Objectives: To evaluate the utility of flow cytometry, karyotype, and a fluorescence in situ hybridization (FISH) panel in screening children for myelodysplastic syndrome (MDS). Methods: Bone marrow morphology, flow cytometry, karyotype, and FISH reports from 595 bone marrow specimens (246 patients) were analyzed. Results: By morphology, 8.7% of cases demonstrated at least unilineage dysplasia and/or increased blasts. Flow cytometry identified definitive abnormalities in 2.8% of cases, all of which had abnormal morphology. Of the 42 cases (7.2%) with acquired karyotypic abnormalities, 26 had no morphologic dysplasia. With a 98.2% concordance between karyotype and MDS FISH, FISH only identified two additional cases, both with low-level (<4%) abnormalities. Peripheral blood count evaluation only identified the absence of thrombocytopenia to correlate with an absence of abnormal ancillary tests. Conclusions: The combination of morphologic evaluation and karyotype with judicious use of flow cytometry and MDS FISH is sufficient to detect abnormalities for these indications.
CITATION STYLE
Chisholm, K. M., Xu, M., Davis, B., Ogi, A., Pacheco, M. C., Geddis, A. E., … Rutledge, J. C. (2018). Evaluation of the Utility of Bone Marrow Morphology and Ancillary Studies in Pediatric Patients under Surveillance for Myelodysplastic Syndrome. American Journal of Clinical Pathology, 149(6), 499–513. https://doi.org/10.1093/ajcp/aqy007
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