1.Investigation of renal function test and urinalysis findings onhepatitis B surface antigen positive patients.
Korean Journal of Clinical Pathology 1992;12(1):19-24
No abstract available.
Antigens, Surface*
;
Humans
;
Urinalysis*
2.Investigation of renal function test and urinalysis findings onhepatitis B surface antigen positive patients.
Korean Journal of Clinical Pathology 1993;13(1):19-24
No abstract available.
Antigens, Surface*
;
Humans
;
Urinalysis*
3.Investigation of renal function test and urinalysis findings onhepatitis B surface antigen positive patients.
Korean Journal of Clinical Pathology 1993;13(1):19-24
No abstract available.
Antigens, Surface*
;
Humans
;
Urinalysis*
4.A Case of Dermatomyositis Manifestated by the Paroxysmal Supraventricular Tachycardia.
Young Sun KIM ; Sun Hee MAENG ; Hong Keun CHO ; Si Hoon PARK ; Gil Ja SHIN
Korean Circulation Journal 1997;27(11):1211-1217
Dermatomyositis is a disease of unknown etiology characterized by inflammation and degeneration of skeletal muscles and cutaneous abnormalities. Cardiac involvement in dermatomyositis-polymyositis is thought to be rare. In recent year, however, there has been an increasing number of reports on cardiac abnormalities in adult dermatomyositis and polymyositis due to development of noninvasive diagnostic techniques. Categorically, these abnormalities have included electrocardiographic changes, cardiac arrhythmias, congestive heart failure, coronary artery disease, and pericarditis. A 56-year-old woman was admittied to the Ewha womans University Hospital with dyspnea and palpitation. She was diagnosed as having dermatomyositis and followed up our department of Dermatology. Electrocardiogram showed a paroxysmal supraventricular tachycardia at as rate of 195/min. The patient was treated with 240mg/day verapamil p.o, 60mg/day prednisone p.o, there was marked improvement of symptoms. Systematic study of cardiac function utilizing echocardiography, Holter monitoring, thallium-201-scan, and gated blood pool studies were conducted in five newly diagnosed patients with dematomyositis-polymyositis. A significant elevation of serum CPK-MB is indicative of cardiac involvement. Cardiac involvement is a serious prognostic sign. We report a case with the review of the literature.
Adult
;
Arrhythmias, Cardiac
;
Coronary Artery Disease
;
Dermatology
;
Dermatomyositis*
;
Dyspnea
;
Echocardiography
;
Electrocardiography
;
Electrocardiography, Ambulatory
;
Female
;
Heart Failure
;
Humans
;
Inflammation
;
Middle Aged
;
Muscle, Skeletal
;
Pericarditis
;
Polymyositis
;
Prednisone
;
Prognosis
;
Tachycardia, Supraventricular*
;
Verapamil
5.CD30 (Ber H2) Distribution in Hodgkin's Disease and non-Hodgkin's Lymphoma.
Bong Hee KIM ; Young Hee MAENG ; Ju Hie LEE ; Moon Ho YANG
Korean Journal of Pathology 1994;28(4):381-388
Forty one cases of Hodgkin's disease and non-Hodgkin's lymphomas were immunohisto-chemi-cally studied for the presence of CD30 antigen on the paraffin embedded formaldehyde fixed tissue by using Ber H2(CD30) monoclonal antibody (Dakopatts, diluted l : 20) and avidin biotin peroxidase complex technique seventy five %(6/8) of Hodgkin's lymphoma and 27% (9/33) of non-Hodgkin's lymphomas were CD30 positive. Five of l7 diffuse large cell and immunoblastic lymphoma and one large cell anaplastic lymphoma showed large numbers of CD30 positive cells. Occasional CD30 positive cells were found in one of 2 angiommunoblastic lymphadenopathy-like T cell lymphoma, one of 4 small lymphocytic lymphoma and one unclassified lymphoma. Immunophenotypically l6% of B cell lymphoma and 42% of T cell lymphoma showed CD30 positivity. six cases of Hodgkin's disease except lymphocyte predominance showed positive tumor cells. Our results show that CD30 is more widespread in histologic subtypes of lymphomas and is not specific for the diagnosis of Hodgkin's disease.
