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경상북도 동해안지역의 B 형간염 표면항원 (表面抗原) 보유율에 관한 연구
김용송(Yong Song Kim),박봉기(Bong Ki Park),박재후(Jae Who Park),배효근(Hoy Kin Bae),김재순(Jae Soon Kim),강현철(Hyung Chul Kang),장귀연(Kwi Ryun Chang),김종구(Joong Ku Kim) 대한소화기학회 1988 대한소화기학회지 Vol.20 No.1
N/A To investigate the distribution of hepatitis B surface antigen (HBsAg) in the Pohang city and its neighbourhood area, surveyed 1334 persons who visited hospital general health screening center for check up. The study was performed by RPHA (693 cases) and EIA method (641 cases) with sera obtained. 1) EIBsAg was detected in 108 persons with the positive rate of 8.1% 2) The positive rate among females (10.55%) was greater than that of males (6.22% ) (p<0.005). 3) The age distribution of occurrence rate was found between 20 and 79 years of age ancl the highest rate was 70 to 79 age group(p<0.01).
송준호(Jun Ho Song),정원재(Won Jae Chung),이진우(Jin Woo Lee),신용운(Yong Woon shin),박재후(Jae Who Park),김준미(Joon Mee Kim) 대한소화기학회 1994 대한소화기학회지 Vol.26 No.4
It has been well known that pancreatic tumors occasionally show incidious symptoms resembling chronic pancreatitis as the first manifestation. However, only a few cases were reported about manifestation like acute pancreatitis, confined to pancreatic adenocarcinoma or metastatic carcinomas and there is no clear descriptive report about pancreatic lymphoma associated with acute pancreatitis. Lymphoma of the pancreas itself is a rare neoplasm compris- ing less than 0.16% of all pancreatic malignancies. It is important to exclude other diseases in early clinical course in spite of its difficulty in differential diagnosis because lymphoma is po- tentially curable with chemotherapy or radiation therapy. We report a case of pancreatic non Hodgkins lymphoma presenting with acute pancreatitis as the first manifestation in 34 year old women. In the case, lymphoma was suspected on the basis of clinical and radiological findings and, after histopat,hologic diagnosis obtained from the specimens of metastatic sites, we stanted chemotherapy(COPBLAM) as anecpirical trial. The response was as good as we expected.(Korean J Gastroenterol 1994; 26: 758 763)
Propylthiouracil 에 의한 중증 재생불량성 빈혈 1 예
문태훈(Tai Hoon Moon),송기산(Kee San Song),김인한(In Han Kim),박재후(Jae Who Park),유혜령(Hey Ryoung Yoon),김진주(Jin Ju Kim) 대한내과학회 1996 대한내과학회지 Vol.50 No.5
Antithyroid drugs are usually listed among agents associated with the development of agranulocytosis, but aplastic anemia rarely follows their use. A 34year-old female was admitted to aur hospital with complaint of easy bruise. Three years before We had been diagnosed as Graves' disease and treated with propylthiouracil(PTU). Investigations were as follows' Hemoglobin 66g/L; hematocrit 19.6%; neutrophils 675/μL; platelets 13,000 /U L; corrected reticulocyte count 0.6%; Bone marrow biopsy showed severe hypocellular marrow. We reported a patient of PTU induced severe aplastic anemia with brief review of the literature.
폐암을 동반한 Angioimmunoblastic Lymphadenopathy with Disproteinemia 1 예
최경희(Kyoung Hi Choi),김종진(Jong Jin Kim),박재후(Jae Who Park),정만홍(Man Hong Jung),박병채(Byung Chae Park),이시래(Si Rhae Lee),천봉권(Bong Kwon Chun),허만하(Man Ha Huh) 대한내과학회 1991 대한내과학회지 Vol.40 No.3
Angioimmunmoblastic lymphadenopathy with disproteinemia (AILD) is a rare lymphoproliferative disorder which is recently described and well characterized clinicopatholgic entity. Malignant transformation, usually to malignant lymphoma, occurs in approximately 20% of patients. The association ot AILD and carcinoma is rare: only 5 cases have been reported in the English literature. The rare association of AILD and carcinoma is probably coincidental; however, the immunological imbalance of AILD could have caused the development of the neoplastic disease. We report here a case of AILD with lung cancer of a 58 year old male patient and review the literature.
