Essential thrombocytosis

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Essential thrombocytosis Microchapters
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Overview
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Epidemiology and Demographics
Risk Factors
Screening
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Differentiating Essential thrombocytosis from other Diseases
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Criteria
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
Chest X Ray
CT
MRI
Echocardiography or Ultrasound
Other Imaging Findings
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Medical Therapy
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Essential thrombocythemia, primary thrombocythemia, inherited essential thrombocythemia, inherited Essential thrombocytosis, inherited essential thrombocythaemia, inherited essential thrombocythemia, inherited ET, congenital essential thrombocythemia, congenital essential thrombocytosis, congenital essential thrombocythaemia, congenital essential thrombocythemia, congenital ET, hereditary essential thrombocythemia, hereditary essential thrombocytosis, hereditary essential thrombocythaemia, hereditary essential thrombocythemia, hereditary ET, familial essential thrombocythemia, familial essential thrombocytosis, familial essential thrombocythaemia, familial essential thrombocythemia, familial ET

Diagnosis

History & Symptoms | Physical Examination | Staging | Lab Tests | Electrocardiogram | Chest X Ray | CT | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies | Diagnostic criteria

Treatment

Medical Therapy | Special care related to pregnancy | Surgery | Primary Prevention | Secondary Prevention

Resources

• Cancerbackup Essential Thrombocytosis page
• CMPD Education Foundation
• MPD Foundation and Research Alliance - Register for a free newsletter
• Overview of Agrylin, the tradename for anagrelide hydrochloride

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