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MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature

Essential thrombocythemia (ET) is a clonal bone marrow disease, characterized by increased production of platelets along with other clinical and bone marrow findings. Most patients with ET will have a somatic mutation in one of the known gene locations of JAK2, CALR, or MPL that can upregulate the J...

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Autores principales: Elsayed, Ahmed G., Ranavaya, Aeesha, Jamil, Muhammad Omer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434327/
https://www.ncbi.nlm.nih.gov/pubmed/30996850
http://dx.doi.org/10.4081/hr.2019.7868
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author Elsayed, Ahmed G.
Ranavaya, Aeesha
Jamil, Muhammad Omer
author_facet Elsayed, Ahmed G.
Ranavaya, Aeesha
Jamil, Muhammad Omer
author_sort Elsayed, Ahmed G.
collection PubMed
description Essential thrombocythemia (ET) is a clonal bone marrow disease, characterized by increased production of platelets along with other clinical and bone marrow findings. Most patients with ET will have a somatic mutation in one of the known gene locations of JAK2, CALR, or MPL that can upregulate the JAK-STAT pathway. MPL mutation is present in 5% of cases with the most common mutations being W515L and W515K. In this report we describe 2 cases of patients with clinical and laboratory picture of ET. One patient carried MPLY252H mutation which is previously unreported in the adult population but has been shown to be a gain-of-function mutation. The other patient carried MPL F126fs mutation which is not known to be of clinical importance and has not been previously reported.
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spelling pubmed-64343272019-04-17 MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature Elsayed, Ahmed G. Ranavaya, Aeesha Jamil, Muhammad Omer Hematol Rep Case Report Essential thrombocythemia (ET) is a clonal bone marrow disease, characterized by increased production of platelets along with other clinical and bone marrow findings. Most patients with ET will have a somatic mutation in one of the known gene locations of JAK2, CALR, or MPL that can upregulate the JAK-STAT pathway. MPL mutation is present in 5% of cases with the most common mutations being W515L and W515K. In this report we describe 2 cases of patients with clinical and laboratory picture of ET. One patient carried MPLY252H mutation which is previously unreported in the adult population but has been shown to be a gain-of-function mutation. The other patient carried MPL F126fs mutation which is not known to be of clinical importance and has not been previously reported. PAGEPress Publications, Pavia, Italy 2019-03-12 /pmc/articles/PMC6434327/ /pubmed/30996850 http://dx.doi.org/10.4081/hr.2019.7868 Text en ©Copyright A.G. Elsayed et al., 2019 http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution NonCommercial 4.0 License (CC BY-NC 4.0).
spellingShingle Case Report
Elsayed, Ahmed G.
Ranavaya, Aeesha
Jamil, Muhammad Omer
MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature
title MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature
title_full MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature
title_fullStr MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature
title_full_unstemmed MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature
title_short MPL Y252H anMd PL F126fs mutations in essential thrombocythemia: Case series and review of literature
title_sort mpl y252h anmd pl f126fs mutations in essential thrombocythemia: case series and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434327/
https://www.ncbi.nlm.nih.gov/pubmed/30996850
http://dx.doi.org/10.4081/hr.2019.7868
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