Sign in →

Chromosomes/FISH - Bone Marrow/Leukemic Peripheral Blood

Clinical System Name

Cytogenetics Neoplasia Final Report

Synonyms

CH-NEOP

Bone Marrow Chromosomes

Bone Marrow Karyotype

Bone Marrow Routine Karyotype

Cytogenetics

Karyotype Bone Marrow

Leukemia Karyotype

Leukemia FISH

Neoplasia Karyotype

Neoplasia FISH

Leuk PB Karyotype

Leukemic Peripheral Blood Karyotype

Leukemic Peripheral Blood Chromosomes

Leukemic Peripheral Blood FISH

Description

Bone marrow/leukemic peripheral blood cells are processed and cultured for chromosome analysis and fluorescence in-situ hybridization (FISH) in the diagnosis of leukemia and other hematologic disorders.  A leukemic peripheral blood sample with >5% circulating blasts can be used when a bone marrow sample can not be obtained.

Sample Requirements

Specimen: Bone Marrow (BM) or Leukemic peripheral blood (LPB)

Container(s): Dark Green/Sodium Heparin (no serum separator)

Preferred Vol: BM: 3.0 mL

                        LPB: 5.0 ml

Minimum Vol:  BM: 1.0 mL; no micro collection

                         LPB: 3.0ml; no micro collection 

Note: 

For more detailed information for bone marrow testing, see separate bone marrow aspirate listing. 

 

A bone marrow sample is the preferred sample type for testing.  Collect 1 - 3 mL bone marrow and transfer marrow from syringe to plain green top sodium heparin tube with no gel separator - see above. 

 

A leukemic peripheral blood sample with >5% circulating blasts can be used when a bone marrow sample can not be obtained.  Collect 3 - 5 mL leukemic peripheral blood into a plain green top sodium heparin tube without gel separator. 

 

Keep sample at room temperature and send to the Lab immediately.  Samples received after 3 pm will be set up the following day.

 

Processing Instructions

Reject due to:  n/a - send to lab

Spin: N

Aliquot: N

Temp: RT

Storage location:  Days: Transport specimen, requistion, and labels with other bone marrow samples to 10th floor Cell Markers (station #180).   Eves/Nights: Store specimen with other bone marrow samples, copy of requisition, and labels in the Cell Markers RT box in CPA.

 

Off-site collection - Bone Marrow:  See Bone Marrow Aspirate listing for complete instructions.  'Seattle Children's Bone Marrow (off-site) - Flow, Morphology, Cytogenetics' requisition must be completed by ordering provider.  Specimen must reach Children's Laboratory within 24 hours of collection.  Samples received after 3 pm will be set up the following day.

Stability

Temperature Time
Room temp 24 hours
Refrigerated No
Frozen No

 

Availability

STAT Performed TAT
N Daily Abnormal prelim within 1 week if requested; final in 2-3 weeks

 

Performing Laboratory

Seattle Children's Hospital

Department

 

Department: Cytogenetics Laboratory

Phone number: 206-987-3961

 

Lab Client Services: 206-987-2617, labclientservices@seattlechildrens.org

 

Lab Genetic Counselor: LabGC@seattlechildrens.org

Methodology

Method:  Standard G-band chromosome analysis.

CPT Codes

88237, 88264, 88291

Special Instructions

Test request form should be completed by the ordering physician.  For additional information or consultation call the Cytogenetics Lab at (206) 987-3961.  Evening and night shift: call the Clinical Lab at (206) 987-2102 or the on-call pathologist at (206) 987-2131.

Requisition

Complete & include copy of Clinical Information System (CIS) HemOnc Bone Marrow Requisition (cases to be evaluated by Seattle Children's Pathology) or Hematopoietic Transplant Marrow Requisition (specimens to be evaluated at Seattle Cancer Care Alliance), as appropriate.

 

For specimens collected off-site: complete & include Seattle Childrens Bone Marrow/Malignancy (Off-site collection) - Flow, Morphology, Cytogenetics requisition.  (see 'Bone Marrow Aspirate' listing)

Clinical Utility

Chromosomes contain the thousands of genes in the human genome that direct cellular processes controlling growth, development, and functioning of the human body.  Acquired chromosomal abnormalities including chromosomal gains, losses, and structural abnormalities have all been associated with cancer.  Identification of specific abnormalities by FISH and Karyotype can help with diagnosis of disease, risk stratification, and prognosis.  Abnormalities detected by FISH and karyotype may be used to monitor disease in follow up studies.

Karyotype testing will detect abnormalities in chromosome number, large chromosomal duplications and deletions and other large structural rearrangements. 

 

FISH testing is used for more targeted studies to confirm or rule out specific abnormalities.