1.Congenital Cystic Adenomatoid Malformation of the Lung: Clinicopathologic analysis of 22 cases.
Young Lyun OH ; Yeon Lim SUH ; Je G CHI
Korean Journal of Pathology 1994;28(3):219-227
Congenital cystic adenomatoid malformation of the lung(CCAML) is a rare developmental anomaly characterized by an "adenomatoid" hyperplasia of terminal respiratory structures with formation of the cysts of varying sizes. CCAML is separated into three major types based on the gross and microscopic findings. We have analyzed 22 cases of CCAML, those consisted of 6 autopsy cases and 16 surgical specimens. Out of 22 cases, 5 cases were composed of large cysts(type I) and 9 cases had multiple small cysts(type II). Remaining one case revealed features of solid type(type III), and 7 cases were mixed form. There were 16 boys and 6 girls. All cases were below the age of 14 years. There was no clear-cut age difference between different types of CCAML. However, inflammation, fibrosis and pseudostratification of epithelium were often found in older age. All fetal autopsy cases of CCAML had hydrops fetalis and were associated with maternal hydramnios. One case of type III showed definite mucinogenic cells in the cysts unexpectedly, and one case of the mixed form(typeI+II+III) was found in a fetus of 22 weeks of gestational age. Above findings contradicted the classical description of the CCAML, and suggested that arbitrary classification into three types may not be the best way in understanding this condition.
Cysts
2.Fibrocalcific Nodule in the Liver Capsule Caused by Ascaris Eggs: A case report.
Yeon Lim SUH ; So Young PARK ; Je G CHI
Korean Journal of Pathology 1992;26(4):411-413
Ascariasis is probably the most common helminthic infestation of man, but it seldom causes severe illness. Pathologic conditions of Ascaris may be caused by adult worms, eggs or larvae. We describe a case of Ascaris egg granulomas that were found incidentally on the surface of the liver in a 75-year-old woman who had undergone a segmentectomy for an intrahepatic stone. Grossly, there were several yellowish calcific nodules of 0.4 cm in diameter on the lateral surface of the left lobe of the liver. Microscopically, the lesions were located in the hepatic capsule and consisted of fibrocalific nodules with many eggs. The eggs were round to oval, thick-shelled and measured 50~75x30~50 um. Most of the morphologically preserved eggs were fertilized eggs, but they had smooth shells without external protein coats. This case is of interest for the unusual location of the lesion, the presence of eggs without mammillation, and the association with the intrahepatic stone.
Adult
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Male
;
Female
;
Humans
3.Cerebral Amyloid Angiopathy: A report of two cases.
Kee Taek JANG ; Ghee Young CHOE ; Yeon Lim SUH ; Je Geun CHI
Korean Journal of Pathology 1999;33(9):741-744
Cerebral amyloid angiopathy (C.A.A) is characterized by the extracellular amyloid protein deposition in the vessel walls of the brain and meninges. It has been estimated to account for 5 to 10% of all primary, nontraumatic brain hemorrhage. We report two cases of C.A.A causing nontraumatic intracerebral hemorrhage in the frontal lobe. The first case was a 60-year-old female who was admitted for the left hemiplegia and dysarthralgia. Brain CT revealed right frontal lobe hemorrhage. The second case was a 72-year-old male who was admitted for amnesia and gait disturbance. Clinical impression was Alzheimer's disease. Brain MRI revealed multifocal small hemorrhage in the right frontal lobe. Microscopically, both cases showed dilated small arteries of superficial cortex and meninges with hyalinization. Some vessels showed microaneurysm and fibriniod necrosis. Congo-red stain also exhibited birefringence under polarized light. There was no evidence of Alzheimer's disease.
