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KMID : 0366219860210010099
Korean Journal of Hematology
1986 Volume.21 No. 1 p.99 ~ p.107
Four Cases of Hereditary Spherocytosis
ÁÖ¼ø±â/Soon Ki Joo
±è³²È£/±è¼±Á¤/±èÁ¾È£/À¯°Ç/±è°ü¿±/Nam Ho Kim/Sun Jung Kim/Jong Ho Kim/Gun Yoo/Kwan Yeop Kim
Abstract
Hereditary spherocytosis (H.S.) is a familial hemolytic disorder characterized by
anemia, intermittent jaundice, splenomegaly and uniform responsiveness to splenectomy,
Its morphologic. hallmark is the microspherocyte. This disorder is through to be
inherited as an autosomal dominant trait. Authors have observed 4 cases of
hematologically proven hereditary spherocytosis with family history in Seoul Paik
Hospital during the period of 198B and 1985. Splenectomy was performed in 2 cases
successfully. Both were discharge4 in healthy condition and in good health without any
complication until now. 4 brief review of related literature was also made.
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