Abstract

Myelodysplastic syndromes (MDS) are characterized clinically by a hyperproliferative bone marrow and peripheral blood cytopenias because of ineffective hematopoiesis. Clonal in origin, MDS was often thought to represent a preneoplastic or preleukemic state; however, more than half of patients die from complications of MDS without evolving to acute myeloid leukemia (AML). Diagnosis is made by excluding other etiologies of cytopenias, and on morphologic and cytogenetic findings from a bone marrow biopsy, which are used to determine prognosis and treatment. Supportive therapies such as erythropoiesis stimulating agents and transfusions are the mainstay of treatment for low risk MDS, while hypomethylating agents and in some cases stem cell transplant are the first line treatments for patients with high risk disease.

Original languageEnglish
Title of host publicationOncology
Publisherwiley
Pages288-297
Number of pages10
ISBN (Electronic)9781119189596
ISBN (Print)9781119189558
DOIs
StatePublished - 30 Aug 2019

Keywords

  • 5q-syndrome
  • Myelodysplastic syndromes

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