Aged
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Alzheimer Disease
;
Amnesia
;
Amyloid
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Arteries
;
Birefringence
;
Brain
;
Cerebral Amyloid Angiopathy*
;
Cerebral Hemorrhage
;
Female
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Frontal Lobe
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Gait
;
Hemiplegia
;
Hemorrhage
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Humans
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Hyalin
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Intracranial Hemorrhages
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Magnetic Resonance Imaging
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Male
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Meninges
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Middle Aged
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Necrosis
4.Mortality Rates and Risk Factors in Community Based Dementia Patients.
Sookyung PARK ; Jun Young LEE ; Guk Hee SUH ; Sung Man CHANG ; Maeng Je CHO
Journal of Korean Geriatric Psychiatry 2007;11(1):25-28
OBJECTIVES: The aim of this study was to investigate mortality rates and risk factors in dementia patients in a rural cohort. METHODS: A total of 114 subjects with clinically diagnosed dementia were followed up for eight years from 1997 to 2005. Their mortality was compared with sociodemographic and clinical variables using the Cox proportional hazards models after adjusting age, sex, and education. RESULTS: During follow-up, the mortality rate of subjects was 80.2% and the mean (SD) duration of survival from at diagnosis to death was 4 years. Mortality in subjects with dementia depended on old age (relative risk [RR] : 1.05 ; 95% confidence interval [CI] : 1.01-1.08), male (RR : 1.61 ; CI : 1.00-2.59), low Clinical Dementia Rating scale (RR : 1.54 ; CI : 1.14-2.10), low Activities of Daily Living (RR : 0.72 ; CI : 0.59-0.89), low Instrumental Activities of Daily Living (RR : 0.83 ; CI : 0.75-0.92), no physical activity (RR : 0.44 ; CI : 0.28-0.70), smoking (RR : 1.74 ; CI : 1.05-2.89). CONCLUSION: Mortality in dementia depended on age, sex, CDR, ADL, IADL, physical activity, smoking. These findings have important implications that contribute to make the disease management of dementia patients.
Activities of Daily Living
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Cohort Studies
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Dementia*
;
Diagnosis
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Disease Management
;
Education
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Follow-Up Studies
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Humans
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Male
;
Mortality*
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Motor Activity
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Proportional Hazards Models
;
Risk Factors*
;
Smoke
;
Smoking
5.A Family of Facioscapulohumeral Muscular Dystrophy.
Young Hwan CHOI ; Youn Keun HWANG ; Young Ik SEO ; Moon Soo KANG ; Hang Jae KIM ; Nung Soo KIM ; Chung Kyu SUH ; Je Geun CHI
Journal of the Korean Neurological Association 1993;11(1):121-126
Facioscapulohumeral muscular dystrophy (FSHD) is a genetically trarlsmitted benign muscular dystrophy which has autosomal dominant inheritance pattern. It starts anytime within the first 30 years of life, and usually involves the face and shoulder girdle, and finally the pelvic muscles with very slow progression. Authors-report a fanily consisting of a father, two sons and one daughter, who had suffered from exertional dyspnea, weakness of facial muscle and winged scapulae, all wlth a slow progressive course. Two of these patients were biopsied arld confirmed light microscopically and electron microsopically.
Dyspnea
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Facial Muscles
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Fathers
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Humans
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Inheritance Patterns
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Muscles
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Muscular Dystrophies
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Muscular Dystrophy, Facioscapulohumeral*
;
Nuclear Family
;
Scapula
;
Shoulder
6.Development of De Novo Cavernous Hemangioma after Radiosurgery for Cavernous Hemangioma.
Je Young YEON ; Yeon Lim SUH ; Jong Hyun KIM ; Jung Il LEE
Journal of Korean Neurosurgical Society 2010;48(6):532-533
We report a rare case of cavernous hemangioma (CH) which developed in adjacent location to a preexisting CH after gamma knife radiosurgery (GKRS). A 36-year-old woman underwent GKRS for a CH in the left lentiform nucleus. Three-and-half years after radiosurgery, MRI revealed a new CH in the left caudate nucleus. Surgical excision of the new lesion was performed. The pathological examination confirmed the diagnosis of CH. In radiosurgery for CH, it should be noted that a new CH may develop, which is likely to result from the interaction between radiation and predisposing factors of the patient.
