81168 Ccnd1/igh translocation alys
Also known as: CCND1/IGH translocation testing, mantle cell lymphoma detection
Molecular analysis to detect CCND1/IGH translocation, a hallmark chromosomal abnormality in mantle cell lymphoma.
In Plain Language
lymphoma gene test; blood cancer translocation detection
Clinical Context
Used to confirm diagnosis of mantle cell lymphoma and assess prognosis, as CCND1/IGH translocation is present in approximately 95 percent of mantle cell lymphoma cases.
RVU Information
CPT 81168 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81168?
CPT 81168 (Ccnd1/igh translocation alys) is a Pathology & Lab code. Molecular analysis to detect CCND1/IGH translocation, a hallmark chromosomal abnormality in mantle cell lymphoma.
Who uses CPT code 81168?
CPT 81168 is used by Oncology, Pathology, Hematology. Used to confirm diagnosis of mantle cell lymphoma and assess prognosis, as CCND1/IGH translocation is present in approximately 95 percent of mantle cell lymphoma cases.
When is CPT 81168 used?
Used to confirm diagnosis of mantle cell lymphoma and assess prognosis, as CCND1/IGH translocation is present in approximately 95 percent of mantle cell lymphoma cases.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.