PMID- 24618603 OWN - NLM STAT- MEDLINE DCOM- 20140626 LR - 20191210 IS - 1532-0979 (Electronic) IS - 0147-5185 (Linking) VI - 38 IP - 6 DP - 2014 Jun TI - Fluorescence in situ hybridization as an ancillary tool in the diagnosis of ambiguous melanocytic neoplasms: a review of 804 cases. PG - 824-31 LID - 10.1097/PAS.0000000000000189 [doi] AB - Previous studies have demonstrated the utility of fluorescence in situ hybridization (FISH) as an ancillary method in the diagnostic workup of histopathologically ambiguous melanocytic neoplasms. A combination of probes targeting 3 loci on chromosome 6 and 1 on 11q has been reported to distinguish unequivocal melanomas and nevi with a sensitivity and specificity of 87% and 96%, respectively. However, information on how FISH should be integrated into routine clinical testing is limited. We report our experience of FISH testing of 804 ambiguous melanocytic lesions performed as part of routine workup at University of California, San Francisco. The main category (47% of all cases) for which FISH testing was requested was Spitz tumors. Other categories included the distinction of possible melanoma from combined nevi (9%), acral or mucosal nevi (9%), Clark/dysplastic nevi (7%), and blue or deep penetrating nevi (6%) and to assess the possibility of nevoid melanoma (4%). Of the ambiguous tumors successfully tested, 88% received a more definitive benign or malignant final diagnosis. Of the 630 cases that tested negative by FISH, the final diagnosis was benign in 489 (78%) cases, ambiguous in 91 cases (14%), and malignant in 50 cases (8%). A positive FISH result was observed in 124 cases, with a final diagnosis of melanoma in 117 (94%). One (1%) FISH-positive case had an equivocal final diagnosis, and 6 (5%) were interpreted, despite the positive FISH result, as melanocytic nevi. We conclude that FISH testing can help reduce the number of equivocal diagnoses in ambiguous melanocytic neoplasms, in particular if FISH testing is positive, and discuss the challenges and limitations of FISH in clinical practice. FAU - North, Jeffrey P AU - North JP AD - Departments of *Pathology daggerDermatology double daggerThe Helen Diller Comprehensive Cancer Center, University of California, San Francisco, CA. FAU - Garrido, Maria C AU - Garrido MC FAU - Kolaitis, Nicholas A AU - Kolaitis NA FAU - LeBoit, Philip E AU - LeBoit PE FAU - McCalmont, Timothy H AU - McCalmont TH FAU - Bastian, Boris C AU - Bastian BC LA - eng GR - R01-CA131524/CA/NCI NIH HHS/United States PT - Evaluation Study PT - Journal Article PT - Research Support, N.I.H., Extramural PL - United States TA - Am J Surg Pathol JT - The American journal of surgical pathology JID - 7707904 SB - IM MH - Adolescent MH - Aged MH - *Chromosomes, Human, Pair 11 MH - *Chromosomes, Human, Pair 6 MH - Cluster Analysis MH - Female MH - Genetic Predisposition to Disease MH - Humans MH - *In Situ Hybridization, Fluorescence MH - Male MH - *Melanocytes/pathology MH - Middle Aged MH - Nevus, Epithelioid and Spindle Cell/*genetics/pathology MH - Predictive Value of Tests MH - Prognosis MH - San Francisco MH - Skin Neoplasms/*genetics/pathology EDAT- 2014/03/13 06:00 MHDA- 2014/06/27 06:00 CRDT- 2014/03/13 06:00 PHST- 2014/03/13 06:00 [entrez] PHST- 2014/03/13 06:00 [pubmed] PHST- 2014/06/27 06:00 [medline] AID - 10.1097/PAS.0000000000000189 [doi] PST - ppublish SO - Am J Surg Pathol. 2014 Jun;38(6):824-31. doi: 10.1097/PAS.0000000000000189.