Inherited transmission of the CSF3R T618I mutation: A familial report
| dc.authorid | 0000-0002-2035-9462 | |
| dc.authorid | 0000-0001-9636-4113 | |
| dc.contributor.author | Serin, istemi | |
| dc.contributor.author | Cinli, Tahir Alper | |
| dc.contributor.author | Tunç, Sertaç | |
| dc.contributor.author | Kaynar, Leylagül | |
| dc.contributor.author | Sevindik, Ömür Gökmen | |
| dc.contributor.author | Yokuş, Osman | |
| dc.date.accessioned | 2023-09-25T13:15:18Z | |
| dc.date.available | 2023-09-25T13:15:18Z | |
| dc.date.issued | 2023 | |
| dc.department | İstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalı | |
| dc.description.abstract | To the editor, Chronic neutrophilic leukemia (CNL) is a rare, break cluster region-Abelson 1 (BCR-ABL1) negative myeloproliferative neoplasm, which is characterized by mature neutrophilic proliferation with neutrophilic hyperplasia in bone marrow and hepatosplenomegaly [1]. The disease is frequently diagnosed at an advanced age; therefore, the median age of diagnosis was reported as 66.5 [2]. There are a few features that distinguish CNL from chronic myeloid leukemia (CML), such as more mature granulopoietic forms compared to CML, the preponderance of granulocytes (??80%) at the segmented or band stage of maturation, and minimal to no circulating blasts [1, 2]. Deterioration of thrombocytopenia along with increasing splenomegaly points out disease progression or blastic crisis [2]. | |
| dc.identifier.citation | Serin, İ., Cinli, T. A., Tunç, S., Kaynar, L., Sevindik, Ö. G. ve Yokuş, O. (2023). Inherited transmission of the CSF3R T618I mutation: A familial report. Annals of Hematology, 102(2), 477-479. https://doi.org/10.1007/s00277-022-05050-z | |
| dc.identifier.doi | 10.1007/s00277-022-05050-z | |
| dc.identifier.endpage | 479 | |
| dc.identifier.issn | 0939-5555 | |
| dc.identifier.issn | 1432-0584 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 36376598 | |
| dc.identifier.scopus | 2-s2.0-85141975739 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 477 | |
| dc.identifier.uri | https://doi.org/10.1007/s00277-022-05050-z | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12511/11495 | |
| dc.identifier.volume | 102 | |
| dc.identifier.wos | 000883210200002 | en_US |
| dc.identifier.wosquality | Q2 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.institutionauthor | Kaynar, Leylagül | |
| dc.institutionauthor | Sevindik, Ömür Gökmen | |
| dc.language.iso | en | |
| dc.publisher | Springer | |
| dc.relation.ispartof | Annals of Hematology | en_US |
| dc.relation.publicationcategory | Diğer | |
| dc.rights | info:eu-repo/semantics/embargoedAccess | |
| dc.subject | CSF3R T618I | |
| dc.subject | Mutation | |
| dc.subject | Inherited Transmission | |
| dc.title | Inherited transmission of the CSF3R T618I mutation: A familial report | |
| dc.type | Letter |