Adult
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Caudate Nucleus
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Caves
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Corpus Striatum
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Female
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Hemangioma, Cavernous
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Humans
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Radiosurgery
7.The effects on serum lipoprotein(a) of antihyperlipidemic agents.
Ki Tae KIM ; Sung Je PARK ; Young Sung SUH ; Dae Hyun KIM ; Dong Hak SHIN
Journal of the Korean Academy of Family Medicine 2000;21(2):234-243
BACKGROUND: Many studies to reduce serum lipoprotein(a) are done because serum lipoprotein(a) has been known to be an independent risk factor of coronary artery disease along with age, smoking, diabetes, hypertension, and hyperlipidemia. Till now, oral estrogen/androgen therapy, niacin analogue and plasmapheresis are known therapeutic methods. This study examined the relative effects of three antihyperlipidemic agents, acipimox, lovastatin, fenofibrate. METHODS: Among 70 subjects (male-19, female-51) with their serum cholesterol level of more than 240mg/dL, 56 subjects who were completed 2 months antihyperlipidemic treatment (acipimox-20, lovastatin-18, fenofibrate-18) were examined for baseline total cholesterol, HDL cholesterol, triglyceride, and lipoprotein(a) and were followed up 2 months later. RESULTS: Mean values of each group for acipimox, lovastatin, fenofibrate were as follows: total cholesterol (268.1+/-19.03, 287.1+/-36.42, 268.9+/-25.99), HDL cholesterol (43.5+/-10.99, 42.7+/-11.88, 37.9+/-8.20), triglyceride (226.1+/-165.03, 260.4+/-175.98, 234.3+/-124.33), LDL cholesterol (179.3+/-30.40, 192.3+/-41.52, 184.1+/-38.08), lipoprotein(a) (26.2+/-15.32,34.8+/-18.56,29.9+/-12.58). Mean percentile reduction of lipoprotein(a) was acipimox-41.4%(P<0.0001), lovastatin-22.2%(P<0.0001), fenofibrate-16.1%(P<0.05), and p value was less than 0.05 in the comparison of groups. Lipoprotein(a) showed no relations with age, sex, BMI, WHR, smoking, total cholesterol, HDL cholesterol, triglyceride and LDL cholesterol. After 2 months treatment, mean reduction percentages of total cholesterol was acipimox-12.2%(P<0.0001), lovastatin-17.6%(P<0.0001), fenofibrate-8.85%(P<0.05). LDL cholesterol was acipimox-16.12%(P<0.0001), lovastatin-22.89%(P<0.0001), fenofibrate-12.06% (P<0.05). Triglyceride was acipimox-17.24%(P<0.0001), lovastatin-17.39%(P<0.0001), fenofibrate-9,78%(P<0.05). HDL cholesterol was elevated in acipimox-17.24%(P<0.05), lovastatin-16.10%(P<0.05) and fenofibrate-12.06(P<0.05). In total cholesterol(P<0.05) and LDL cholesterol(P<0.05), there were significant differences among 3 groups, but not in HDLcholesterol and triglycerides. CONCLUSION: In two months treatment of acipimox, lovastatin and fenofibrate in hyperlipidemic patients, lipoprotein(a), known for independent risk factor of coronary artery disease, was reduced significantly in the order of acipimox, lovastatin and fenofibrate.
Cholesterol
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Cholesterol, HDL
;
Cholesterol, LDL
;
Coronary Artery Disease
;
Fenofibrate
;
Humans
;
Hyperlipidemias
;
Hypertension
;
Lipoprotein(a)*
;
Lovastatin
;
Niacin
;
Plasmapheresis
;
Risk Factors
;
Smoke
;
Smoking
;
Triglycerides
8.Histomorphometric evaluation of bone healing with natural calcium carbonatederived bone substitutes in rat calvarial defect.
