1.The Relationship of Positive Antimicrosomal Antibody and Postpartum Thyroiditis.
Jin Wan PARK ; Won Ki LEE ; Eul Jong HUR ; Kyung Sim KOH ; Kwang Chul SHIN
Korean Journal of Perinatology 1998;9(3):279-284
Postpartum thyroiditis is a common but frequently unrecognized disorder, affecting approximately 5% of women during the first 12 months after delivery. It is characterized by transient hyperthyroidism occurring about 14 weeks postpartum followed by transient hypothyroidism at 19 weeks postpartum. Our aim is to investigate the prevalence of positive antimicrosomal antibody in women 3 months postpartum and an association of antimicrosomal antibody with symptomatic and biochemical thyroid disorders. We used data collected from 205 women who visited Dankook University Hospital in 3 months postpartum, Our results showed that the rate of positive antithyroid microsomal antibody was 12.7% in women 3 months postpartum and the prevalence of biochemical hyperthyroidism and biochemical hypothyroidism with positive antithyroid microsomal antibody women 3 months postpartum were 26.9% and 19.2%, respectively. The prevalence of postpartum biochemical thyroid dysfuncion 3 months postpartum was 13.7%. There was no relationship between any of the following factors and thyroid antibody status: fetal distress, birth weight and infant sex, matemal age, experiences and mode of delivery, previous medical disease(such as pstrointestinal and psychotic diseases), experiences of previous abortions, gestational age and past history of thyroid diseases.
Abortion, Induced
;
Birth Weight
;
Female
;
Fetal Distress
;
Gestational Age
;
Humans
;
Hyperthyroidism
;
Hypothyroidism
;
Infant
;
Postpartum Period*
;
Postpartum Thyroiditis*
;
Prevalence
;
Thyroid Diseases
;
Thyroid Gland
2.Clinical experiences with opalmon(OP-1206-alpha-cd, oral prostaglandin E1 preparation) in buerger's disease of lower extremities.
Yong Bok KOH ; Jang Sang PARK ; Min Kwang HONG ; In Chul KIM
Journal of the Korean Surgical Society 1993;44(6):938-953
No abstract available.
Alprostadil*
;
Lower Extremity*
;
Thromboangiitis Obliterans*
3.Clinical experience with opalmon(OP-1206-?CD, oral prostaglandin E preparation) in buerger's disease of lower extremities
Yong Bok KOH ; Jang Sang PARK ; Min Kwang HONG ; In Chul KIM
Journal of the Korean Society for Vascular Surgery 1993;9(1):42-57
No abstract available.
Lower Extremity
;
Thromboangiitis Obliterans
4.Computed Tomography of Catamenial Hemoptysis.
In Han KIM ; Dong Seob JANG ; Tae Byung PARK ; Kwang Kon KOH ; Chul Ho CHO ; Chan Sup PARK ; Chang Hun LEE
Tuberculosis and Respiratory Diseases 1994;41(5):558-561
A 41-year-old female was admitted to our hospital for self-audible wheezing sound and dyspnea. On past history, she has been suffered from chest discomfort, and treated recurrently by other hospitals. But, there was no symptomatic improvement. A stridor and mixed wheezing sound was auscultated on whole lung field. PFT revealed fixed type or variable intra- & extra-thoracic air way obstructive pattern. By bronchoscopy & bronchogram, we found web-like structure on the distal trachea. A bronchoplasty was performed and the post-operative PFT showed slight improvement & she had no more complaints.
Adult
;
Bronchoscopy
;
Dyspnea
;
Female
;
Hemoptysis*
;
Humans
;
Lung
;
Respiratory Sounds
;
Thorax
;
Trachea
5.A mandibulotomy approach to malignant neoplasms of oral cavity and oropharynx.
Hong Chul KIM ; Sang Yoon KIM ; Bong Jae LEE ; Kwang Chol CHU ; Kyung Suck KOH ; Sang Hoon HAN
Korean Journal of Otolaryngology - Head and Neck Surgery 1993;36(1):117-122
No abstract available.
