1.A Clinical Study on Intracompartmental Pressure of Leg Using Slit Catheter
Tae Hwan CHO ; Nam Jin JUNG ; Chi Jung KANG
The Journal of the Korean Orthopaedic Association 1987;22(2):478-480
Intracompartmental pressure of leg was measured by the slit catheter technique in one hundred fifty compartments of one hundred cases; fifty were from healthy young male adults, the others were from tibial fractured patients during three years from March 1983 to Fobruary 1986. The results were as follows; 1. Slit-catheter technique was found as a accurate method for continuous pressure monitoring. 2. The range of normal pressure was from zero to six millimeters of mercury(1.45mmHg±0.85). 3. Tissue pressure was 0–15mmHg(4.03mmHg±1.83) in unaffected side of fractured patients, 4–35mmHg(14.65mmHg±2.05) in affected side of fractured patients.
Adult
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Catheters
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Clinical Study
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Humans
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Leg
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Male
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Methods
2.Cystic Adventitial Disease of the Popliteal Artery: A case report.
Soo Min KANG ; Kyeong Cheon JUNG ; Je G CHI
Korean Journal of Pathology 1993;27(4):418-420
Localized cystic degeneration of peripheral arteries represents and unusual cause of arterial insufficiency. It frequently occurs in patient without generalized arteriosclerosis. It has been reported in patients from age 11 to 62 years. Cystic adventitial disease is most common in the popliteal artery. At least 115 cases have been reported worldwide, but none in Korea. We report a case of cystic adventitial disease involving the left popliteal artery. This 64-year-old man presented with an 18-month history of cramping pain of sudden onset in the left calf and claudication. Angiographic findings showed a 6 cm length of luminal obliteration of the popliteal artery. Segmentally resected popliteal artery showed two longitudinally directed cystic masses measuring 3.5x1.5 cm and 2.5x1.5 cm in the adventitia. Microscopic examination revealed cystic space in the arterial adventitia compressing arterial lumen. There were a number of foamy histiocytes collected along the cystic lumen.
Male
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Humans
3.Fatty Hamartoma of Epicardium.
Hyun Wook KANG ; Jung Ran KIM ; Jeong Wook SEO ; Je G CHI
Korean Journal of Pathology 1989;23(1):132-135
The fatty hamartoma of pericardium is characterized by abnormal accumulations of adipose tissue forming a recognizable mass. We reported a case that could best be put into "fatty hamartoma" group. This 66 year old male presented with atrial fibrillation came in for a anterior mediastinal mass. He received an operation for adenocarcinoma of ascending colon several months ago. The chest CT revealed an inhomogeneous mass in the right anterior mediastinal area, which was not clearly demarcated from the right cardiac border. The heart was deviated to the left side due to the mass. Surgical excision was performed under the impression of cardiac teratoma. The large mass was well encapsulated, and was bright yellow and partly pink, and measured 12x8 cm. Microscopically, the mass consisted predominantly of mature fat cells and abundant fibrous tissue with scattered nests of primitive cardiac muscle cells. Reviewing the literature we found the term "fatty hamartoma" could also refer to rhabdomyolipoma or fibrolipoma. Since it contains entrapped cardiac muscle cells, abundant fibrous tissue, multiple blood vessels and fetal fat cells, it could best the categorized into "hamartoma". The term "fatty" represents it's main component. Therefore we propose the term "fatty hamartoma" that could to be used further.
Male
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Humans
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Adenocarcinoma
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Hamartoma
4.Correlation among Electrocardiographic, Echocardigraphic and Hemodynamic Analysis in Atrial Septal Defect, Ostium Secundum type.
Soon Jung LEE ; Chi Han KWON ; Joon Sik KIM ; Tae Chan KWON ; Chin Moo KANG
Journal of the Korean Pediatric Society 1990;33(7):946-951
No abstract available.
Electrocardiography*
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Heart Septal Defects, Atrial*
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Hemodynamics*
5.Temporomandibular joint bony ankylosis following postoperative radiotherapy for maxillary cancer.
Yeung Joon LEE ; Chi Hee PARK ; Dae Won KANG ; Jye Jung SOH ; Jye Jynn ANN
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1993;19(4):533-539
No abstract available.