Chung Ho LEE ; Je Hee JANG ; Jae Mok LEE ; Jo Young SUH ; Jin Woo PARK
The Journal of the Korean Academy of Periodontology 2008;38(1):83-90
PURPOSE: This study investigated the osteoconductivity of natural calcium carbonate-derived bone substitutes, hen eggshell (ES), and compared with those of commercial bone substitutes. MATERIALS AND METHODS: Osseous defects created in the rat calvaria were filled with particulated ES(ES-1), ES with calcium-deficient hydroxyapatite surface layer (ES-2), Biocoral(Inoteb, France), and Bio-Oss(Geistlich Pharma, Wolhusen, Switzerland). After 4 and 8 weeks of healing, histomorphometic analysis was performed to evaluate the amount of newly formed mineralized bone area (NB%). RESULTS: Histologic and histomorphometric analysis showed new bone formation and direct bony contact with the grafted materials in all groups. At 4 weeks, Biocoral group showed greater NB% compared to Bio-Oss and ES-1 groups (P<0.05). At 8 weeks, Biocoral and ES-2 groups showed significantly greater NB% compared to Bio-Oss group (P<0.05). CONCLUSION: These results indicate that natural calcium carbonate-derived bone substitutes with microporous calciumdeficient hydroxyapatite surface layer may be an effective materials treating osseous defects.
Animals
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Bone Substitutes
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Calcium
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Calcium Carbonate
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Durapatite
;
Minerals
;
Osteogenesis
;
Rats
;
Skull
;
Transplants
9.Chordoid Meningioma: A Case Report.
Je Young YEON ; Jung Il LEE ; Jong Hyun KIM ; Yeon Lim SUH
Journal of Korean Medical Science 2003;18(5):768-771
The term "chordoid meningioma" means meningioma, which is pathologically similar to chordoma, and previously reported that rarely associated with microcytic anemia and/or dysgammaglobulinemia especially in pediatric population. We present a case of this rare variant, which comprises less than 0.5% of all meningiomas. A 33-yr-old man visited our hospital, complaining visual field defect worsening over 7 yr. Neurological examination showed left homonymous hemianopsia. The brain magnetic resonance imaging revealed well enhancing right temporo-occipital mass with cystic portion. Histopathologic findings of resected tumor were compatible with chordoid meningioma which included trabeculae of eosinophilic, vacuolated cells in a myxoid matrix with prominent lymphoplasmacellular infiltration. The neoplastic cells were positive for vimentin and epithelial membrane antigen and negative for glial fibrillary acidic protein and cytokeratin. This is an adult case of chordoid meningioma without anemia or dysgammaglobulinemia.
Adult
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Antigens, CD20/biosynthesis
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Antigens, CD3/biosynthesis
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B-Lymphocytes/pathology
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Brain/pathology
;
Brain Neoplasms/*diagnosis/*pathology
;
CA-15-3 Antigen/biosynthesis
;
Chordoma/*diagnosis/*pathology
;
Human
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Magnetic Resonance Imaging
;
Male
;
Meningeal Neoplasms/*diagnosis
;
Meningioma/*diagnosis
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T-Lymphocytes/pathology
;
Vimentin/biosynthesis
;
Visual Fields
10.A case of poststreptococcal rapidly progressive glomerulonephritis: follow-up renal biopsy.
Suk Yong KIM ; Chul Woo YANG ; Suk Joo AHN ; Je Young WOO ; Eui Jin CHOI ; Byung Kee BANG ; Kwang Sun SUH
Korean Journal of Nephrology 1993;12(1):91-98
No abstract available.
Biopsy*
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Cytoplasm*
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Follow-Up Studies*
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Glomerulonephritis*
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Kidney Transplantation*