Mouth*
;
Oropharynx*
6.Gene Ploymorphisms of Angiotensin Converting Enzyme and Endothelial Nitric Oxide Synthase in Patients with IgA Nephropathy.
In Hee KIM ; Won KIM ; Sung Kyew KANG ; Dae Yul LEE ; Gou Young KOH ; Kwang Young LEE ; Sung Bae PARK ; Hyun Chul KIM ; Sung Kwang PARK
Korean Journal of Nephrology 1999;18(3):390-399
To evaluate the association between ACE gene I/D polymorphism and ecNOS gene a/b polymorphism in IgA nephropathy, 158 IgA nephropathy patients and 121 control subjects were examined. In genotype distribution of the ACE gene I/D polymorphism, there was no significant difference in genotype distribution between controls and IgA nephropathy patients. We also examined the association between ACE genotype and clinical characteristics in the patients with IgA nephropathy. The incidence of hypertension in patients with DD genotype was higher than that of other genotypes. There were no significant association between I/D polymorphism distribution and chronic renal failure, nephrotic range proteinuria, and glomerular sclerosis in IgA nephropathy. In genotype distribution of ecNOS gene a/b polymorphism, there was no significant difference between IgA nephropathy patients and controls. There was no significant difference in frequency of chronic renal failure, hypertension, nephrotic range proteinuria and glomerular sclerosis among ecNOS genotypes. In addition, we failed to detect any significant association between the ACE and ecNOS gene-polymorphis ms and the decline of renal function in IgA nephropathy. A further study with larger number of patient population would be necessary.
Angiotensins*
;
Genotype
;
Glomerulonephritis, IGA*
;
Humans
;
Hypertension
;
Immunoglobulin A*
;
Incidence
;
Kidney Failure, Chronic
;
Nitric Oxide Synthase Type III*
;
Peptidyl-Dipeptidase A*
;
Proteinuria
;
Sclerosis
7.Sonographic Analysis of Malignant Thyroid Nodules by Surgeon.
Gun GO ; Jin Chul KOH ; Sang Yong CHOI ; Shin Hee PARK ; Kwang Chan LEE ; Chin Seung KIM
Korean Journal of Endocrine Surgery 2010;10(4):224-228
PURPOSE: Ultrasound is most effective study for evaluating thyroid nodules. In this review, we discuss that sonographic findings to differentiate benign from malignant nodules and suggest recommendations for indications of fine needle aspiration biopsy and thyroid nodule management. METHODS: Sonographic scans of 206 thyroid nodules in 164 patients were candidated for this study. We evaluated sonographic findings by shape, calcification, margin, and echogenicity, retrospectively. Sonographic findings that suggested malignancy included microcalcifications, a speculated margin, marked hypoechogenicity and a shape that was taller than wide. The final diagnosis of lesion as benign (n=180) or malignant (n=26) was confirmed by fine needle aspiration biopsy and follow-up (>6 months). We demonstrated the difference of the sensitivity, specificity, positive predictive value, negative predictive value and accuracy. RESULTS: Of 206 thyroid nodules, 26 were malignant. The sensitivity, specificity, positive predictive value, negative predictive value and accuracy based on our sonographic classification method were 84.6%, 73.9%, 31.9%, 97.0% and 75.2%. CONCLUSION: Sonography can be helpful for making the differentiation between and malignant nodules. So, when well trained surgeon find thyroid nodules on sonography, we can make correct diagnosis of malignant nodules.
Biopsy
;
Biopsy, Fine-Needle
;
Classification
;
Diagnosis
;
Follow-Up Studies
;
Humans
;
Methods
;
Retrospective Studies
;
Sensitivity and Specificity
;
Thyroid Gland*
;
Thyroid Nodule*
;
Ultrasonography*
8.Rectus abdominis myocutaneous free flap for the reconstruction of oral cavity and oropharynx.
