Volume 36, Issue 6 pp. 628-635
Original Article

Automated quantification of apoptosis in B-cell chronic lymphoproliferative disorders: a prognostic variable obtained with the Cell-Dyn Sapphire (Abbott) automated hematology analyzer

M. Fumi

M. Fumi

Clinical Pathology Laboratory, A.O.R.N ‘G. Rummo’ di Benevento, Benevento, Italy

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D. Martins

D. Martins

Clinical Pathology Laboratory, A.O.R.N ‘G. Rummo’ di Benevento, Benevento, Italy

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Y. Pancione

Y. Pancione

Clinical Pathology Laboratory, A.O.R.N ‘G. Rummo’ di Benevento, Benevento, Italy

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S. Sale

S. Sale

Clinical Pathology Laboratory, A.O.R.N ‘G. Rummo’ di Benevento, Benevento, Italy

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V. Rocco

Corresponding Author

V. Rocco

Clinical Pathology Laboratory, A.O.R.N ‘G. Rummo’ di Benevento, Benevento, Italy

Correspondence:

Dr Vincenzo Rocco, A.O.R.N. ‘G.Rummo’ di Benevento, Laboratorio di Patologia Clinica, via dell'Angelo n.1, 82100, Benevento, Italy.

Tel.: +39082457256; Fax: +39082457256; E-mail: [email protected]

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First published: 02 June 2014
Citations: 2

Summary

Introduction

B-chronic lymphocytic leukemia CLL, a neoplastic clonal disorder with monomorphous small B lymphocytes with scanty cytoplasm and clumped chromatin, can be morphologically differentiated in typical and atypical forms with different prognosis: Smudge cells (Gumprecht's shadows) are one of the well-known features of the typical CLL and are much less inconsistent in other different types CLPD. Abbott Cell-Dyn Sapphire uses the fluorescence after staining with the DNA fluorochrome propidium iodide for the measurement of nucleated red blood cells (NRBCs) and nonviable cells (FL3+ cell fraction): We have studied the possible correlation between presence and number of morphologically identifiable smudge cells on smears and the percentage of nonviable cells produced by Cell-Dyn Sapphire.

Methods

305 blood samples from 224 patients with B-cell lymphoproliferative disorders and 40 healthy blood donors were analyzed by CBC performed by Cell-Dyn Sapphire, peripheral blood smear, and immunophenotype characterization.

Result

FL3+ fraction in CLPD directly correlated with the percentage of smudge cells and is significantly increased in patients with typical B-CLL. This phenomenon is much less evident in patients with atypical/mixed B-CLL and B-NHL.

Conclusion

In small laboratories without FCM and cytogenetic, smudge cells%, can be utilized as a preliminary diagnostic and prognostic tool in differential diagnosis of CLPD.

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