6.Malignant Hemangiopericytoma of the Chest Wall.
In Kyu PARK ; Kyung Young CHUNG ; Dae Hyeon MAENG ; Dong Whan SHIN
The Korean Journal of Thoracic and Cardiovascular Surgery 2000;33(10):843-846
Primary hemangiopericytoma of chest wall is very rate and only a few cases have ever been reported. The tumor aries from the capillary pericyte of Zimmerman. It is a highly vascular slow growing tumor which can be calssified as both malignant and benign varieties. We report a case of a 66 year-old man in whom recurrent hemangiopericytoma was treated by complete surgical excision. In October 1993 he had received surgical excision of hemangiopericytoma on posterior chest wall. For more than 6 years after the operation he was in good condition until a recurrent mass was found on the chest X-ray. The patient was discharged 9 days after the operation and is receiving radiotherapy.
Aged
;
Capillaries
;
Hemangiopericytoma*
;
Humans
;
Pericytes
;
Radiotherapy
;
Thoracic Wall*
;
Thorax*
7.Multiple Spinal Intradural Schwannomas in the Absence of Neurofibromatosis Type 2 Manifestations: A Case Report.
Jung Tae KIM ; Jung Nam SUNG ; Bong Jin PARK ; Maeng Ki CHO ; Young Joon KIM
Journal of Korean Neurosurgical Society 2000;29(4):550-554
No abstract available.
Neurilemmoma*
;
Neurofibromatoses*
;
Neurofibromatosis 2*
8.Cloning and Nucleotide Sequence Analysis of HLA - DRA * 0101 and DRB1 * 0405 Alleles.
Kyung Soo HAHM ; Joo Hyun KANG ; Kil Lyong KIM ; Cheol Young MAENG ; Jung Hyun PARK
Korean Journal of Immunology 1997;19(1):17-28
No abstract available.
Alleles*
;
Base Sequence*
;
Clone Cells*
;
Cloning, Organism*
;
HLA-DR Antigens
9.Gastric Lipomatosis.
Journal of Gastric Cancer 2010;10(4):254-258
Gastric lipomatosis is an extremely rare condition. We present a case of a 69-year-old woman admitted with epigastric soreness. Computerized tomography (CT) revealed extrinsically compressing, fat-containing mass lesions on the entire gastric wall of the antrum and body except for the lesser curvature. A subtotal gastrectomy was performed. Pathology findings confirmed a gastric lipomatosis with multiple gastric ulcerations and extensive disruptions of the muscular layers. This case and reports of other gastric lipomatosis cases indicate that CT should be used to characterize large submucosal masses because CT can show the specific nature and extent of the disease. We believe that surgical treatment is the most appropriate treatment for symptomatic gastric lipomatosis that shows extensive gastric involvement, or when there are multiple gastric lipomas.
Aged
;
Female
;
Gastrectomy
;
Humans
;
Lipoma
;
Lipomatosis
;
Stomach Neoplasms
;
Stomach Ulcer
10.Gastric Lipomatosis.
Journal of Gastric Cancer 2010;10(4):254-258
Gastric lipomatosis is an extremely rare condition. We present a case of a 69-year-old woman admitted with epigastric soreness. Computerized tomography (CT) revealed extrinsically compressing, fat-containing mass lesions on the entire gastric wall of the antrum and body except for the lesser curvature. A subtotal gastrectomy was performed. Pathology findings confirmed a gastric lipomatosis with multiple gastric ulcerations and extensive disruptions of the muscular layers. This case and reports of other gastric lipomatosis cases indicate that CT should be used to characterize large submucosal masses because CT can show the specific nature and extent of the disease. We believe that surgical treatment is the most appropriate treatment for symptomatic gastric lipomatosis that shows extensive gastric involvement, or when there are multiple gastric lipomas.
Aged
;
Female
;
Gastrectomy
;
Humans
;
Lipoma
;
Lipomatosis
;
Stomach Neoplasms
;
Stomach Ulcer