1.Rickets and Glucosuria.
Journal of the Korean Medical Association 2000;43(8):786-790
No abstract available.
Rickets*
2.Significance of Mass Urine Screening in School Children.
Journal of the Korean Medical Association 1998;41(9):949-957
No abstract available.
Child*
;
Humans
;
Mass Screening*
3.Primary Nephrotic Syndrome in Children: A nationwide Survey in Korea.
Journal of the Korean Society of Pediatric Nephrology 1999;3(1):1-10
A case of primary malignant fibrous histiocytoma(MFH) of the lung occurring in a 62-year-old man is presented. After preoperative bronchial brushing and washing cytologic diagnosis of poorly differentiated carcinoma, surgical resection and lymph nodes dissection were performed. Subsequent histologic examination revealed a primary MFH. The diagnosis was confirmed by electron microscopic and immu- nohistochemical examinations. The review of the bronchial brushing and washing cytologic features disclosed many bipolar and a few unipolar spindle tumor cells with a "comet" configuration, mainly single cells, but also forming loose clusters. The nuclei were elongated and hyperchromatic and contained one or more irregular nucleoli. Scattered bizarre, multinucleated tumor giant cells were also present.
Carcinoma, Papillary
;
Child*
;
Diagnosis
;
Giant Cells
;
Humans
;
Korea*
;
Lung
;
Lymph Nodes
;
Middle Aged
;
Nephrotic Syndrome*
;
Thyroid Gland
4.Effect of 1-A ( OH ) D3 on Steroid Induced Bone Loss in Frequently Relapsing Childhood Nephrotic Syndrome.
Byoung Soo CHO ; Deog Yoon KIM
Journal of the Korean Society of Pediatric Nephrology 1997;1(1):13-16
CT guided percutaneous fine-needle aspiration (FNA) of the liver for both cytologic and histologic examination has great value in diagnosing liver malignancy. From March, 1986 to April, 1990, 62 patients with the clinical impression of liver mal- ignancy underwent CT guided percutaneous FNA biopsy. Of these, 43 cases were revi- ewed for this study, 19 were reported to be liver cell carcinoma, 2 were adenocarcinoma, 11 were reported as anaplastic cell present, and the rest (11 cases) were negative (9) or necrotic (2). Among the 11 cases of the last group, 9 were diagnosed as liver cell carcinoma and 2 were necrotic histologically. Retrospective review, in order to clarify the cause of cytologic diagnostic error, of both cytologic and histologic slides of all cases showed discordance of 23% between these diagnoses and sensitivity is 93.9% and specificity is 90.9%. The reasons were as follows ; 1) the lack of awareness of tumor cells of well differentiated liver cell carcinoma (4 cases), 2) missed tumor cells due to too scanty cellularity (1 case), 3) improper smear (2 cases) and no tumor cell in the cytologic smears (3 cases). In such cases, at the initiation of FNA, a correct diagnosis of liver malignancy could only be made by a combination of cytologic and histologic examinations. However after three years' exper- ience we can conclude that cytomorphologic features of liver cell carcinoma are sufficiently distinctive from other liver malignancies to be diagnostic.
Adenocarcinoma
;
Biopsy
;
Biopsy, Fine-Needle
;
Carcinoma, Hepatocellular
;
Diagnosis
;
Diagnostic Errors
;
Humans
;
Liver
;
Nephrotic Syndrome*
;
Retrospective Studies
;
Sensitivity and Specificity
6.Bronchogenic carcinoma manifesting unilateral hyperlucent lung: CT features.
Woo Su CHO ; Kyung Soo LEE ; Byoung Ho LEE
Journal of the Korean Radiological Society 1991;27(3):348-350
No abstract available.
Carcinoma, Bronchogenic*
;
Lung, Hyperlucent*
7.A Case of Primary Fanconi Syndrome.
