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Evolving Concepts in Myelodysplastic Syndromes

  • Azra Raza
Part of the Cancer Treatment and Research book series (CTAR, volume 108)

Abstract

Increasingly in the United States, older individuals between 60 to 75 years of age are discovered as having a variable cytopenia, most commonly detected during a routine visit to the doctor. The clinician's instinctive sense that such low-grade abnormalities would passively loiter coupled with limited therapeutic options led to the non-interventional practice of following these patients with no more than periodic blood counts. In the last two decades, this habit has been replaced by bolder attempts at more precise definitions with the result that the vast majority of such individuals are winding up with a diagnosis of Myelodysplastic Syndrome or MDS. The best proof of this statement is provided by the fact that only 143 patients were recorded as having MDS until 1973 ([Saami & Linman, 1973]), while as many as 10,000 cases are being documented annually at the present time in the United States alone. This dramatic increase in incidence is the result of a combination of factors including an increase in the number of older individuals, aggressive attempts towards a specific diagnosis and probably an increase in the actual incidence of MDS due to toxic and chemical exposure. The exigent imperative for an accurate diagnosis comes first and foremost from an appreciation that MDS is not always a harmless pastiche of benign, poorly defined malaise in hematopoietic cells, but rather can be a deadly, exceedingly pernicious disease capable of killing swiftly.

Keywords

Acute Myeloid Leukemia Acute Leukemia Myelodysplastic Syndrome Acquire Immune Deficiency Syndrome Cytogenetic Abnormality 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 2001

Authors and Affiliations

  • Azra Raza
    • 1
  1. 1.MDS Center and Section of Myeloid Diseases, Department of MedicineRush UniversityChicago

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