1.Clinicopathologic study of Castleman's disease in Korea.
Ji Eun KIM ; Chong Jai KIM ; In Ae PARK ; Woo Ho KIM ; Jeong Wook SEO ; Ja Jun JANG ; Chul Woo KIM ; Seong Hoe PARK ; Hyun Soon LEE ; Je G CHI ; Yong Il KIM ; Eui Keun HAM
Journal of Korean Medical Science 2000;15(4):393-398
Castleman's disease represents an atypical lymphoproliferative disorder, infrequently associated with various immunologic abnormalities or subsequent development of malignancy such as Kaposi sarcoma, malignant lymphoma and plasmacytoma. Its clinicopathologic features depend on various etiologic factors such as Kaposi sarcoma herpesvirus (KSHV), oversecretion of IL-6, adhesion molecule and follicular dendritic cell dysplasia, etc. To investigate the relationship of Castleman's disease (CD) and the above factors, we reviewed 22 cases of CD. Four cases of KSHV positive CD were detected, all multicentric, plasma cell type, and these cases displayed prominent vascular proliferation, characteristic 'Kaposi-like lesion'. IL-6 and CD54 positive mononuclear cells were scattered in interfollicular areas of KSHV positive cases. Follicular dendritic cell hyperplasia, vascular proliferation, expression of IL-6 and CD54 did not show any significant difference between solitary vs multicentric type, and plasma cell type vs hyaline vascular type. Our study suggests that KSHV positive CD reveals unique pathologic features, and the probable relationship of KSHV and IL-6 and CD54 is discussed.
Adolescence
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Adult
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Biological Markers
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Dendritic Cells, Follicular/pathology
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Epstein-Barr Virus Infections/virology
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Epstein-Barr Virus Infections/epidemiology
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Female
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Germinal Center/pathology
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Giant Lymph Node Hyperplasia/virology
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Giant Lymph Node Hyperplasia/pathology+ACo-
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Giant Lymph Node Hyperplasia/epidemiology
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Giant Lymph Node Hyperplasia/classification
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Herpesviridae Infections/virology
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Herpesviridae Infections/epidemiology
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Herpesvirus 4, Human/isolation +ACY- purification
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Herpesvirus, Kaposi Sarcoma-Associated/isolation +ACY- purification
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Human
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Hyperplasia
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Intercellular Adhesion Molecule-1/analysis
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Interleukin-6/analysis
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Korea/epidemiology
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Lymph Nodes/virology
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Lymph Nodes/pathology
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Lymph Nodes/chemistry
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Male
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Middle Age
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Neovascularization, Pathologic
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Receptors, Complement 3d/analysis
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Retrospective Studies
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Tumor Virus Infections/virology
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Tumor Virus Infections/epidemiology
2.A comparison study on allergen components between Korean (Arachis fastigiata Shinpung) and American peanut (Arachis hypogaea Runner).
Chun Wook PARK ; Gyeong Il KIM ; Cheol Heon LEE
Journal of Korean Medical Science 2000;15(4):387-392
The prevalence of peanut allergy in Korea is lower than in America. Peanut extract allergens between the two countries have not been standardized. This study was performed to compare the allergenicity of raw Korean and American peanuts with that of roasted peanuts. We prepared the peanut extracts in Korean raw (KP) and roasted peanuts (KRP), and also in American raw (AP) and roasted (ARP) peanuts. We compared the peanut extract allergens of KP, KRP, AP and ARP in vitro with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) followed by immunoblotting, T-cell proliferation assay and skin prick test with sera from peanut-allergic patients. SDS-PAGE and Western blotting demonstrated four allergenic extracts, numerous bands that displayed a high prevalence of IgE binding. IgE-binding bands were at 64, 36 and 17 kDa. Western blot inhibition revealed that either KP or AP could almost completely inhibit the reactivity of the other extract. There were no differences between T-cell proliferation assay and skin prick test. In conclusion, this investigation showed no different allergic components in both raw and roast extracts of Korean and American peanuts.
