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J Clin Pathol 58:629-633 doi:10.1136/jcp.2004.021733
  • Original article

Lymphoma associated chromosomal abnormalities can easily be detected by FISH on tissue imprints. An underused diagnostic alternative

Table 2

 Characteristics of the probes used

Probes (labelling) Hybridisation loci Anomaly detected Typical FISH pattern
Normal Abnormal Type Sensitivity
Sensitivity for the detection of atypical patterns. D-FISH probes: 6.5% for 2R3G; 2.4% for 1R1G1F; 1% for 2R4G, 4R2G, 3R3G, 3R4G, 4R4G, 1R2G2F, 2R1G2F, 2R2G2F, and 0R0V2F; 0.6% for 8R8G, 1R0G3F, 1R1G3F, 3R3V3F, 2R2V3F, 1R1V6F, 4A4R4V, and 8A8R8V (maximum number of false positive cells in 500 cells scored was 23, 6, 1, and 0, respectively); “breakapart” probe: 0.6% for 1R1G2F (maximum number of false positive cells in 500 cells scored was 0).
A, aqua signal; D-FISH, dual colour dual signal fluorescence in situ hybridisation; F, red/green fusion signal; G, green signal; R, red signal.
IGH (G), BCL2 (R) 14q32, 18q21 t(14;18)(q32;q21) 2R2G 1R1G2F D-FISH 1%
CCND1 (R), IGH (G) 11q13, 14q32 t(11;14)(q13;q32) 2R2G 1R1G2F D-FISH 1%
CEP8 (A), c-MYC (R), IGH (G) 8p11.1–q11.1, 8q24, 14q32 t(8;14)(q24;q32) 2A2R2G 2A1R1G2F D-FISH 1%
BCL6 (F) 3q27 t(3;var)(q27;var) 0R0G2F 1R1G1F Breakapart 4%

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