Kyung Bo SIM ; Kyung Suk KOH ; Sang Hoon HAN ; Kun Chul YOON ; Robert S CHUNG ; Sang Yoon KIM ; Kwang Chul CHOO
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(6):936-942
No abstract available.
Free Tissue Flaps*
;
Mouth*
;
Oropharynx*
;
Rectus Abdominis*
9.Various causes of dyspepsia: to determine organic and functional cause of dyspepsia.
Kwang Hyun RYU ; Young Ho KIM ; Hee Jung SON ; Poong Lyul RHEE ; Kwang Chul KOH ; Jae Jun KIM ; Seung Woon PAIK ; Jong Chul RHEE ; Kyoo Wan CHOI
Korean Journal of Gastrointestinal Motility 1998;4(2):112-117
BACKGROUND/AIMS: Dyspepsia is very common in the community. The aim of this study was to assess the frequency of various causes of dyspepsia. METHODS: Two hundreds nine patient with dyspepsia were investigated. Basic laboratory screening, ECG, Upper gastrointestinal endoscopy or upper gastrointestinal barium study, upper abdominal ultrasound were performed in every dyspeptic patients. RESULTS: Functional dyspepsia was the cause of symptoms in 92.3%, peptic ulcer in 2.9% (duodenal ulcer in five patients, gastric ulcer in one patient), reflux esophagitis in 0.5%, esophageal ulcer in 0.5%. Of dyspeptic patients, gallstone was found in 1.4%, gastric submucosal tumor in 1.0%, fatty liver in 1.9% (two of four patients with fatty liver had elevated transaminase), upper gastrointestinal cancer in 0%. Of functional dyspepsia patients, women was 60.3%, men was 39.7%. CONCLUSIONS: The most common cause of dyspepsia was functional dyspepsia. Various causes of organic dyspepsia was peptic ulcer, reflux esophagitis, and esophageal ulcer.
Barium
;
Dyspepsia*
;
Electrocardiography
;
Endoscopy, Gastrointestinal
;
Esophagitis, Peptic
;
Fatty Liver
;
Female
;
Gallstones
;
Gastrointestinal Neoplasms
;
Humans
;
Male
;
Mass Screening
;
Peptic Ulcer
;
Stomach Ulcer
;
Ulcer
;
Ultrasonography
10.A Case of Renal Transplantation in A Patient with Fabry's Disease.
Won KIM ; Hyeon Woo KOH ; Sung Kwang PARK ; Sung Kyew KANG ; Seung Ryel RHEE ; Hee Chul YU ; Baik Hwan CHO ; Min Chul KIM ; Kwang Young LEE
The Journal of the Korean Society for Transplantation 1998;12(1):111-116
Fabry's disease is a rare, inborn error, sex-linked disorder of glycosphingolipid metabolism with death occurring from myocardial or renal involvement at 4th or 5th decades. The primary metabolic defect lies in the deficient tissue activity of the enzyme alpha-galactosidase A which results in progressive accumulation of the specific neutral glycosphingolipids, cerebroside dihexoside(CDH) and cerebroside triihexoside(CTH), within the lysosomes of endothelial, perithelial and smooth muscle cells of the cardiovascular and renal systems predominantly. Clinical manifestations are sequelae of the anatomic and physiologic alterations produced by the progressive deposition of glycosphingolipid in the tissues. We report the first case of successful renal transplantation in a patient with Fabry's disease in Korea. The patient was a 33-year-old male. Fabry's disease was confirmed by measurement of serum alpha- galactosidase level and renal biopsy. Biopsy finding showed lamellar inclusion bodies on electron microscopy. Galactosidase activity was also markedly decreased. He has been well for 49 months.
Adult
;
alpha-Galactosidase
;
Biopsy
;
Fabry Disease*
;
Galactosidases
;
Humans
;
Inclusion Bodies
;
Kidney Transplantation*
;
Korea
;
Lysosomes
;
Male
;
Metabolism
;
Microscopy, Electron
;
Myocytes, Smooth Muscle
;
Neutral Glycosphingolipids
;
Transplantation