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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
Copper, Liver Tissue
Test Code13241
CPT Codes
82525
Preferred Specimen
2 cm liver tissue collected with a 22-gauge needle or
1 cm liver tissue collected with an 18-gauge needle submitted in a trace metal-free (royal blue-top) tube
1 cm liver tissue collected with an 18-gauge needle submitted in a trace metal-free (royal blue-top) tube
Patient Preparation
Gadolinium is known to interfere with most metal tests. If gadolinium-containing contrast media has been administered a specimen should not be collected for 96 hours.
Minimum Volume
2 mg
Other Acceptable Specimens
2 mg tissue in paraffin block (Note: if no more than 1 or 2 cuts have been made to it for slides)
Instructions
1. Two mg of liver tissue is required. This is typically a piece of tissue from a 22-gauge needle biopsy at least 2 cm long. If an 18-gauge needle is used, the tissue must be at least 1 cm in length.
2. Any specimen vial other than a Mayo metal-free vial used should be plastic, leached with 10% nitric acid for 2 days, rinsed with redistilled water, and dried in clean air.
Additional information: Paraffin blocks will be returned 3 days after analysis is complete.
2. Any specimen vial other than a Mayo metal-free vial used should be plastic, leached with 10% nitric acid for 2 days, rinsed with redistilled water, and dried in clean air.
Additional information: Paraffin blocks will be returned 3 days after analysis is complete.
Transport Container
See Collection Instructions
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Liver tissue
Room temperature: Unacceptable
Refrigerated: 10 days
Frozen: Unacceptable
Tissue Paraffin block
Room temperature: Indefinitely
Refrigerated: Indefinitely
Frozen: Indefinitely
Room temperature: Unacceptable
Refrigerated: 10 days
Frozen: Unacceptable
Tissue Paraffin block
Room temperature: Indefinitely
Refrigerated: Indefinitely
Frozen: Indefinitely
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability
Methodology
Inductively Coupled Plasma-Mass Spectrometry
FDA Status
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
Setup Schedule
Set up: Mon, Thurs; Report available: 3-6 days
Reference Range
<50 mcg/g dry wt
Clinical Significance
Diagnosing Wilson disease and primary biliary cirrhosis using liver tissue specimens.