Epic Code LAB2111420 PML and RARA t(15;17) by FISH
Test Name Alias
PML and RARA t(15;17) by FISH | 970
Interface Order Alias
11434
Quick Collect
AP Ambient
Clinical Information
Fluorescence in situ hybridization (FISH) using DNA probes for the Promyelocytic Leukemia (PML) Oncogene and the Retinoic Acid Receptor Alpha (RARA) Gene identifies the t(15;17) (q22;q21) in patients with APL and variants of APL. FISH can be done on interphase and metaphase cells, and are useful when routine cytogenetic studies are unsuccessful in locating a submicroscopic PML/RARA fusion. FISH is also useful in monitoring remission in patients with APL.
Routine chromosome analysis is performed on all diagnostic samples and recommended for all bone marrow specimens to exclude abnormalities not identified by the specified FISH probe(s).
Collection Instructions
Multiple specimen collection types. Submit only one.
Specimen Collection: Bone Marrow
Container(s): Green Top (Sodium Heparin)
Preferred volume to collect: 5.0 mL
Minimum volume to collect: 1.0 mL
Neonate volume to collect: 1.0 mL
Collection Instructions:
- Collect bone marrow and transfer marrow from syringe to plain green top sodium heparin tube.
Specimen Collection: Peripheral blood
Container/Tube: Green Top (Sodium Heparin)
Preferred volume to collect: 8.0 mL
Minimum volume to collect: 0.5 mL
Neonate volume to collect: 0.5 mL
Collection Instructions:
- Peripheral blood may be substituted for Bone Marrow if circulating blasts are present
- Collect peripheral blood into a plain green top sodium heparin tube.
- Keep sample at room temperature and send to the Lab immediately.
Processing Instructions (Laboratory, Outpatient or Off-site collection)
Spin: No
Aliquot: No
Transport Temperature: Ambient
If ambient temperature exceeds 80°F or is below 40°F, please send in an insulated container. All samples should be directed to the laboratory as soon as possible.
Specimen Stability
Ambient: 3 days (beyond 3 days, specimen viability will be detemined by Cytogenetics Lab)
Laboratory Retention: primary specimens 4 weeks; frozen pellets retained greater than 1 year
Test Frequency
Test Set Up: Monday – Friday 8:00 am – 5:00 pm, Saturday 8:00 am – 3:00 pm.
Technologist on call for Sunday set up.
Final report: 1 day for initial screening; 2-3 days for follow-up samples.
Reference Range
An interpretive report will be provided.
Performing Department
Cytogenetics
Performing Department Laboratory Location
Corewell Health Advanced Technology Laboratory (ATL), Grand Rapids, MI
Methodology
Performed by fluorescence in situ hybridization (FISH). This test was developed and its performance characteristics determined by Spectrum Health Cytogenetics Laboratory. It has not been cleared or approved by the US FDA. The FDA has determined that such clearance or approval is not necessary. This test is used for clinical purposes.
CPT
88275, 88271 x2
CDM Code
3108827102, 3108827501
Epic Test ID
1230101050
LOINC
Specimen Type: 66746-9
Indication Provided: 42349-1
Result: in process
Interpretation: 59050-5
Comments: 69965-2
Reviewed Date
4/28/2023