Abstract
Prolymphocytic leukemia (PLL) is a distinct variant of chronic lymphocytic leukemia (CLL) [1, 2]. Although PLL may be suspected in patients with massive splenomegaly and lymphocyte counts over 100 × 109/1, the diagnosis can be made only by identifying the prolymphocyte as the predominant cell in well-prepared peripheral blood films. The typical morphological features of the prolymphocyte—namely, larger size than a normal blood lymphocyte (or CLL) slightly more cytoplasm, and a prominent nucleolus—are best appreciated at ultrastructural level [1, 3–7].
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References
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© 1984 Martinus Nijhoff Publishing, Boston/The Hague/Dordrecht/Lancaster
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Catovsky, D., Matutes, E., Crockard, A.D., O’Brien, M., Costello, C. (1984). Prolymphocytic Leukemia of B- and T-Cell Types. In: Polliack, A. (eds) Human Leukemias. Developments in Oncology Series, vol 14. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2823-0_12
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DOI: https://doi.org/10.1007/978-1-4613-2823-0_12
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