Essential thrombocytosis

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Essential thrombocytosis Microchapters
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Diagnosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Soujanya Thummathati, MBBS [2]

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

Overview

Essential thrombocytosis (ET) is a rare hematologic disorder characterized by overproduction of platelets in the absence of an underlying disease.Platelets are responsible for hemostasis that is to control bleeding by forming plugs at the site of injury. Though overproduced, the platelets in ET are usually dysfunctional resulting in the vascular complications.

Diagnosis

ET is a diagnosis of exclusion. 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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