Allergens/immunology
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Allergens/analysis+ACo-
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Allergens/adverse effects
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Blotting, Western
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Cells, Cultured
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Comparative Study
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Electrophoresis, Polyacrylamide Gel
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Food Hypersensitivity/immunology
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Heat
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Human
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Hybridization
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Korea
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Lymphocyte Transformation
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North America
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Peanuts/immunology
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Peanuts/classification
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Peanuts/chemistry+ACo-
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Plant Extracts/immunology
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Plant Proteins/immunology
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Plant Proteins/analysis+ACo-
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Plant Proteins/adverse effects
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Skin Tests
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Species Specificity
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T-Lymphocytes/immunology
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T-Lymphocytes/drug effects
3.Influence of menopause on high density lipoprotein-cholesterol and lipids.
Chee Jeong KIM ; Tae Ho KIM ; Wang Seong RYU ; Un Ho RYOO
Journal of Korean Medical Science 2000;15(4):380-386
It has been generally accepted that high density lipoprotein cholesterol (HDL-C) level decreases with menopause in women. However, recent reports show different results. There is very little data concerning perimenopausal women. To verify these findings, lipids and lipoprotein(a) +AFs-Lp(a)+AF0- levels were compared among pre-, peri- and postmenopausal women of similar mean ages. Postmenopausal women had higher HDL-C levels than premenopausal women (p+ADw-0.001) and there was no difference between peri- and postmenopausal women. LDL-C level in perimenopausal women was lower than in postmenopausal women (p+ADw-0.001) and higher than in premenopausal women with borderline significance (p+AD0-.051). Total cholesterol levels showed stepwise elevation from premenopause to postmenopause. Perimenopausal women had lower Lp(a) levels than postmenopausal women (p+ADw-0.0005) and similar levels to premenopausal women. Lp(a) levels between 0.1 to 10.0 mg/dL were the most prevalent in pre- and perimenopausal women, and those between 10.1 to 20.0 mg/dL in postmenopausal women. In conclusion, menopause itself is associated with the elevation of HDL-C level, and the postmenopausal increase of coronary artery disease is not related to postmenopausal change of HDL-C level. Perimenopausal status, although transient, may favor Lp(a) and lipid profiles for delaying atherosclerosis.
Apolipoproteins A/blood
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Arteriosclerosis/epidemiology
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Biological Markers
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Cholesterol/blood
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Comparative Study
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Cross-Sectional Studies
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FSH/blood
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Female
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Human
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Lipids/blood+ACo-
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Lipoprotein(a)/blood
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Lipoproteins, HDL Cholesterol/blood+ACo-
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Menopause/blood+ACo-
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Middle Age
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Postmenopause/blood
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Premenopause/blood
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Risk Factors
4.Ultrasound examination of gastrointestinal tract diseases.
Journal of Korean Medical Science 2000;15(4):371-379
With recent technical advances, increasing use of sonography in the initial evaluation of patients with abdominal disease may allow the detection of unexpected tumor within the abdominal cavity. Easiness of sonographic detection of bowel pathology, purposely or unexpectedly, warrants the inclusion of bowel loops during ultrasound examination when a patient complains of symptoms indicating diseases of the bowel. In patients complaining of acute abdominal symptoms or nonspecific gastrointestinal symptoms and showing signs such as abdominal pain, diarrhea, hematochezia, change of bowel habit, or bowel obstruction, sonography may reveal the primary causes and may play a definitive role in making a diagnosis. On ultrasonography, abnormal lesions may appear as fungating mass with eccentrically located bowel lumen (pseudokidney sign) or symmetrical or asymmetrical, encircling thickening of the colonic wall (target sign). In patients with mass or wall thickening detected on ultrasonography, additional work-up such as barium study, CT or endoscopy would be occasionally necessary for making a specific diagnosis.
Abdomen, Acute/ultrasonography
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Aged
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Appendicitis/ultrasonography
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Colorectal Neoplasms/ultrasonography
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Diverticulitis/ultrasonography
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Female
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Gastrointestinal Diseases/ultrasonography+ACo-
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Gastrointestinal Neoplasms/ultrasonography
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Human
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Inflammatory Bowel Diseases/ultrasonography
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Intestinal Obstruction/ultrasonography
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Intestinal Perforation/ultrasonography
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Intestines/ultrasonography
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Male
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Stomach/ultrasonography
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Ultrasonography/instrumentation
5.Cystic fibrosis: a case presented with recurrent bronchiolitis in infancy in a Korean male infant.
