1.A case of infrahyoid ectopic thyroid gland.
Ki Hwan HONG ; Mi Jung KIM ; Sang Sul JUNG
Korean Journal of Otolaryngology - Head and Neck Surgery 1993;36(6):1363-1366
No abstract available.
Thyroid Dysgenesis*
2.Laryngeal adjustments for the Korean stops affricates and fricatives: electromyographic studies.
Ki Hwan HONG ; Dong Suk CHON ; Mi Jung KIM ; Kil Yang JUNG ; Young Ki KIM
Korean Journal of Otolaryngology - Head and Neck Surgery 1991;34(5):1008-1017
No abstract available.
3.A clinical evaluation of nodular thyroid disease.
Ki Hwan HONG ; Mi Jung KIM ; Kil Yang JUNG ; Sam Hyun KWON
Korean Journal of Otolaryngology - Head and Neck Surgery 1992;35(5):664-669
No abstract available.
Thyroid Diseases*
;
Thyroid Gland*
4.A Case of Eosinophilic Myocarditis associated with Hypereosinophilia showing Myocardial Edema.
Mi Seung SHIN ; Yung Mi ANN ; Hong Keun CHO ; Gil Ja SHIN ; Nam Shik JUNG ; Sang Ho CHO
Korean Circulation Journal 1998;28(2):296-303
Chusid et al proposed diagnostic criteria of hypereosinophilic syndrome (HES) that remain valid today. These were, (1) a sustained peripheral blood eosinophil count of more than 1500/L present for longer than 6 months ; (2) no evidence of other apparent causes for eosinophilia, and (3) presumptive signs of parenchymal organ involvement. Any organ system may be affected in HES, but the most severe clinicopathological involvements are of the heart and nervous system. Although multiple organ systems may be involved, the most common cause of morbidity and mortality is cardiac involvement with extensive fibrous thickening of the endomyocardium and overlying thrombus. We report a case of acute peri-myocarditis with eosinophilia, which was confirmed as eosinophilic myocarditis by endomyocardial biopsy, with literature review.
Biopsy
;
Edema*
;
Eosinophilia
;
Eosinophils*
;
Heart
;
Hypereosinophilic Syndrome
;
Mortality
;
Myocarditis*
;
Nervous System
;
Thrombosis
5.A Case of Eosinophilic Myocarditis associated with Hypereosinophilia showing Myocardial Edema.
Mi Seung SHIN ; Yung Mi ANN ; Hong Keun CHO ; Gil Ja SHIN ; Nam Shik JUNG ; Sang Ho CHO
Korean Circulation Journal 1998;28(2):296-303
Chusid et al proposed diagnostic criteria of hypereosinophilic syndrome (HES) that remain valid today. These were, (1) a sustained peripheral blood eosinophil count of more than 1500/L present for longer than 6 months ; (2) no evidence of other apparent causes for eosinophilia, and (3) presumptive signs of parenchymal organ involvement. Any organ system may be affected in HES, but the most severe clinicopathological involvements are of the heart and nervous system. Although multiple organ systems may be involved, the most common cause of morbidity and mortality is cardiac involvement with extensive fibrous thickening of the endomyocardium and overlying thrombus. We report a case of acute peri-myocarditis with eosinophilia, which was confirmed as eosinophilic myocarditis by endomyocardial biopsy, with literature review.
Biopsy
;
Edema*
;
Eosinophilia
;
Eosinophils*
;
Heart
;
Hypereosinophilic Syndrome
;
Mortality
;
Myocarditis*
;
Nervous System
;
Thrombosis
6.Intraductal Variant of Peripheral Cholangiocarcinoma of the Liver A report of three cases.
Won Mi LEE ; Seok Hoon JEON ; Eun Kyung HONG ; Moon Hyang PARK ; Jung Dal LEE
Korean Journal of Pathology 1998;32(3):222-225
Intraductal variant of peripheral cholangiocarcinoma is extremely rare. This variant shows intraductal growth and intraluminal extension without any infiltrative growth. The mode of intraductal growth is not known. The prognosis of this variant is better than that of usual cholangiocarcinoma. We report three cases, one of which is associated with Clonorchis sinensis (CS) infection. The tumors were entirely confined within the dilated peripheral tributaries of the intrahepatic bile duct. Microscopically, the tumors were well to moderately well differentiated, with a papillary or a micropapillary growth pattern. Focal clear cytoplasmic change and mucin production were noted. The tumors showed intraductal spreading without any invasion to the liver parenchyme. Mucosal hyperplasia and dysplasia were noted in the adjacent ducts. The authors assume that intraductal cholangiocarcinoma is a distinct subtype, and persistent irritation, such as, CS infection may undergo a malignant transformation through mucosal dysplasia.
Bile Ducts, Intrahepatic
;
Cholangiocarcinoma*
;
Clonorchis sinensis
;
Cytoplasm
;
Hyperplasia
;
Liver*
;
Mucins
;
Prognosis
7.Immunohistochemical Study of the Multidrug Resistant(MDR) Gene Expression in Gastric Carcinoma.
