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essential_thrombocytosis [2025/06/19 07:32] – [treatment] gary1essential_thrombocytosis [2026/05/10 19:34] (current) – [introduction] wh
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     * the thrombopoietin gene (THPO)      * the thrombopoietin gene (THPO) 
     * the thrombopoietin receptor gene (MPL) - include MPL-P106L, MPL-S505N (this may increase thrombotic risk), and MPL-W515R, as well as the polymorphism MPL-K39N termed MPL Baltimore     * the thrombopoietin receptor gene (MPL) - include MPL-P106L, MPL-S505N (this may increase thrombotic risk), and MPL-W515R, as well as the polymorphism MPL-K39N termed MPL Baltimore
 +    * possibly POT1 mutation (([[https://ashpublications.org/blood/article/147/19/2226/566170/Lymphoid-malignancy-and-clonality-in-the-POT1|2026: Lymphoid malignancy and clonality in the POT1-mediated long telomere syndrome ]]))
     * JAK2 kinase (V617F) gene - not inherited itself as this is a somatic mutation, but some families have familial predisposition     * JAK2 kinase (V617F) gene - not inherited itself as this is a somatic mutation, but some families have familial predisposition
   *prognosis is much better than for [[myelofibrosis]] with 10 yr survival rates > 90%, and 20 yr survival rates around 75% for JAK-2 or MPL mutations, and ~85% for CALR mutations   *prognosis is much better than for [[myelofibrosis]] with 10 yr survival rates > 90%, and 20 yr survival rates around 75% for JAK-2 or MPL mutations, and ~85% for CALR mutations
essential_thrombocytosis.txt · Last modified: 2026/05/10 19:34 by wh

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