Hyung Ro MOON ; Tae Sung KO ; Young Youl KO ; Jung Hwan CHOI ; Young Chi KIM
Journal of Korean Medical Science 1988;3(4):157-162
The aim of this case report is to draw the attention to the occurrence of cystic fibrosis (C.F.) in a Korean infant and thus increase the awareness for the diagnosis. The male infant was presented with a history of recurrent bronchiolitis manifested by severe cough, wheeze and dyspnea from three weeks of age, in whom the diagnosis of C.F. was clinically suspected and was confirmed by demonstration of two elevated sweat chloride levels (97 mEq/L and 99 mEq/L) in the patient. The diagnosis was delayed because the main manifestations of C.F. were the same as the main symptoms of common diseases such as cough, diarrhea and failure to thrive. C.F. is probably underdiagnosed in Korean population both because the diagnosis is not considered since the disease is thought to be uncommon or even not to occur and because diagnostic facilities including the quantitative iontophoresis sweat test are lacking.
Bronchiolitis/diagnosis/*etiology
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Cystic Fibrosis/complications/*diagnosis/ethnology
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Humans
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Infant
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Male
6.Hepatic amyloidosis: two cases report.
Hyeon Joo JEONG ; Eun Kyung HAHN ; Eung KIM ; Chan Il PARK
Journal of Korean Medical Science 1988;3(4):151-155
Amyloidosis is classified according to the distribution pattern of amyloid deposition sites and associated diseases. Hepatic amyloidosis is not infrequent, although rarely causes clinical liver disease. We report two cases of amyloidosis diagnosed by liver biopsy. One presented with symptoms related almost to the liver disease, such as jaundice, hepatomegaly and indigestion. Echocardiogram revealed hypertrophic cardiomyopathy, suggesting cardiac involvement of the amyloidosis. The patient died of hepatic failure. The other case was found in a patient with an end stage renal disease. Features of congestive heart failure in this case may reflect cardiac involvement. The pattern of hepatic amyloid deposition in both of these cases was diffuse perisinusoidal. The predominant intralobular deposition suggests that these are amyloidosis of the secondary type.
Amyloidosis/*diagnosis/pathology
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Humans
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Liver Diseases/*diagnosis/pathology
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Male
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Middle Aged
7.Refractoriness to platelet transfusion after single-donor consecutive platelet transfusions and its relationship to platelet antibodies.
Munho LEE ; Byoung Kook KIM ; Seonyang PARK ; Cheolwon SUH ; Myoung Hee PARK ; Myong Joon CHO
Journal of Korean Medical Science 1988;3(4):143-149
In thirty patients with acute leukemia and severe aplastic anemia receiving random single donor platelet transfusions, the development of refractoriness by consecutive platelet transfusions with cytapheresis and its relationship to the appearance of anti-platelet antibodies were investigated. The median number of platelet transfusions inducing refractoriness was 13 times, and 20% of the patients remained unrefractory despite of the repeated multiple platelet transfusions up to 20 to 25 times. The results of anti-platelet antibody tasts by the enzyme-linked immunosorbent assay(ELISA) and immunofluorescent techniques(IFT) showed no statistically significant relationship with the refractoriness (p greater than 0.1). Although there was significant correlation between the results of ELISA and IFT, both tests were insufficient to find out refractoriness even with the use of pooled platelets from multiple donors as target cells. This study shows that 13 single donor platelet transfusions result in refractoriness, that both ELISA and IFT are insufficient to detect refractoriness despite of their significant correlation, and that other methods than these are needed in order to detect alloimmunization.
Adolescent
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Adult
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Aged
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Anemia, Aplastic/therapy
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Anemia, Refractory/*etiology
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Antibodies/metabolism
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*Blood Platelets/immunology
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*Blood Transfusion
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Female
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Humans
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Leukemia/therapy
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Male
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Middle Aged
8.Multicenter report on dialysis and transplantation in Korea, 1986: Korean Society of Nephrology.
