Utility of cell population data to detect myelodysplastic neoplasms in routine laboratory analysis.

Myelodysplastic neoplasms (MDN) are a heterogeneous group of clonal disorders characterised by abnormal production and proliferation of cells within the myeloid cell linage. MDN is more commonly diagnosed in older people and the clinical manifestations vary depending on the severity and specific typ...

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Publicado en:Australian Journal of Medical Science Vol. 46; no. 1; pp. 21 - 31
Autor principal: Gunson, Hanna
Formato: pictorial research tables/charts Journal Article
Publicado: Australian Institute of Medical Scientists Feb2025
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2025
      vid: 46
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      pub: Australian Institute of Medical Scientists
      place: Milton, Queensland, <Blank>
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        atl: Utility of cell population data to detect myelodysplastic neoplasms in routine laboratory analysis.
      aug:
        au: Gunson, Hanna
        affil: Fellowship dissertation Haematology Department, Royal Hobart Hospital, Hobart, Tasmania
      sug:
        subj:
          Myelodysplastic Syndromes Diagnosis
          Hematologic Neoplasms Diagnosis
          Cellular Structures
          Cell Line, Tumor
          Hematologic Tests
          Diagnostic Tests, Routine
          Early Detection of Cancer
          Human
          Middle Age
          Cell Proliferation
          Myeloid Cells
          Consensus
          Disease Progression
          Leukemia, Myeloid, Acute
          Descriptive Statistics
          Middle Aged: 45-64 years
      ab: Myelodysplastic neoplasms (MDN) are a heterogeneous group of clonal disorders characterised by abnormal production and proliferation of cells within the myeloid cell linage. MDN is more commonly diagnosed in older people and the clinical manifestations vary depending on the severity and specific type of the disorder. The disease is often detected during routine blood film examination, triggered by the laboratory review criteria which should be based on the International Consensus group suggested criteria (Barnes et al 2005). While MDN may be slow to progress, progression to acute myeloid leukaemia occurs in approximately 30% of cases (Bejar and Steensma 2014). Early detection of MDN, through triggers outside the Consensus guidelines, may facilitate timely treatment initiation and improve patient outcomes.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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