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Pheochromocytoma Evaluation #889
Type of Disorder: Family Cancer Syndromes
Typical Presentation: Headache, palpitations, diaphoresis, hypertension
Indications for Testing: Clinical diagnosis of or suspician of Pheochromocytoma (PHEO), family history of PHEO
Disease(s) tested for: Pheochromocytoma
Test Details
Test Code: 889
Profile includes: MEN2 (RET) Evaluation, SDHB DNA Sequencing Test, Von Hippel-Lindau Syndrome (VHL) Evaluation
Informed Consent Required: Yes
Medicare ABN Required: Yes
Technical Information
Utility: Detects mutations in the coding sequences of the VHL, RET and SDHB genes
Methodology: Polymerase Chain reaction (PCR); DNA Sequencing of the entire coding region of the gene.
Reference Value: No mutation detected
Patents: 6,312,890, 5,654,138
CPT Coding
The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
Stacked CPT Code(s): 83891(1), 83898(31), 83904(31), 83909(31), 83912(1)
Shipping Considerations
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Preferred Specimen Requirements
Type: Whole blood
Minimum Volume: 10 mL (Pediatric minimum: 2 mL)
Collection Tube: Lavender top (EDTA)
Stability: Hemolysis may compromise DNA recovery and integrigy after 48 hours
Storage Conditions: For short periods (until shipped) at 4 degrees C
Shipping Conditions: Overnight at room temperature (specimen arrival must be less than 24 hours after collection) Ship Monday through Thursday only
Test Turnaround: 2 - 8 weeks
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