Journal of Korean Medical Science 1988;3(4):135-141
Since 1981, the Korean Society of Nephrology began annual report on renal replacement therapy in Korea. The annual number of new patients receiving dialysis treatment in 1986 increased to 957 patients (23.3 per million population) from 825 patients (20.4 per million population) in 1985. And the total number of patients on replacement therapy increased from 1,508 patients (37.3 per million population) to 2,534 patients (61.7 per million population). 1,340 patients (32.6 per million population) of these patients were on hemodialysis, 573 patients (13.9 per million population) on continuous ambulatory peritoneal dialysis (CAPD) and 621 patients (15.1 per million population) on functioning renal graft as of December 31, 1986. The common causes of renal failure of new patients were chronic glomerulonephritis (41.6%) followed by diabetic nephropathy (12.6%), nypertensive nephrosclerosis (7.8%), chronic pyelonephritis (2.5%) and others. The annual mortality rate decreased from 21.9% in 1981 to 13.5 in 1986. The common causes of death in patients on dialysis therapy were cardiac (32.8%), vascular (14.7%), infective (14.7%) and social problems (11.2%) in the order of frequency. Recently, the number of patients requiring dialysis is rapidly increasing due to expanded medical insurance support for dialysis and improved economic status of our country. Therefore, it is necessary to draw up counterplan for a rapid growth of the number of new patients.
Hepatitis B/etiology
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Humans
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Kidney Failure, Chronic/epidemiology/*therapy
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*Kidney Transplantation
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*Kidneys, Artificial/adverse effects
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Korea
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Multicenter Studies as Topic
9.Gliosarcoma: a case with unusual epithelial feature.
Dong Sug KIM ; Shin Kwang KANG ; Je Geun CHI
Journal of Korean Medical Science 1999;14(3):345-350
Astrocytic tumors, particularly gliosarcoma, may contain epithelial features in the form of trabecular, adenoid, papillary arrangement, and squamous metaplasia. A case of gliosarcoma with unusual epithelial feature is described. The patient was a 60-year-old male with frequent seizures. The mass was 4 cm and in the left frontal lobe. Trabecular or rarely adenoid arrangement of neoplastic astrocytes was present in the mucinous stroma, and there was a distinctive transition between the trabecular area and typical anaplastic astrocytoma. The tumor cells in the trabecular area showed positive immunostain for glial fibrillary acidic protein, but did not react with various kinds of cytokeratin. The sarcomatous area was undifferentiated and was not labeled by factor-VIII, desmin, and anti-smooth muscle actin. Occurrence and histogenesis of epithelial features in gliosarcoma are reviewed. The importance to recognize the existence of epithelial feature in malignant astrocytic tumor is emphasized.
Brain Neoplasms/surgery
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Brain Neoplasms/pathology*
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Case Report
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Epithelium/pathology
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Gliosarcoma/surgery
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Gliosarcoma/pathology*
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Human
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Magnetic Resonance Imaging
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Male
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Middle Age
10.Non-typhoid Salmonella meningitis complicated by a infarction of basal ganglia.
Hyunmi KIM ; Jin Yeoung JEOUNG ; Soo Youn HAM ; Sung Ryul KIM
Journal of Korean Medical Science 1999;14(3):342-344
A previously healthy 16-month-old Korean girl with symptoms of fever, vomiting, and generalized tonic seizure was diagnosed to have Group D non-typhoid Salmonella meningitis. The patient was treated with ceftriaxone (100 mg/kg/day) and amikin (22.5 mg/kg/day) initially and ciprofloxacin (30 mg/kg/day) was added later because of clinical deterioration and disseminated intravascular coagulation. Brain CT performed on the second day showed a well-demarcated low density lesion in the right lentiform nucleus and both caudate nuclei, without evidence of increased intracranial pressure. MRI performed on the 11th day confirmed CT scan findings as well as right subdural fluid collection, brain atrophy, and ventriculomegaly. She underwent subdural drainage and later ventriculo-peritoneal shunt operation. Despite receiving intensive treatment, she still has severe neurologic sequelae. Our case shows that infarctions of basal ganglia and thalami are not specific for tuberculous meningitis and that meningitis complicated by infarction is indicative of grave prognosis.
Basal Ganglia Diseases/radiography
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Basal Ganglia Diseases/pathology
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Basal Ganglia Diseases/complications
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Basal Ganglia Diseases/cerebrospinal fluid
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Brain/radiography
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Brain/pathology
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Case Report
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Cerebral Infarction/radiography
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Cerebral Infarction/pathology
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Cerebral Infarction/complications*
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Cerebral Infarction/cerebrospinal fluid
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Female
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Follow-Up Studies
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Human
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Infant
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Magnetic Resonance Imaging
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Meningitis, Bacterial/radiography
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Meningitis, Bacterial/pathology
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Meningitis, Bacterial/complications*
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Meningitis, Bacterial/cerebrospinal fluid
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Salmonella Infections/complications*
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Tomography, X-Ray Computed/methods