• Title/Summary/Keyword: 본태성 혈소판 증다증

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A Case of Essential Thrombocythemia Presenting as Esophageal Varix Bleeding and Multiple Thrombosis (식도정맥류 출혈과 다발성 혈전증으로 발견된 본태성 혈소판 증다증 1예)

  • Yoon, So-Yeon;Choi, Jun-Hyeok;Kang, Sun-Mi;Cho, Jung-Nam;Bae, Sung-Hwa;Ryoo, Hun-Mo
    • Journal of Yeungnam Medical Science
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    • v.28 no.1
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    • pp.99-104
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    • 2011
  • Essential thrombocythemia (ET), a subcategory of chronic myeloproliferative disorder, is characterized by absolute thrombocytosis due to excessive clonal proliferation of platelets, hyperaggregability of platelets, and increased incidence of thrombosis and hemorrhage. We consider a diagnosis of ET when an unexplained and persistent thrombocytosis is observed. It is difficult to consider ET first when we meet a patient with esophageal varix bleeding or unusual multiple thromboses like mesenteric vein, splenic vein, and portal vein. This article reports a patient who presented initially with esophageal varix bleeding and unusual multiple thromboses, thereafter, she was diagnosed with ET after testing positive for the Janus Tyrosine Kinase 2 (JAK2) V617F mutation. In conclusion, in patients with varix bleeding and unusual multiple thromboses, myeloproliferative disorders like essential thrombocythemia should be considered as a potential cause and testing for the JAK2 mutation is warranted.

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