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특발성 IgM 단일클론성 감마글로불린병증 1 예

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Author(s)
박근용권석룡권오종서승연송홍석전동석
Keimyung Author(s)
Jeon, Dong SeokPark, Keun YongSong, Hong Suk
Department
Dept. of Laboratory Medicine (진단검사의학)
Dept. of Internal Medicine (내과학)
Journal Title
대한내과학회지
Issued Date
1987
Volume
33
Issue
6
Abstract
A 66-year-old fanner was admitted with dizziness and dyspnea on exertion. The peripheral blood showed hematocrit of 8.4gm/dl with microcytic hypochromic anemia, serum iron of 26 /zg/dl, total iron binding capacity of 316 /ig/'dl, and ferritin of 1.64 ng/ml. The bone marrow smear revealed normal cellularity with 4:1 of myeloid/erythroid ratio, 2.9% of plasmacytosis with normal morphology, and no stainable iron. Protein electrophoresis revealed prominent monoclonal gammopathy in gamma-fraction and arc of IgM-kappa type in both serum and 'irine. After observation of 1 year with iron supplementation, M-component of serum and urine is increased 33% and 71% from initial value. This case is 1st case of idiopathic IgM monoclonal gammopathy in korea which associated with iron deficiency anemia, and regular examination is needed whether the disorder is progression to the lympho-proliferative malignancy.
Alternative Title
A Case of Idiopathic IgM - Monoclonal Gammopathy and Iron Deficiency Anemia
Keimyung Author(s)(Kor)
전동석
박근용
송홍석
Publisher
School of Medicine
Citation
박근용 et al. (1987). 특발성 IgM 단일클론성 감마글로불린병증 1 예. 대한내과학회지, 33(6), 838–844.
Type
Article
ISSN
1226-329x
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/37803
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
1. School of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학)
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