Jung Hee HAN ; Byung Gon PARK ; Mi Sook ROH ; Sook Hee HONG
Korean Journal of Pathology 1994;28(1):38-48
We performed immunohistochemical stain of p-glycoprotein using JSB-1 monoclonal antibody to study multidrug resistant(MDR) gene expression in 137 gastric tumor tissues obtained from 87gastric carcinoma patients. The incidence of p-glycoprotein expression was 60 of 87 cases(69%) and it was not correlated with age, sex, depth of tumor invasion, and lymph node metastasis, but was correlated with histologic type of gastric adenocarcinoma. The distribution of p-glycoprotein positive cells in the tumor tissue was diffuse in 34 cases(73.9%) and focal in 12 cases(26.1%), and the dominant staining patterns of p-glycoprotein in the tumor cells were cytoplasmic and golgi staining in 20 cases(43.5%) and 19 cases(41.3%), respectively, and 7 cases(15.2%) showed fine granules in the cytoplasm. The incidence of p-glyco-protein expression in the tumor tissue was higher in A and AB blood type patients who have A antigen than in 0 and B blood type patients. Cytoplasmic staining pattern was dominant in O and B blood types and golgi staining in A and AB blood type patients. Among 27 patients 'who received chemotherapy, partial remission was noted in 9 of 11 p-glyco-protein negative patients(81.8%) and no remission or progression of the tumor was seen in 9 of 16 p-glycoprotein positive patient(56.3%). The p-glycoprotein expression in gastric carcinoma had no direct correlation with known several prognostic factors of the gastric tumor except for histologic type, and it is supposed that p-glycoprotein detection in gastric tumor tissue by immunohisto-chemical stain is a good method for predicting the response of chemotherapy, especially in p-gly-coprotein negative cases.
Incidence
8.A Clinical Observation of Neonatal Hyperbilirubinemia due to ABO Incompatibility.
Mi Jung KOH ; Young Kyun LEE ; Jin Hong PARK ; Yeon Kyun OH
Journal of the Korean Pediatric Society 1990;33(9):1194-1201
No abstract available.
Hyperbilirubinemia, Neonatal*
9.Correlation between Body Fat Percent Estimated by Bioelectrical Impedance Analysis and Other Variable Methods .
Hye Won YOM ; Su Jung KIM ; Il Tae WHANG ; Young Mi HONG
Journal of the Korean Pediatric Society 2003;46(8):751-757
PURPOSE: Obesity is a significant health problem with medical and psychological consequences for children and adolescents. The purpose of this study was to assess the correlation between body fat percent using bioelectrical impedance(BI) and other variable methods. METHODS: We measured height, weight, body mass index(BMI) and body fat percent by skinfold thickness(ST) and BI in 1,035(496 male; 539 female) children from seven to 18 years of age. The correlation coefficients between BI and each of the other different methods were obtained. The sensitivity and specificity to predict obesity by these several methods were studied. RESULTS: Fat percent estimated by BI analysis and BMI showed a strong correlation(r=0.749). Fat percent estimated by BI analysis and ST showed a very strong correlation(r=0.835). At the 95th percentile cut-off point for BI, ST showed a sensitivity of 57.7%, and a specificity of 97.6% for estimating body fat. At the 95th percentile cut-off point for BI, BMI showed a sensitivity of 84.9%, and a specificity of 99.3% for estimating body fat. CONCLUSION: The fat percent estimated by BI analysis correlated strongly with ST or BMI. BI analysis is an objective and accurate method for estimating body fat in childhood obesity.
Adipose Tissue*
;
Adolescent
;
Body Mass Index
;
Body Weight
;
Child
;
Electric Impedance*
;
Humans
;
Male
;
Obesity
;
Pediatric Obesity
;
Sensitivity and Specificity
;
Skinfold Thickness
10.Immunohistochemical Findings in 10 Cases of Inflammatory Myofibroblastic Tumor.
Soo Jin JUNG ; Mi Seon KANG ; Chang Hoon LEE ; Sook Hee HONG ; Hye Kyoung YOON
Korean Journal of Pathology 1999;33(9):717-722
A wide range of denomination has been used for inflammatory myofibroblastic tumor (IMT). IMT is not entirely homogeneous, even though it shows some overlapping histologic features such as haphazard proliferation of spindle cell and polymorphic chronic inflammatory cell infiltraion. The spindle cell is considered to be of myofibroblastic origin but follicular dendritic cell origin was reported recently. IMT is known as nonneoplastic, aberrant inflammatory response. However, IMT could show local invasion, recurrence, vascular invasion, and malignant transformation, and clonal characteristics and aneuploidy of IMT support the hypothesis that IMT may be a neoplastic process. In order to define the nature of spindle cell of IMT, immunohistochemical stains for smooth muscle actin (SMA), vimentin (VMT), lysozyme, S-100 protein, cytokeratin, CD21 were done. Additional immunohistochemical stains for MIB-1 for proliferating activity and LMP (latent membrane protein) for Epstein-Barr virus (EBV) were done. IMTs were composed of each 2 cases from lung, liver and lymph node and one case from common bile duct, maxillary sinus, bladder and thigh, and were histologically subclassified according to Coffin et al. Nine cases (90%) were positive for SMA and VMT, but no correlation between SMA and VMT immunoreactivity and histologic types was identified. Five cases (50%) were positive for lysozyme and S-100 protein, and histologic type III was negative for lysozyme and S-100 protein, and immunoreactivity for S-100 protein was different according to the histologic subtypes. All 11 cases were negative for CD21 and EBV LMP. MIB-1 labelling index was less than 1% in all cases. In summary, the spindle cell is regarded as myofibroblastic origin rather than follicular dendritic cell origin. Relationship with EBV is not clear, and negligible MIB-1 reaction suggests that IMT might have a good prognosis.
Actins
;
Aneuploidy
;
Coloring Agents
;
Common Bile Duct
;
Dendritic Cells, Follicular
;
Herpesvirus 4, Human
;
Immunohistochemistry
;
Keratins
;
Liver
;
Lung
;
Lymph Nodes
;
Maxillary Sinus
;
Membranes
;
Muramidase
;
Muscle, Smooth
;
Myofibroblasts*
;
Prognosis
;
Recurrence
;
S100 Proteins
;
Thigh
;
Urinary Bladder
;
Vimentin