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KMID : 0366219660010010077
Korean Journal of Hematology
1966 Volume.1 No. 1 p.77 ~ p.80
Primary Hemorrhagic Ttrombocythemia -Report of a Case-
¼­¼ø±Ô(ßïâïÐ¥)/S.K. Suh
ÀÌÀÎÈñ(ì°ìÙý÷)/±è±âÈ«(ÑÑѹûó)/I.H. Lee/K.H. Kim
Abstract
This is a 54 year old Korean merchant who complained of pain and discoloration of
the left fifth toe. Following the sympathectomy, he bled of oozinig type from the
operation wound over the Period if two months and the bleeding ceased spontaneously.
He had two finger breath of hepatomcgaly and a normal spleen. His platelet counts
varied from 995,000 to 3,635,000 for the period of three months. The platelet appeared
normal in size and shape. He had also leucocytosis (14,850¡­27,750), eosinophilia (6-18%)
and mild anemia. Other routine laboratory studios were within normal limits. The bone
marrow was norman and three was neither panmyelosis nor megakaryocytosis on two
occasions. Thromboplastin generation test was normal on two occasions. He has been
doing relatively well and there was no evidence of a granulocytic leukemia or
polycythemia vera during the period of following 3 years.
According to the Ozer's criteria this is a case of primary hemorrhagic
thrombocythemia without a megakaryocytosis in the bone marrow.
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