Seminars in Hematology
Volume 40, Issue 3 , Pages 196-200, July 2003

Aplastic anemia and pure red cell aplasia associated with large granular lymphocyte leukemia

  • Ronald S. Go

      Affiliations

    • Sections of Hematology and Oncology, Gundersen Lutheran Medical Center, La Crosse, WI, USA
  • ,
  • John A. Lust

      Affiliations

    • Divisions of Hematology and Hematopathology, Mayo Clinic and Foundation, Rochester, MN, USA
  • ,
  • Robert L. Phyliky

      Affiliations

    • *Address correspondence to Robert L. Phyliky, MD, Mayo Clinic, Division of Hematology, 200 First St SW, Rochester, MN 55905, USA
    • Divisions of Hematology and Hematopathology, Mayo Clinic and Foundation, Rochester, MN, USA

Abstract 

Aplastic anemia (AA) and pure red cell aplasia (PRCA) are two of the various types of immune-mediated cytopenias that can be associated with large granular lymphocyte (LGL) leukemia. We review the experience on LGL leukemia-associated AA and PRCA in the published literature. In the setting of LGL leukemia, AA is found rarely, while PRCA is frequent. However, the diagnosis of LGL leukemia in the presence of pancytopenia is very challenging. In general, the clinical findings and treatment outcome are similar to the idiopathic or primary forms of AA and PRCA. Serial trials of immunosuppressive agents usually result in relatively durable remissions. In refractory cases, studies using newer immunosuppressive agents active against T cells and natural killer (NK) cells are necessary. There are many similarities in the currently known pathophysiologic mechanisms among these three disorders. As LGL leukemia is underdiagnosed, it is interesting to speculate that perhaps a significant proportion of idiopathic AA and PRCA may be, in fact, secondary to LGL leukemia.

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 Supported in part by the Gundersen Lutheran Medical Foundation (R.S.G.).

PII: S0037-1963(03)00140-9

Seminars in Hematology
Volume 40, Issue 3 , Pages 196-200, July 2003