Frontiers in Medicine (May 2018)

Detection of Central Nervous System Infiltration by Myeloid and Lymphoid Hematologic Neoplasms Using Flow Cytometry Analysis: Diagnostic Accuracy Study

  • Laiz Cameirão Bento,
  • Rodolfo Patussi Correia,
  • Anderson Marega Alexandre,
  • Sonia Tsukasa Nosawa,
  • Eduardo de Carvalho Pedro,
  • Andressa da Costa Vaz,
  • Daniela Schimidell,
  • Gustavo Bruniera Peres Fernandes,
  • Gustavo Bruniera Peres Fernandes,
  • Carlos Augusto Senne Duarte,
  • Carlos Augusto Senne Duarte,
  • Rodrigo de Souza Barroso,
  • Nydia Strachman Bacal,
  • Nydia Strachman Bacal

DOI
https://doi.org/10.3389/fmed.2018.00070
Journal volume & issue
Vol. 5

Abstract

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IntroductionInfiltration of the central nervous system (CNS) by hematologic or lymphoid malignant cells can cause extensive neurological damage, be progressive and fatal. However, usually, the cerebrospinal fluid (CSF) has low cellularity and rapid cell degeneration, which can impair cytometry analysis. Storage and transport measures, sample preparation, and staining protocols can interfere with diagnostic accuracy.ObjectiveTo calculate the diagnostic performance of flow cytometry (FC) using a cell stabilizer for sample preservation compared to cytomorphology in the detection of CNS infiltration by lymphoid and hematologic neoplasms.MethodsCell samples from all consecutive patients with suspected infiltration by hematological malignancies evaluated between January 2014 and December 2016 were included. Cases were analyzed by FC using a cell preservation medium and cytomorphology. Sensitivity and specificity were calculated.ResultsFrom 414 CSF samples, 72 had a phenotype compatible with characteristics of infiltration by hematological disease, whereas cytology was positive for 35 cases. FC showed higher sensitivity and specificity when compared to cytomorphology, particularly in cases with cellularity under 5 leukocytes/mm3.ConclusionWe demonstrated that collecting CSF in a medium that preserves the stability of the sample improves accuracy when compared to cytomorphology, particularly in low-volume and low-cellularity samples.

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