1.Arterial embolization as the management of massive hemoptysis.
Jeong Seong KANG ; Byung Hak JUNG ; Kyoo Hye CHO ; Keun CHANG ; Eun Taik JEONG ; Byung Suk ROH
Tuberculosis and Respiratory Diseases 1993;40(2):165-170
No abstract available.
Hemoptysis*
2.Effects of corticosteroid on the paraquat induced lung injury.
Keun CHANG ; An Myung KIM ; Jeong Seong KANG ; Byung Hak JUNG ; Eun Taik JEONG ; Hyung Bae MOON
Tuberculosis and Respiratory Diseases 1992;39(4):325-333
No abstract available.
Lung Injury*
;
Lung*
;
Paraquat*
3.Splenectomy in Hereditary Spherocytosis in Childhood.
Young Soo HEO ; Chang Sig KIM ; Byung Soo DO ; Bo Yang SUH ; Jeong Ok HAH
Yeungnam University Journal of Medicine 1994;11(1):42-48
Among the erythrocyte membrane defects, hereditary spherocytosis is the most common. The erythrocyte membrane defect results from a deficiency of spectrin, the most important structural protein in red cell. Hereditary spherocytosis often presents with hemolytic anemia, jaundice, moderate splenomegaly. Diagnosis is established by the presence of spherocytes in the peripheral blood, reticulocytosis, an increased osmotic fragility, and a negative Coombs test. In children, splenectomy is usually performed after age 6 years but can be done at a younger age if warranted by the severity of the anemia and the need for frequent transfusions. In the period December 1987 to Agust 1993, 9 patients with hereditrary spherocytosis underwent splenectomy and the following results were obtained. 1. Nine patients were comprised of five males and four females. 2. Five patients(55.6%) had been admitted to our hospital during age 6-10 years. 3. Four of the nine patients had autosomal dominant inheritance with variable expression. The other five patients had no known inheritance. 4. The diagnosis of the spherocytosis was based on the increased osmotic fragility and increased autohemolysis of the erythrocytes, as well as on the appearance of spherocytes in the peripheral blood smear. 5. In all cases splenectomy was performed. Two patients had concomitant gall stones and choledocholithiasis, respectively. One patient with concomitant gall stones underwent simultaneous cholecystectomy and splenectomy. The other patients associated with choledocholithiasis underwent splenectomy, cholecystectomy, choledocholithotomy, and T-tube drainage. 6. Complete hematologic recovery was obtained by the splenectomy in all cases. 7. Postoperative complication was not occurred.
Anemia
;
Anemia, Hemolytic
;
Child
;
Cholecystectomy
;
Choledocholithiasis
;
Coombs Test
;
Diagnosis
;
Drainage
;
Erythrocyte Membrane
;
Erythrocytes
;
Female
;
Gallstones
;
Humans
;
Jaundice
;
Male
;
Osmotic Fragility
;
Postoperative Complications
;
Reticulocytosis
;
Spectrin
;
Spherocytes
;
Splenectomy*
;
Splenomegaly
;
Wills
4.Spinal Muscular Atrophy Type 2 in Siblings.
Jeong Sam JEON ; Dong Hub LEE ; Byung Soo CHO ; Sa Jun CHUNG ; Chang Il AHN
Journal of the Korean Pediatric Society 1989;32(5):718-723
No abstract available.
Muscular Atrophy, Spinal*
;
Spinal Muscular Atrophies of Childhood*
5.Clinical study of pregnancy success on peritoneal oocyte and sperm transfer.
Sang Hoon LEE ; Byung Joon CHEONG ; Hyun Jeong CHANG ; Do Hwan BAE
Korean Journal of Obstetrics and Gynecology 1991;34(11):1535-1543
No abstract available.
Oocytes*
;
Pregnancy*
;
Spermatozoa*
7.Pyogenic Arthritis in Renal Transplant Recipients.
