Abstract
Despite central nervous system (CNS) prophylactic programs limit leptomeningeal involvement in acute lymphoblastic leukemia (ALL), it can still occur in a restricted percentage of cases. The exact risk rate remains still unknown, and several factors are associated with an increased probability to develop CNS involvement. Among them, Philadelphia (Ph)-positive genotype seems to play a relevant role. Recently, a flow cytometric assay to detect BCR-ABL protein has been developed, but little is known about its possible employment in leptomeningeal disease. Here, we show the miniaturized application of the original assay for BCR-ABL oncoprotein detection in cerebrospinal fluid (CSF) samples.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Diagnosis, Differential
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Flow Cytometry / methods*
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Fusion Proteins, bcr-abl / cerebrospinal fluid*
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Fusion Proteins, bcr-abl / genetics
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Humans
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Immunoassay
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / cerebrospinal fluid
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / complications
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / diagnosis*
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
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Meningeal Neoplasms / cerebrospinal fluid
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Meningeal Neoplasms / complications
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Meningeal Neoplasms / diagnosis*
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Meningeal Neoplasms / genetics
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Philadelphia Chromosome
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Polymerase Chain Reaction
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / cerebrospinal fluid
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / complications
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / diagnosis*
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics
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Sensitivity and Specificity