Thrombocytapheresis in Patient with Essential Thrombocythemia: A Case Report
Afra Elhassan, Arwa Alsaud, Mohamed A. Yassin, Mahmood B Aldapt, Lubna Riaz, Firdous Ghori, Aiman Ahmad, Mohammad Abdul-Jaber Abdulla
Abstract
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Afra Elhassan, Arwa Alsaud, Mohamed A. Yassin, Mahmood B Aldapt, Lubna Riaz, Firdous Ghori, Aiman Ahmad, Mohammad Abdul-Jaber Abdulla
Abstract
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Essential thrombocythemia (ET) is one of the myeloproliferative neoplasms, characterized by persistent thrombocytosis, platelets >450,000/μL, and evident clonal abnormalities like JAK2 V617F, MPL, CALR mutation and not fulfilling WHO criteria for MDS, CML, PV, and IDA. Here we report a 24-year-old female who presented with headache and was found to have thrombocytosis with a platelet count of 2,141 × 103/μL, diagnosed as ET as per WHO criteria 2008; she required ICU admission and thrombocytapheresis with a favorable outcome.
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Essential thrombocythemia (ET) is one of the myeloproliferative neoplasms, characterized by persistent thrombocytosis, platelets >450,000/μL, and evident clonal abnormalities like JAK2 V617F, MPL, CALR mutation and not fulfilling WHO criteria for MDS, CML, PV, and IDA. Here we report a 24-year-old female who presented with headache and was found to have thrombocytosis with a platelet count of 2,141 × 103/μL, diagnosed as ET as per WHO criteria 2008; she required ICU admission and thrombocytapheresis with a favorable outcome.
Key concepts: Essential thrombocythemia, Thrombocytosis, Medicine, Plateletpheresis, Anagrelide, Platelet, Internal medicine, Gastroenterology