查找地点
有关时间、上门服务和预约查找地点
有关时间、上门服务和预约Please direct any questions regarding this test to oncology customer service at 800-345-4363. If reflex test is performed, additional charges/CPT code(s) may apply.
3 - 5 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Bone marrow or peripheral blood
Bone marrow: 2 mL in pediatric green-top (heparin) tube; peripheral blood: 3 mL in pediatric green-top (heparin) tube
Pediatric green-top (heparin) tube
Submit at room temperature using Leukemia/Lymphoma Specimen Transport Kit (supplied by Labcorp). Specimens should arrive in the laboratory within 48 hours of collection. Indicate date and time of collection on the test request form.
Maintain specimen at room temperature.
This test is used to confirm the diagnosis of CML, establish the chronic phase karyotype for comparison with blast crisis alterations and monitor residual disease.
This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.
Cytogenetics; fluorescence in situ hybridization (FISH)
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CPT Statement/Profile Statement
The LOINC® codes are copyright © 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Permission is granted in perpetuity, without payment of license fees or royalties, to use, copy, or distribute the LOINC® codes for any commercial or non-commercial purpose, subject to the terms under the license agreement found at https://loinc.org/license/. Additional information regarding LOINC® codes can be found at LOINC.org, including the LOINC Manual, which can be downloaded at LOINC.org/downloads/files/LOINCManual.pdf