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Test Code MFCDF Myeloma, High Risk with Reflex Probes, Diagnostic FISH Evaluation, Fixed Cell Pellet

Additional Codes

Hospital Order Codex
Lab2608   MISMGO


Ordering Guidance


For the most complete genetic evaluation on fresh bone marrow specimens, order MSMRT/ Mayo Algorithmic Approach for Stratification of Myeloma and Risk-Adapted Therapy Report, Bone Marrow.

 

For evaluation of high-risk abnormalities, with reflex probes, on fresh bone marrow specimens that will be received within 96 hours of collection, order PCPDS / Plasma Cell Proliferative Disorder, High Risk with Reflex Probes, Diagnostic FISH Evaluation, Bone Marrow. If the specimen received for this test is within 96 hours of collection, this test will be canceled and automatically reordered by the laboratory as PCPDS.

 

For testing paraffin-embedded tissue specimens from patients with a plasma cell disorder, order PLASF / Plasma Cell Proliferative Disorder, FISH, Tissue. If the specimen received for this test is paraffin-embedded, this test will be canceled and automatically reordered by the laboratory as PLASF.

 

Fresh bone marrow is only acceptable specimen for this test if the specimen will be received 96 hours or more post-collection.



Shipping Instructions


Advise Express Mail or equivalent if not on courier service.



Necessary Information


1. A list of probes requested for analysis is required if select probes are necessary or if the patient is being tracked for known abnormalities. Probes available for this test are listed in the Testing Algorithm section.

2. A reason for testing must be provided. If this information is not provided, an appropriate indication for testing may be entered by Mayo Clinic Laboratories.

3. A flow cytometry and/or a bone marrow pathology report should be submitted with each specimen. The laboratory will not reject testing if this information is not provided, but appropriate testing and interpretation may be compromised or delayed.



Specimen Required


Container/Tube: Sterile container

Specimen Volume: 1 Fixed cell pellet

Collection Instructions: Place specimen in a sterile container with a 3:1 methanol:glacial acetic acid (or similar) fixative.


Useful For

Detecting, at diagnosis, recurrent high-risk common chromosome abnormalities associated with multiple myeloma or other plasma cell proliferative disorders, when fresh bone marrow is unavailable, using a laboratory-designated probe set algorithm

 

Evaluating specimens in which the bone marrow is past 96 hours from collection

 

This test should not be used to track the progression of disease

Method Name

Fluorescence In Situ Hybridization (FISH)

Reporting Name

Myeloma Fixed Cell, High Risk, FISH

Specimen Type

Fixed Cell Pellet Bone Marrow

Specimen Stability Information

Specimen Type Temperature Time
Fixed Cell Pellet Bone Marrow Ambient (preferred)
  Refrigerated 

Reject Due To

Fresh tissue Reject

Day(s) Performed

Monday through Friday

Report Available

7 to 10 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

88271x6, 88275x3, 88291 x1-FISH Probe, Analysis, Interpretation; 3 probe sets

88271x2, 88275x1-FISH Probe, Analysis; each additional probe set (if appropriate)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
MFCDF Myeloma Fixed Cell, High Risk, FISH In Process

 

Result ID Test Result Name Result LOINC Value
614300 Result Summary 50397-9
614301 Interpretation 69965-2
614302 Result Table 93356-4
614303 Result 62356-1
GC128 Reason for Referral 42349-1
614304 Specimen 31208-2
614305 Source 31208-2
614306 Method 85069-3
614307 Additional Information 48767-8
614308 Disclaimer 62364-5
614309 Released By 18771-6

Forms

If not ordering electronically, complete, print, and send a Hematopathology/Cytogenetics Test Request (T726) with the specimen.