Acute Lymphoblastic Leukemia (ALL) Pediatric Profile FeaturedTest Code F PALL Test Synonyms BCR/ABL 9q34 t(9;22), MLL 11q23, TEL/AML1 t(12;21), trisomy 4, trisomy 10, trisomy 17 Associations Acute lymphoblastic leukemia (ALL) Methodology Fluorescence in situ Hybridization (FISH) CPT Codes 88367 x10 - Morphometric analysis, in situ hybridization, automated 88368 x10 - Morphometric analysis, in situ hybridization, manual Turnaround Time 3 days Specimen Requirements
Specimen Stability
Storage & Handling
Causes for Rejection Clotted specimen; Specimen exposed to extreme temperature; Anticoagulant toxic to cells; Insufficient number of cells; Improper fixative Reference Range See report. Description Cytogenetic abnormalities occur in approximately 70% of cases of ALL in adults. Precursor B-cell acute lymphoblastic leukemia (ALL) occur in 85% of children and 20% of adults with acute leukemia. Abnormalities of chromosome number (hypodiploidy, hyperdiploidy) are more common in ALL than in AML. Hyperdiploidy in children with trisomies of chromosomes 4, 10 and 17 is associated with a good prognosis when structural anomalies are absent. Translocation (12;21) is very difficult to observe with conventional cytogenetic techniques. FISH can detect these abnormalities in interphase and metaphase cells. References
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