1.A Study on Scoliosis Induced by Resection of Thoracic Spinal Nerves
Se Hyun CHO ; In Ho CHOI ; Sang Hoon LEE ; Se Il SUK ; Sang Gweon ROE
The Journal of the Korean Orthopaedic Association 1987;22(6):1416-1426
Msny clinical and experimental studies trying to elucidate the cause of idiopathic scoliosis have been carried out. There, however, is no established theory to explain it. This paper is aimed at approaching one of various causes of idiopathic scoliosis by producing thoracic scoliosis in growing rabbits with unilateral resection of thoracic spinal nerves. All 43 rabbits were divided into four different groups. The first group(11 rabbits) consisted of rsbbits whose primary anterior and posterior divisions of the unilateral thoracic spinal nerves were resected. The second(11 rabbits) and the third(11 rabbits) were groups of rabbits whose primary anterior and posterior devisions were resected respectively. The fourth(10 rabbits) was the control group. The first group of rsbbits showed the most prominent curvature of the spine. The group of resection of primary posterior division showed less severe scoliosis than the first group but more marked scoliosis than the group of resection of primary anterior division. The biopsy of the denervated muscles included in the scoliosis revealed atrophy. It is concluded from the animal experiments with 43 growing rabbits that unilateral paralysis of the thoracic spinal nerves could be one csuse of iniopathic scoliosis and the primary posterior division of the thoracic spinal nerve contributed to the production of scoliosis more than the primary anterior division.
Animal Experimentation
;
Atrophy
;
Biopsy
;
Muscles
;
Paralysis
;
Rabbits
;
Scoliosis
;
Spinal Nerves
;
Spine
2.W-Shaped Triple V-Y Advancement Flaps for the Correction of Secondary Cleft Lip Nasal Deformity.
Woo Sung CHO ; Se Won OH ; Jin Sik BURM ; Chul Hoon CHUNG ; Suk Joon OH
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(4):575-581
A secondary cleft lip nasal deformity can be corrected by many procedures including central lip tissue transfer, forked flap, nasal floor and alar base advancement, nasal skin flaps and composite graft. These procedures have been applied for many years, but each one has some conspicuous residual problems. We propose triple V-Y advancement flaps, which we have performed on 13 secondary cleft lip and nasal deformity patients over the past 6 years. The W-shaped triple reverse V-shaped incision easily exposed the alar cartilages. We made the advancement and rotation of the nasal skin flap to lengthen the columella and project the nasal tip. Postoperatively, the columella length and nasolabial angle were found to be increased by an average of 3.7 mm and 42 degrees, respectively. In lateral view, a relatively natural nasal line was achieved. The scar in the nasal tip posed few problems. This procedure should be useful for the correction of the secondary cleft lip nasal deformity.
Cartilage
;
Cicatrix
;
Cleft Lip*
;
Congenital Abnormalities*
;
Humans
;
Lip
;
Skin
;
Transplants
3.A Case of Acute Dystonia Induced by Aripiprazole in a Patient with Tic Disorder.
Korean Journal of Psychopharmacology 2008;19(2):101-105
An 8-year-old female with Tourette Disorder (TD) was treated with a daily oral dosage of 5 mg of aripiprazole, which did not significantly improve her symptoms. After treatment with 10 mg daily for 3 days, she experienced an acute episode of dystonia with facial muscle spasms, opisthotonus, and torticolis. All symptoms resolved after ingestion of a total of 2 mg of benztropine over 2 days. Previously, aripiprazole was considered to cause few anticholinrgic, antiadrenaline, or antihistamine effects or extrapyramidal symptoms. However, extrapyramidal symptoms have now been reported in patients with TD and in adolescent patients with other psychiatric disorders. We reviewed the literature, and to the best of our knowledge, this is the first report of a child TD patient with acute dystonia. Although the recommended treatment largely precludes acute dystonic reaction, aripiprazole has produced this reaction.
Adolescent
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Benztropine
;
Child
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Dystonia
;
Eating
;
Facial Muscles
;
Female
;
Humans
;
Piperazines
;
Quinolones
;
Spasm
;
Tic Disorders
;
Tics
;
Tourette Syndrome
;
Aripiprazole
4.Expression Pattern and Prognostic Correlation of BAG - 1 Protein in Breast Cancer.
Se Hoon CHO ; Dae Young LEE ; Byung Jin KIM ; Sook Hee HONG
Journal of the Korean Cancer Association 2000;32(1):60-67
PURPOSE: The objective of this study was to understand the expression of BAG-1 in the human breast cancer. MATERIALS AND METHODS: We studied its expression in one hundred and thirteen patients diagnosed with breast cancer in Dong-A university hospital between 1992 and 1996 by performing immunohistochemical staining with BAG-1 monoclonal antibody. RESULTS: Of the 113 breast carcinoma examined, 62.0% were positive for BAG-1 cyto- plasmic expression, 28.0% were positive for nuclear BAG-1 expression and 9.7% were positive for both BAG-1 cytoplasmic and nuclear expression. The higher histologic grade was correlated with the higher cytoplasmic expression (p<0.05). Except for histologic grade, no correlation was observed between BAG-1 expression and conventional prognostic factors such as age, menopausal status, metastatic status of the axillary lymh nodes, cathepsin-D, p53, C-erbB-2, DNA ploidy, S-phase fraction, PCNA (proliferating cell nuclear antigen). CONCLUSION: The high histologic grade was found to correlate with positive BAG-1 cyto- plasmic staining which did not correlate with conventional prognostic factors. Our data indicate that furthermore investigation is warranted to define the role of BAG-1 as an meaningful prognostic factor in patients with newly diagnosed breast cancer.
