Test Directory
| Test Code | ||
| UROVB | ||
| Test Name | ||
| Bladder Cancer FISH, MD Review | ||
| CPT Codes | ||
| 88120TC | ||
| Expected Turnaround Time | ||
| 5 days | ||
| Clinical Utility | ||
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The assay is designed to detect aneuploidy for chromosomes 3, 7, 17, and loss of the 9p21 locus via fluorescence in situ hybridization (FISH) in urine specimens from subjects with transitional cell carcinoma of the bladder. This assay does not detect other chromosomal or genetic alterations. Results are intended for use as a noninvasive method of monitoring for tumor recurrence in conjunction with cystoscopy in patients previously diagnosed with bladder cancer. The clinical interpretation of test results should be evaluated within the context of the patient's medical history and other diagnostic laboratory test results. |
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| Specimen and Container Info | ||
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Specimen Type: Urine
Collection Container: TCC Monitoring kit (Dianon Cytology/Urovysion Collection Kit)
Desired Specimen Volume: 50 mL |
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| Collection Instructions | ||
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| Processing and Submission Instructions | ||
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| Transport Instructions | ||
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Transport to the laboratory refrigerated. |
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| Stability Requirements | ||
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| Causes for Rejection | ||
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| Methodology | ||
| FISH, Fluorescence In-Situ Hybridization | ||
| Reference Intervals | ||
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See patient report. |
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| Limitations | ||
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Positive FISH results in the absence of other signs or symptoms of bladder cancer recurrence may be evidence of other urinary tract-related cancers (eg, ureter, urethra, renal, and/or prostate in males), and further patient follow-up may be helpful. Negative FISH results in the presence of other signs and symptoms of bladder cancer recurrence may need to be regarded as suspicious false-negative results; repeat testing may be indicated. Although the assay was designed to detect chromosome changes associated with most bladder cancers, there are some bladder cancers whose genetic changes are not targeted by this test. Specimens should be received at the laboratory within 72 hours post-collection for optimal testing. Specimens older than 72 hours will not be rejected; however, results are not guaranteed. In these instances, therefore, client should consider recollection if possible. |
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| Alternate Names | ||
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| Reference Lab | ||
| Labcorp Of America Holdings | ||
| Testing Schedule | ||
| Monday-Friday | ||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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