Chronic Eosinophilic Leukemia-Not Otherwise Specified (CEL-NOS) - Idiopathic Hypereosinophilic Syndrome (IHES)

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dc.contributor.author Mohamed, Anwar N -
dc.date.accessioned 2019-04-08T11:21:10Z
dc.date.available 2019-04-08T11:21:10Z
dc.date.issued 2019 -
dc.identifier.citation Anwar N, Mohamed. Chronic Eosinophilic Leukemia-Not Otherwise Specified (CEL-NOS) - Idiopathic Hypereosinophilic Syndrome (IHES). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 3, p. 72-75 -
dc.identifier.issn 1768-3262 -
dc.identifier.uri http://hdl.handle.net/2042/70027
dc.description.abstract Chronic eosinophilic leukemia (CEL) not otherwise specified (NOS) and idiopathic hypereosinophilic syndrome (HES) are rare hematologic disorders characterized by chronic, unexplained eosinophilia with manifestation of organ involvement related to eosinophil infiltration, in the absence of evidence of secondary causes such as parasitic infestation, allergy, or neoplasm. Neither CEL-NOS nor idiopathic HES show Ph chromosome/ BCR-ABL fusion gene or other genetically defined entities such as PDGFRA, PDGFRB, or FGFR1 abnormalities. en
dc.language.iso en -
dc.publisher ARMGHM - Atlas Génétique des Cancers -
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org/Anomalies/ChrEosinoLeukID1340.html -
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology en
dc.rights Open access resource - terms and conditions : http://irevues.inist.fr/utilisation -
dc.subject Chronic eosinophilic syndrome en
dc.subject hypereosinophilia en
dc.subject CEL-NOS en
dc.subject idiopathic HES en
dc.subject.classification Leukaemia Section en
dc.title Chronic Eosinophilic Leukemia-Not Otherwise Specified (CEL-NOS) - Idiopathic Hypereosinophilic Syndrome (IHES) en
dc.type Article -
dc.contributor.affiliation Cytogenetics Laboratory, Pathology Department, Detroit Medical Center, Wayne, State University School of Medicine, Detroit, MI USA -
dc.identifier.doi https://doi.org/10.4267/2042/70027


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