Jung Man KIM ; Chang Whan HAN ; Jeong Tae SEO ; Byung Kee BANG ; Yong Bok KOH
The Journal of the Korean Orthopaedic Association 1997;32(3):689-696
Acute pyogenic arthritis in renal transplant patient is one of the serious problem resulting in significant morbidity and mortality. The purpose of this paper is to analyze seven patients in whom acute pyogenic arthritis developed following renal transplantation. Pyogenic arthritis developed in seven (0.7%) out of 958 renal transplant patients whose transplanted kidney functioned well for more than two years. The age of the patients ranged from 37 to 65 years with a mean of 48 years. All patients were male. Pyogenic arthritis developed between the period of one and 12 years (mean: 4.5+/-4.2 years) following transplantation. Causative organisms were Staphylococcus aureus (three), E. coli (two), Salmonella (one) and Acinetobacter bananii (one). Involved joints were four knees, one hip, one elbow and one finger. Two patients improved on a conservative regimen of bed rest and antibiotics and five patients required open drainage. However, pyogenic arthritis recurred in three years, four years and seven years after renal transplant in one patient. Looking at the probable risk factors of age, sex, immunosuppresants, diabetics and acute graft rejection, diabetics and older age (over 40 years old) are highly associated with post renal transplant pyogenic arthritis.
Acinetobacter
;
Anti-Bacterial Agents
;
Arthritis*
;
Bed Rest
;
Drainage
;
Elbow
;
Fingers
;
Graft Rejection
;
Hip
;
Humans
;
Joints
;
Kidney
;
Kidney Transplantation
;
Knee
;
Male
;
Mortality
;
Risk Factors
;
Salmonella
;
Staphylococcus aureus
;
Transplantation*
8.Slipped Capital Femoral Epiphysis: Reports of Two Cases
Yon Il KIM ; Soo Kyoon RAH ; Chang Uk CHOI ; Byung Il LEE ; Seog Yeong JEONG
The Journal of the Korean Orthopaedic Association 1987;22(3):819-824
The slipped capital femoral epiphysis is characterized by a growth disturbance of the capital physi. resulting in weakening of this structure and a subsequent displacement of the femoral head on the fe moral neck. It is a rare entity in Korea and only six cases have been reported so far1-5). One of ou cases was a bilateral mild acute slips in 13 yearold boy which were treated by Hagie pinning. Th other case, a 17 year-old boy, who suffered from a moderate acute on chronic slip in his left hip an showed a typical Pistol grip deformity. He was treated by gentle closed rcduction and Knowles pi fixation with good result.
Congenital Abnormalities
;
Epiphyses
;
Hand Strength
;
Head
;
Hip
;
Humans
;
Korea
;
Male
;
Neck
;
Slipped Capital Femoral Epiphyses
9.Multiple Myelographic Defects at Lumbosacral Region and Appropriate Area of Operation
Yon Il KIM ; Soo Kyoon RAH ; Chang Uk CHOI ; Byung Il LEE ; Seog Yeong JEONG
The Journal of the Korean Orthopaedic Association 1988;23(1):193-203
When the multiple myelographic defects at lumbosacral region are noted, the prudential effort for decision of appropriate area of surgical decompression would be needed. Fifty four patients who had been treated surgically for the deseases, such as HNP and spinal stenosis, from March in 1982 to Feb. In 1987 at Department of Orthopecdic Surgery, Soonchunhyang University Hospital, were analyzed in order to define the etiology, the level of the defect, indication for the operation and to assess the results of each level which had been operated. The results of the study were as follows. 1. The number of patients, which the multiple indentations were noted in the myelogrsphy, was 54 cases, 29 spinal stenosis, 15 HNP and 10 mixed types. 2. The most common defect levels in myelography were L3-4 snd L4-5, which were 19 cases (35.2%), the next levels were L4-5 and L5S1, which were 16 cases(29.6%), then L3-4, L4-5 and L5S1 were 7 cases(13%) and the other levels were 12 cases(22.2%). 3. The decision for the sppropriste operation area had not be done following to the size of the myelographic defect, but the clinical symptoms and physicsl exsminations. 4. The results were classified ss excellent or good in 79.7%, which was 80% at two levels snd 79.5% at one level. 5. The operation levels could be decressed for the reducing the spinal instability, operation time and possibility of the dangerous conditions and promotion of early restoration and, ambulation, if the severe differences between the results of one and two operation levels were not seen.
Decompression, Surgical
;
Humans
;
Lumbosacral Region
;
Myelography
;
Spinal Stenosis
;
Walking
10.Relationship between s-phase fraction and survival time in patients with primary squamous lung cancer.
Byung Hak JUNG ; Jeong Seong KANG ; Keun CHANG ; Eun Taik JEONG ; Hun Taeg CHUNG ; Hyung Bae MOON
Tuberculosis and Respiratory Diseases 1993;40(6):669-676
No abstract available.
Humans
;
Lung Neoplasms*
;
Lung*