Ankylosis*
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Radiotherapy*
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Temporomandibular Joint*
6.The Carpal Angle, Metacarpal Sign and Sesamoid Index of the Healthy Koreans
Chi Jung KANG ; Snag Ho HA ; Sang Hong LEE ; Young Bai PYO
The Journal of the Korean Orthopaedic Association 1989;24(4):1260-1263
The authors estimated and analyzed the carpal angle, metacarpal sign and sesamoid index in the roentgenogram of both hands of healthy 180 male and 180 female Koreans. The results were as follows. 1. The mean value of carpal angle was 133.3°±5.8° in the right hand and 133.5°±5.1° in left hand. 2. The negative metacarpal sign were seen in 93.9 percent of normal subject. 3. The mean value of sesamoid index was 19.6±5.4 in male and 18.2±4.9 in female.
Female
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Hand
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Humans
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Male
7.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
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Humans
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Hyperlipidemias
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Hyperlipoproteinemia Type II
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Korea
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Plasma
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Xanthomatosis
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Xanthomatosis, Cerebrotendinous
8.Osteogenesis Imperfecta: Case Report
Chi Jung KANG ; Snag Ho HA ; Sang Hong LEE ; Keun Ho PARK
The Journal of the Korean Orthopaedic Association 1989;24(5):1497-1502
Osteogenesis imperfecta is a hereditary condition characterized by fragility of bone, deafness, blue sclera, laxity of joints and a tendency to improvement with age. Authors experienced osteogenesis imperfecta that develped over 3 generations in one pedigree. A 28 years old female exhibited severe anterior bowing deformity of left tibia. She has a past history of many times of bone fractures. She was treated with corrective osteotomy, plate fixation for correction of bowing deformity of left tibia and medullary nailing with fibular graft for paeudarthrosis of Rt. forearm bone.
Congenital Abnormalities
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Deafness
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Family Characteristics
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Female
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Forearm
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Fractures, Bone
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Humans
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Joints
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Osteogenesis Imperfecta
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Osteogenesis
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Osteotomy
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Pedigree
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Sclera
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Tibia
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Transplants
9.Supracondlylar Osteotomy for Cubitus Varus
Chi Jung KANG ; Snag Ho HA ; Sang Hong LEE ; Dong Min SHIN ; Jin Seok PARK
The Journal of the Korean Orthopaedic Association 1990;25(3):885-891
Cubitus varus deformity is the most common angular deformity resulted by supracondylar fractures in children. Although, this deformity rarely limit elbow function, the correction is frequently requested due to cosmetic problem. The normal carrying angle can be restored by supracondylar osteotomy. Previous reports controversy over the cause of the deformity, the necessity and timing of operative correction, the operative technique itself, and the attendant risks. We performed 18 lateral closing wedge osteotomies with French technique(10 cases), and Sherman plate fixation(8 cases) by posterolateral approach from January 1978 to December 1988 at Chosun University Hospital. The results were as follows: 1. The most common cause of cubitus varus was suprcondylar fracture of the humerus(88.9%). 2. The results of supracondylar osteotomies were excellent is 8 cases(44.8%), good in 7 cases (38.9%), poor in 3 cases(16.7%). 3. The varus and rotational deformities were corrected by modified French method and Sherman plate fixation after lateral closing osteotomy. 4. In case of plate fixation, good results were obtained even older cases because of reducing time of extermal immobilization and promotion early joint exercise.
Child
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Congenital Abnormalities
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Elbow
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Humans
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Immobilization
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Joints
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Methods
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Osteotomy
10.Dysplasia Epiphysialis Punctata: A Case Report
Hack Bong LEE ; Sang Ho HA ; Sang Keun OH ; Chi Jung KANG ; Young Chull KIM
The Journal of the Korean Orthopaedic Association 1986;21(4):709-712
Dysplasia epiphysialis punctata is a rare congenital disorder of infancy affecting in particular cartilage, muscle, jointtcapsules and the eyes. A case of dysplasia epiphysialis punctata with involvement of all epiphyses of extremities, spine and pelvis in 2 days old male is to be reported with review of literature.
Cartilage
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Chondrodysplasia Punctata
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Epiphyses
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Extremities
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Humans
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Male
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Pelvis
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Spine