| A Case of Hereditary Spherocytosis |
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T.K Park, S.K Whang, D.U Eum |
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Department of Pediatrics, Catholic Medical College |
| 유전성 구상적혈구증 1예 |
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박태규, 황성규, 음두은 |
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가톨릭의과대학 소아과학교실 |
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| Abstract |
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case of hereditary spherocytosis, which has been experienced in a three years old Korean boy at
Holly House Hospital, was presented
This blood disorper, was uncommon among Koran children, and reported several cases
by Son1) Cho2), Kim3) Hong4) in this country.
This case had visited the. episode of vomiting, general weakness, anemie, jaundice, splenomegaly and
showed peripheral blood was findings which was characterized by marked spherocytosis, hypochromia,
microcytosis and polychromatophilia Threetimes of. blood transfusions had improved his general condition
and peripheral findings, spenectomy was postphoned until next hemlolytic crisis.
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