;33(3):441-446
BACKGROUND: The choice of anesthetic agents and adjuvants during outpatient surgery is of critical importance. Propofol is widely used for the induction and maintenance of outpatient anesthesia. Because propofol lacks analgesic properties, very high concentrations may be required when propofol is used as the sole anesthetic drug. Propofol is used with adjuvants such as nitrous oxide or opioid. This study was designed to evaluate the intraoperative hemodynamic response, recovery characteristics and side effects of propofol-fentanyl anesthesia compared with propofol-N2O anesthesia for outpatient surgery. METHODS: Twenty six healthy and unpremedicated patients scheduled for outpatient surgery were randomly allocated to receive either propofol-N2O anesthesia (N-group) or propofol-fentanyl anesthsia (F-group). The patients in N-group were ventilated with nitrous oxide 60~70% in oxygen and the patients in F-group were ventilated with oxygen 40% in nitrogen via laryngeal mask airway (LMA). RESULTS: There was no significant difference in blood pressure during anesthesia, recovery time and side effects between two group. There was significant decrease of heart rate in F-group. CONCLUSION: We concluded that nitrous oxide and fentanyl are reasonable adjuvants of propofol anesthesia in outpatient anesthesia.
Ambulatory Surgical Procedures*
;
Anesthesia*
;
Anesthetics
;
Blood Pressure
;
Fentanyl
;
Heart Rate
;
Hemodynamics
;
Humans
;
Laryngeal Masks
;
Nitrogen
;
Nitrous Oxide
;
Outpatients*
;
Oxygen
;
Propofol
6.Benign osteoblastoma of the mandible: report of a case and review of the literature.
Kyoo Sik KIM ; Myung Jin KIM ; Byoung Moo SEO ; Seong Chai CHU ; Gi Cheol LEE
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1991;17(4):54-60
No abstract available.
Mandible*
;
Osteoblastoma*
7.Benign osteoblastoma of the mandible: report of a case and review of the literature.
Kyoo Sik KIM ; Myung Jin KIM ; Byoung Moo SEO ; Seong Chai CHU ; Gi Cheol LEE
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1991;17(4):54-60
No abstract available.
Mandible*
;
Osteoblastoma*
8.A Clinical Analysis of the Scapula Fractures
Jin Hyok KIM ; Kyoo Ho SHIN ; Byung Jik KIM ; Kwang Yoon SEO
The Journal of the Korean Orthopaedic Association 1988;23(4):1027-1030
Fracture of the scapuls is one of the rare bony injuries seen in hospital practice. Authors reviewed the records and the roentgenograms of forty three patients from April 1976 to March 1987. The results were as follows : l. Of the 43 cases, peak incidence was in the middle aged men with high activity, and age range was 30 to 50 years. 2. The most common cause of injury was the motor vehicle accident. 3. Twenty eight cases of the scapular fracture occurred in the body, and eleven had fractures more than two parts in the scapuls. The most common type was the combined fracture of the body and neck. 4. A severe force was required to produce the injury and 79% of the patients had combined injuries of head and chest. 5. Delay in diagnosis was frequent because of the masking effect of the associated injury. 6. Although results of conservative measurements on the scapular fracture are generally good, we feel that treatment on more active line should be undertaken in young and active patients with fracture involving glenoid.
Diagnosis
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Head
;
Humans
;
Incidence
;
Male
;
Masks
;
Middle Aged
;
Motor Vehicles
;
Neck
;
Scapula
;
Thorax
9.A Case of Xanthogranuloma on Scalp in Adult.
Young Il CHUN ; Shin Kyoo KIM ; Kyu Joong AHN ; Young Jin OH ; Yoo Shin LEE
Korean Journal of Dermatology 1985;23(3):408-410
Juvenile xanthogranuloma is characterized by one, or oftener many, yellow, re3dish yellow, or, brown 4-to-20 mm papules or nodules on the face, scalp, trunk, and mostly, extensor surfaces. It may involve internal organ besides the skin such as eye, gastrointestinal and genitourinary tracts. anthogranuloma in adult is usually solitary and dose not involve organs other than skin, and generally dose ncit resolve without treatment. Histopathologically, characteristic Touton giant cells usually appear numerously. We report a case of juvenile xanthogranulorna which occured on scalp of 49 year-old male showing typical clinical and histopathological findings.
Adult*
;
Giant Cells
;
Humans
;
Male
;
Middle Aged
;
Scalp*
;
Skin
;
Xanthogranuloma, Juvenile
10.A clinical analysis of 80 renal transplantation.
Hyung Kyoo KIM ; Joon Hun JUNG ; Il Dong JUNG ; Kyung Ho SEO ; Jin Min KONG
The Journal of the Korean Society for Transplantation 1993;7(1):107-117
No abstract available.
Kidney Transplantation*