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dc.contributor.authorKarakurt, Neslihan
dc.contributor.authorUslu, Ilker
dc.contributor.authorAygun, Canan
dc.contributor.authorAlbayrak, Canan
dc.date.accessioned2020-06-21T12:25:56Z
dc.date.available2020-06-21T12:25:56Z
dc.date.issued2019
dc.identifier.issn0041-4301
dc.identifier.urihttps://doi.org/10.24953/turkjped.2019.05.004
dc.identifier.urihttps://hdl.handle.net/20.500.12712/10601
dc.descriptionWOS: 000518430400004en_US
dc.descriptionPubMed: 32104997en_US
dc.description.abstractNeonates with Down syndrome (DS) may have hematological abnormalities such as polycythemia, thrombocytopenia and transient leukemia (TL). The primary objective of this study was to report the descriptive data of complete blood counts (CBC) of neonates with DS, which were obtained within first week of life. We wanted to focus on neonates with hematological abnormalities and compare them among those with and without TL. The secondary objective was the description of hematological malignancies in the first six years of life. Medical records of 100 neonates with DS between 2006-2018 were assessed. Hematological abnormalities were present in 73/100. We detected anemia in 16, polycythemia in eight, microcytosis in 10, leukopenia in two, leukocytosis in 11, thrombocytopenia in 26, thrombocytosis in 7 and TL in 11 patients. TL group had higher levels of leukocyte count (115.0 +/- 93.0x10(3)/mm(3)) when compared with neonates without TL (11.7 +/- 5.6x10(3)/mm(3)) (p<0.001). No other statistically significant difference between groups for hemoglobin, MCV and platelet count levels was detected. In the follow- up period, two patients developed acute lymphoblastic leukemia, one hemophagocytic lymphohistiocytosis and one Burkitt lymphoma. None of the TL survivors developed myeloid leukemia of Down Syndrome (ML-DS). Thrombocytopenia may be detected frequently in DS and it may not be a part of TL. We suggest that CBC with peripheral blood film should be evaluated for every patient to check for TL and other hematological disturbances. Despite the fact that none of our TL survivors developed overt leukemia (ML-DS), we also suggest that patients with DS be followed due to the risk of developing leukemia.en_US
dc.language.isoengen_US
dc.publisherTurkish J Pediatricsen_US
dc.relation.isversionof10.24953/turkjped.2019.05.004en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDown syndromeen_US
dc.subjecttransient leukemiaen_US
dc.subjectthrombocytopeniaen_US
dc.subjectleukocytosisen_US
dc.titleHematological disturbances in Down syndrome: single centre experience of thirteen years and review of the literatureen_US
dc.typereviewen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume61en_US
dc.identifier.issue5en_US
dc.identifier.startpage664en_US
dc.identifier.endpage670en_US
dc.relation.journalTurkish Journal of Pediatricsen_US
dc.relation.publicationcategoryDiğeren_US


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