MelanoSITE™: Genetic Analysis for Ambiguous Melanocytic LesionsMelanoSITE is a four-probe FISH assay that enhances diagnostic discrimination between nevi and melanoma. FISH analysis enables rapid, cost-effective insight into genetic abnormalities that characterize progression to malignancy in many lesions. Using a published algorithm that focuses on four chromosome regions most predictive of malignancy1 and internally validated cut-offs, MelanoSITE provides 84% sensitivity and 98% specificity in identification of melanoma.2 This molecular technique expands on traditional histologic evaluation and serves as a useful adjunct in resolution of ambiguous cases.3 Dermatopathologists choose the level of service:
Download printable specimen requirements, levels of service, and a sample report. Read more about “FISH as an Effective Diagnostic Tool for the Management of Challenging Melanocytic Lesions" in this 2011 reference article. Contact us to request more information. MelanoSITE Probes
MelanoSITE by FISH reveals the number of four chromosome regions significant in melanoma. A normal cell has two copies of each region targeted by red, green, yellow, or aqua-colored probes. Loci detected by each color probe are shown on the right. Case StudiesNoted dermatopathologist Dr. Artur Zembowicz incorporates MelanoSITE into evaluation of atypical nevi, Spitz tumors, and other melanocytic proliferations. Comprehensive consultations by Dr. Zembowicz with MelanoSITE can be requested through NeoGenomics. Please contact us at customercare@neogenomics.com or 866.776.8907. Over 100 studies from his practice are available for your review. References
MelanoSITE is a registered trademark of NeoGenomics Laboratories, Inc. |
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