Detection of a rare JAK2exon13InDel-mutation in chronic eosinophilic leukemia with bilateral cerebral infarctions and Löffler endocarditis-Reference-Cited by-同舟云学术

Detection of a rare JAK2exon13InDel-mutation in chronic eosinophilic leukemia with bilateral cerebral infarctions and Löffler endocarditis

Published:2023-10-16 Issue:1 Volume:103 Page:363-365
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Eisenach Sven,Zinke Jan,Brämer Dirk,Hartinger Stefanie,Haferlach Torsten,Kreipe Hans-Heinrich,Hammersen Jakob,Hamadanchi Ali,Otto Sylvia,Schulze Paul Christian,Bürckenmeyer Florian,Teichgräber Ulf,Hochhaus Andreas,Witte Otto W.,Günther Albrecht,Schrenk Karin G.^ORCID

Funder

Universitätsklinikum Jena

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00277-023-05490-1.pdf

Reference10 articles.

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2. Patel A, Juskevicius R, Mohan S (2023) Novel JAK2 exon 14 mutations L611S or N622Y in cis with JAK2 V617F are associated with distinct clinical phenotype of polycythemia vera and concurrent eosinophilia. Acta Haematol 146:76–81. https://doi.org/10.1159/000527695

3. Klag T, Schnetzke U, Benz R et al (2012) Lerich´s syndrome and Löffler endocarditis in a 30-year-old patient presenting with hypereosinophilic syndrome. Ann Hematol 91:139–141. https://doi.org/10.1007/s00277-011-1232-1

4. Khoury JD, Solary E, Abla O et al (2022) The 5th edition of the World Health Organization classification of haematolymphoid tumours: myeloid and histiocytic/dendritic neoplasms. Leukemia 36(7):1703–1719. https://doi.org/10.1038/s41375-022-01613-1

5. Ono R, Iwahana T, Kato H et al (2021) Literature reviews of stroke with hypereosinophilic syndrome. IJC Heart Vasc 37:100915. https://doi.org/10.1016/j.ijcha.2021.100915