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KMID : 0366219750100010069
Korean Journal of Hematology
1975 Volume.10 No. 1 p.69 ~ p.73
A Case Report of Hereditary Spherocytosis
ÀÌ¿µ¿Á(ì°çÈè¬)/Y.O. Lee
±èÈ­¼÷(ÑÑûúâ×)/±èµ¿¼ö(ÑÑÔÔâ³)/ÀÌÇÐÁß(ì°ùÊñì)/W.S. Kim/D.S. Kim/H.J. Lee
Abstract
Hereditary spherocytosis seems to be far less frequent in this country than in western
part of the world. Accordingly the reports of hereditary spherocytosis in Korea have
been a few. Recently we had an opportunity to observe a patient, a 22 years old Korean
female, whose clinical, physical, and laboratory finding were consistent with hereditary
spherocytosis. And she was treated with splenectomy with clinical improvement of
jaundice and reddish urine. In addition to the reief of clinical symptoms and signs. there
were improvement in laboratory data such as hemoglobin level, red mass, reticulocyte
count, and bilirubin level etc.
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