Test Code 8PCDD Flow Cytometry - Myeloma / Plasma Cell Dyscrasia Panel (Diagnostic)
Specimen Requirements
Submit one of the following:
Fresh specimen required
(a) Specimen Type: Bone marrow (preferable)
Container/Tube: Lavender Top (EDTA), Green Top (Sodium Heparin)
Volume: 5-10mL
(b) Specimen Type: Peripheral blood
Container/Tube: Lavender Top (EDTA), Green Top (Sodium Heparin)
Volume: 20mL
(c) Specimen Type: Lymph Node / Solid Tumour
Container/Tube: Sterile container with 5mL RPMI 1640 media
Volume: 5mm(3) or larger biopsy
Collection Instructions: Place tissue directly into 5mL RPMI 1640 media after biopsy. Do not leave tissue
to air-dry or fix tissue in formalin.
(Prearrange with Flow Cytometry Laboratory for transport media prior sample collection)
(d) Specimen Type: Body fluid
Container/Tube: Sterile tube with 0.6mL transfix media
Volume: 3-6mL
(Prearrange with Flow Cytometry Laboratory for transport media prior sample collection)
Additional Collection Instructions: All specimens should be shipped to the lab in ambient temperature (18-25oC) within 24-48 hours of collection. Specimen received after 48 hours of collection will nonetheless be processed but results may be compromised. For overseas specimens, avoid shipping on Friday or eve of public holidays.
Reference Interval
See laboratory report
Days and Times Performed
Monday through Friday. 20 working days (STAT 5 days)
Methodology
Flow Cytometry
Service Code
12670
Update
Last updated 22/10/2024
Added new test info
Unacceptable Condition
Specimen Type | |
---|---|
Bone Marrow/Peripheral Blood | Frozen |
Specimen Stability
** Preferred temperatures for storage prior to and during shipping to NUH **
Fresh specimen required
Ambient (Preferred) | 24 hours |
---|---|
Refrigerate | 48 hours |
Testing Laboratory
National University Hospital
Flow Cytometry, 67724016
Useful For
This panel is used to diagnose multiple myeloma, various subtypes of plasma cell dyscrasia and amyloidosis. Patient with characteristic aberrant expressions may be followed up as MRD monitoring.
Test Info
Pre-arrange with Haematology before ordering the test.
This laboratory test has undergone in-house evaluation with appropriate quality assurance and control measures in line with laboratory best practice and accreditation requirements.
Reagent(s) used in this test is/are ordered through HSA’s Special Access Route, which provides interim access without full registration.