Secondary thrombocytosis.

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منابع مشابه

Secondary thrombocytosis

To estimate the incidence and causes of secondary thrombocytosis in children, a 12 month study of all patients attending a children's hospital and discovered to have a platelet count over two times the upper normal limit (>800xlO9//l) was undertaken. Data so obtained were analysed both separately and together with those from two previous studies to gain as broad a perspective as possible. Of 79...

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Secondary thrombocytosis.

To estimate the incidence and causes of secondary thrombocytosis in children, a 12 month study of all patients attending a children's hospital and discovered to have a platelet count over two times the upper normal limit (> 800 x 10(9)/l) was undertaken. Data so obtained were analysed both separately and together with those from two previous studies to gain as broad a perspective as possible. O...

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Secondary Thrombocytosis in Children

Secondary thrombocytosis is defined as a growth of platelet number over 440.000/mm3 or more than 2 standard deviations, secondary to a primary disease like iron deficiency anemia or an infection. It is frequently observed in children, especially in infants and young children, often randomly discovered. There are few data published on the incidence and the significance of secondary thrombocytosi...

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Cholestatic Hepatitis and Thrombocytosis in a Secondary Syphilis Patient

The incidence of acute hepatitis in syphilis patient is rare. First of all, our patient presented with hepatitis comorbid with thrombocytosis. To our knowledge, this is only the second report of syphilitic hepatitis with thrombocytosis. The 42-yr-old male complained of flu-like symptoms and skin eruptions on his palms and soles. Laboratory findings suggested an acute hepatitis and thrombocytosi...

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Thrombocytosis.

Major progress in understanding the pathogenesis in patients with thrombocytosis has been made by identifying mutations in the key regulators of thrombopoietin: the thrombopoietin receptor MPL and JAK2. Together, these mutations can be found in 50% to 60% of patients with essential thrombocythemia or primary myelofibrosis and in 10% to 20% of hereditary thrombocytosis. A decrease in expression ...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1993

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.68.1.88