Journal of Laboratory Physicians (Jan 2009)

IgA Plasma Cell Leukemia

  • Tejinder Singh,
  • C S Premalata,
  • K V Sajeevan,
  • Ankit Jain,
  • Ullas Batra,
  • K S Saini,
  • C T Satheesh,
  • K Govind Babu,
  • D Lokanatha

DOI
https://doi.org/10.4103/0974-2727.44415
Journal volume & issue
Vol. 1, no. 01
pp. 019 – 021

Abstract

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Plasma cell leukemia (PCL) is a rare entity. There are two presentations of PCL, primary or secondary. The primary or de novo form of PCL presents with an acute and rapidly progressive leukemic phase. This form occurs when the patient has no pre-existing multiple myeloma (MM). The secondary form is the most advanced form of MM. The PCL is a rare disorder representing 1‒2% of the diagnosed cases of MM. Median age at presentation is usually above 50 years. The monoclonal protein in patients with PCL may be IgG (50%), IgA (15%), or in rare cases IgD or IgE (6%). We report a case of IgA primary PCL that is very rare. Patient was started on combination therapy with vincristine, adriamycin, and dexamethasone. There was poor response and patient died three months after diagnosis.

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