Byoung Soo CHO ; Hyeonho KANG ; Seong Ho CHA
Journal of the Korean Society of Pediatric Nephrology 1998;2(1):82-85
Meningioma is the most common neoplasm of central nervous system which is hardly diagnosed by cytologic examination. However, preoperative cytologic diagnosis can be easily made in the case of extracranial meningioma, especially in head and neck lesion. We recently experienced a case of fine needle aspiration cytology of meningioma in submandibular area of a 24 year-old male patient. The smear revealed high cellularity in the clean background. Individual tumor cell of nests or syncytium had round or oval nuclei with fine chromatin and moderate amount of lightly stained cytoplasm with indistinct mar- gin. Characteristic cellular whorls, intranuclear inclusions and scattered psammoma bodies made it easy to diagnose a meningioma.
Biopsy, Fine-Needle
;
Carcinoma, Small Cell
;
Central Nervous System
;
Chromatin
;
Cytoplasm
;
Diagnosis
;
Fanconi Syndrome*
;
Giant Cells
;
Head
;
Humans
;
Intranuclear Inclusion Bodies
;
Male
;
Meningioma
;
Neck
;
Salivary Glands
;
Young Adult
8.Clinical Analysis of Mesangial IgM Nephropathy in Childhood.
Joo Hong CHA ; Byoung Soo CHO ; Chang Il AHN
Journal of the Korean Pediatric Society 1986;29(8):50-55
No abstract available.
Immunoglobulin M*
9.A Case of Wiskott-Aldrich Syndrome.
Byoung Geun LEE ; Soo Hee CHANG ; Soo Young CHO ; Pyoung Han HWANG ; Jung Soo KIM
Journal of the Korean Pediatric Society 1994;37(11):1615-1619
Wiskott-Aldrich Syndrome is an X-linked disorder characterized by recurrent infection, thrombocypenia and eczema. Various defects in cell-mediated immunity and deficient antibody reponse to carbohydrate antigens have been described. We experienced a case of Wiskott-Aldrich Syndrome of 28 months old male patient. He has been suffered from multiple petechiae with bleeding, recurrent pyogenic infections and generalized eczema since 3 months of age. Immunological abnormalities are as follows: 1) Serum IgM was gradually decreased, while IgA and IgE were increased. 2) Antibody response against polysaccharide antigen (PRP) was not observed after 3 times of PRPT immunization. 3) CD4/CD8 ratio was reversed (0.6). 4) Proliferative response of mononuclear cells was significantly reduced, and CMI skin test also showed negative results. A brief review of literature was made.
Antibody Formation
;
Child, Preschool
;
Eczema
;
Hemorrhage
;
Humans
;
Immunity, Cellular
;
Immunization
;
Immunoglobulin A
;
Immunoglobulin E
;
Immunoglobulin M
;
Male
;
Purpura
;
Skin Tests
;
Wiskott-Aldrich Syndrome*
10.Three cases of atypical Kawasaki disease with coronary aneurysm.
Min Young PARK ; Kwang Sun HAN ; Sung Yoon CHO ; Byoung Soo CHO ; Sung Ho CHA
Journal of the Korean Pediatric Society 1993;36(9):1315-1319
Kawasaki disease is described by fever lasting five days or more, bilateral conjunctival injection, changes of lips and oral cavity, polymorphous exanthema, acute non-purulent cervical lymphadenopathy, and changes of extremities. Atypical Kawasaki disease is defined as fewer than 4 of 6 criteria described above including coronary artery abnormalities. Especially, atypical clinical manifestations of Kawasaki disease appear in infants younger than 6 months old of age. Thus we recommend echocardiography in early infancy who has prolonged fever in order to diagnose atypical Kawasaki disease and treat early. We have experienced three cases of atypical Kawasaki disease with coronary aneurysm who were admitted because of fever and revealed coronary aneurysm on echocardiography.
Coronary Aneurysm*
;
Coronary Vessels
;
Echocardiography
;
Exanthema
;
Extremities
;
Fever
;
Humans
;
Infant
;
Lip
;
Lymphatic Diseases
;
Mouth
;
Mucocutaneous Lymph Node Syndrome*