림프구성 항원 ( CD19 ) 을 보이는 급성 골수성 백혈병 1 예
문태훈(Tai Hoon Moon),송기산(Kee San Song),김여주(Yeo Joo Kim),이진우(Jin Woo Lee),박재후(Jae Who Park),최성숙(Sung Suk Choi),김진주(Jin Ju Kim) 대한내과학회 1995 대한내과학회지 Vol.49 No.5
Recently, immunophenotypic analysis of leukemic cells have an impact on routine diagnostic screening in hematology laboratories, making a critical contribution to the final diagnosis and playing an useful confirmatory role. However, application of this more sophisticated evaluation has let to several reports describing acute leukemias with characteristics of two or more hematopoietic lineage (mixed-lineage leukemia). A 22 year-old female was admitted to our hospital with complaints of dyspnea and palpitation. The peripheral blood and bone marrow examination showed findings of acute myeloid leukemia. The immunophenotypic analysis showed the positivity of HLA-DR, CD13, CD33 and CD19. We report a patient of lymphoid antigen (CD19) expression in acute myeloid leukemia with brief review of the literature.
Diphenylhydantoin 투여중 발생한 용혈성 빈혈을 동반한 순수 적혈구 형성 부전증 1 예
장동섭(Dong Seob Jang),김순혜(Soon Hye Kim),최민준(Min Joon Choi),인현호(Hyun Ho In),박재후(Jae Who Park),윤혜령(Hye Ryoung Yoon),김진주(Jin Ju Kim) 대한내과학회 1994 대한내과학회지 Vol.46 No.2
Pure red cell aplasia is an uncommon disease characterized by findings of abscence of reticulocytes in the peripheal blood, and abscence of erythroblasts and normal leukocytes and platelet production in the marrow. Its cause and mechanism is obscure but immunologic mechanism is strongly suggested because of the wide variety of immunologic abnormalities and successful treatment with immunosuppressive agents. A 34 year-old female was admitted to our hospital due to general weakness, dizziness and dark-colored urine. She was taking diphenylhydantoin against epilepsy. The peripheral blood smear and bone marrow examination showed normocytic normochromic anemia reticulocytopenia, marked hypoplasia of the erythroid series, and the hematologic and urinary examination showed severe hemolytic evidence. After diphenylhydantoin withdrawal and steroid therapy, the hemolytic anemia and red cell aplasia recovered completely. We are reporting a patient with diphenylhydantoin induced pure red cell aplasia with simultaneous occurrence of hemolytic anemia following administration of diphenylhydantoin with brief review of literature.
황영웅(Young Woong Whang),최병현(Byung Hyun Choi),이내희(Nae Hee Lee),권석호(Suck Ho Kwon),정정일(Jeong Il Jeong),박재후(Jae Who Park),전희선(Hee Sun Jon),박경주(Kyung Joo Park),박광화(Kwang Hwa Park),이강용(Kang Yong Lee),김효철(Hug 대한내과학회 1997 대한내과학회지 Vol.53 No.1
Pulmonary alveolar proteinosis is a rare disease, which hallmark is a dense accumulation of PAS positive phospholipid material within alveolar sac. Pulmonary alveolar proteinosis is classified as primary form of unknown etiology and secondary form associated with other diseases. We report a case of secondary pulmonary alveolar proteinosis associated with acute erythroleukemia. A C year old male patient complained of nonproductive cough and general weakness, and presented fine inspiratory crackles at both lower lung field. Chest radiographs and high resolution CT scans showd a lobular pattern of ground-grass opacity with interlobular septal thickening in the center field of the both lungs, Bone marrow aspiration and biopsy revealed acute erythroleukemia. Open lung biopsy revealed PAS positive eosinophilic granular material filled in alveoli. He was treated with TAD chemotherapy, but died from multiorgan failure with pneumonia 22days after chemotherapy.