Breast Neoplasms*
;
Breast*
;
Cytoplasm
;
DNA
;
Humans
;
Ploidies
;
Proliferating Cell Nuclear Antigen
5.Leser-Trelat Sign in Glioblastoma Multiforme.
Sung Bin CHO ; Mi Ryung ROH ; Jeanne JUNG ; Se Hoon KIM ; Kee Yang CHUNG
Annals of Dermatology 2005;17(2):62-64
No abstract available.
Glioblastoma*
;
Keratosis, Seborrheic
6.Williams Syndrome in an Infant An autopsy case report .
Jeong Hae KIE ; Se Hoon KIM ; Jae Young CHOI ; Sang Ho CHO
Korean Journal of Pathology 1999;33(11):1090-1093
Williams syndrome is a congenital disorder characterized by mental retardation, loquacious personalities, dysmorphic face, and vascular and valvular abnormalities. The etiology of this syndrome was one allelic loss of elastin gene, exhibiting a submicroscopic deletion, at 7q11.23. Sudden death is an infrequently recognized complication. The mechanism of sudden death is explained by myocardial ischemia, decreased cardiac output, and arrhythmia by anatomical abnormality of coronary artery stenosis and severe biventricular outflow tract obstruction. We report an autopsy case of a 80 day-old male with Williams syndrome. Five days before admission, cardiac murmur was detected incidentally on ascultation at a local clinic during a visit for vaccination. He was transferred to our hospital and cardiac catheterization was done. He died suddenly next day. Postmortem examination revealed a dysmorphic face and multiple cardiovascular abnormalities including supravalvular aortic stenosis with narrowed coronary artery ostia, supravalvular pulmonic stenosis, secundum type of atrial septal defect, right ventricular hypertrophy, and renal artery stenosis. Histologically, aorta and pulmonary, bronchial, and renal arteries showed markedly hyperplastic medial elastic laminae approximately three times thick compared to those of age-matched normal artery. The elastic fibers of the innermost two thirds of media were disposed in a normal orderly parallel fashion. In outer third of the media, the elastic fibers had lost the normal orderly arrangement.
Aorta
;
Aortic Stenosis, Supravalvular
;
Arrhythmias, Cardiac
;
Arteries
;
Autopsy*
;
Cardiac Catheterization
;
Cardiac Catheters
;
Cardiac Output
;
Cardiovascular Abnormalities
;
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
;
Coronary Stenosis
;
Coronary Vessels
;
Death, Sudden
;
Elastic Tissue
;
Elastin
;
Heart Murmurs
;
Heart Septal Defects, Atrial
;
Humans
;
Hypertrophy, Right Ventricular
;
Infant*
;
Intellectual Disability
;
Loss of Heterozygosity
;
Male
;
Myocardial Ischemia
;
Pulmonary Valve Stenosis
;
Renal Artery
;
Renal Artery Obstruction
;
Vaccination
;
Williams Syndrome*
7.Williams Syndrome in an Infant An autopsy case report .
Jeong Hae KIE ; Se Hoon KIM ; Jae Young CHOI ; Sang Ho CHO
Korean Journal of Pathology 1999;33(11):1090-1093
Williams syndrome is a congenital disorder characterized by mental retardation, loquacious personalities, dysmorphic face, and vascular and valvular abnormalities. The etiology of this syndrome was one allelic loss of elastin gene, exhibiting a submicroscopic deletion, at 7q11.23. Sudden death is an infrequently recognized complication. The mechanism of sudden death is explained by myocardial ischemia, decreased cardiac output, and arrhythmia by anatomical abnormality of coronary artery stenosis and severe biventricular outflow tract obstruction. We report an autopsy case of a 80 day-old male with Williams syndrome. Five days before admission, cardiac murmur was detected incidentally on ascultation at a local clinic during a visit for vaccination. He was transferred to our hospital and cardiac catheterization was done. He died suddenly next day. Postmortem examination revealed a dysmorphic face and multiple cardiovascular abnormalities including supravalvular aortic stenosis with narrowed coronary artery ostia, supravalvular pulmonic stenosis, secundum type of atrial septal defect, right ventricular hypertrophy, and renal artery stenosis. Histologically, aorta and pulmonary, bronchial, and renal arteries showed markedly hyperplastic medial elastic laminae approximately three times thick compared to those of age-matched normal artery. The elastic fibers of the innermost two thirds of media were disposed in a normal orderly parallel fashion. In outer third of the media, the elastic fibers had lost the normal orderly arrangement.
Aorta
;
Aortic Stenosis, Supravalvular
;
Arrhythmias, Cardiac
;
Arteries
;
Autopsy*
;
Cardiac Catheterization
;
Cardiac Catheters
;
Cardiac Output
;
Cardiovascular Abnormalities
;
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
;
Coronary Stenosis
;
Coronary Vessels
;
Death, Sudden
;
Elastic Tissue
;
Elastin
;
Heart Murmurs
;
Heart Septal Defects, Atrial
;
Humans
;
Hypertrophy, Right Ventricular
;
Infant*
;
Intellectual Disability
;
Loss of Heterozygosity
;
Male
;
Myocardial Ischemia
;
Pulmonary Valve Stenosis
;
Renal Artery
;
Renal Artery Obstruction
;
Vaccination
;
Williams Syndrome*
10.A Rare Cause of Acute Scrotal Pain: Spontaneous Thrombosis of Testicular Vein
Journal of the Korean Radiological Society 2018;79(5):282-285
Acute scrotal pain is a common clinical symptom of urinary system and there are various causes. Among them, thrombosis of testicular vein is rare, but one of the causes of acute scrotal pain. Thrombosis is a common disease that can occur anywhere in our body. But thrombosis of testicular vein has not been reported in Korea. We report a case of thrombosis of testicular vein in a 26-years-old man with acute scrotal pain.