Zboraș Iulia, Ungureanu Loredana, Șenilă Simona, Petrushev Bobe, Zamfir Paula, Crișan Doinița, Zaharie Flaviu Andrei, Vesa Ștefan Cristian, Cosgarea Rodica
Department of Dermatology, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400006 Cluj-Napoca, Romania.
Department of Pathology, Regional Institute of Gastroenterology and Hepatology, 400162 Cluj-Napoca, Romania.
Diagnostics (Basel). 2024 Sep 12;14(18):2015. doi: 10.3390/diagnostics14182015.
PRAME (PReferentially expressed Antigen in Melanoma) immunohistochemistry has proven helpful in distinguishing malignant from benign melanocytic tumors. We studied PRAME IHC expression in 46 thin melanomas and 39 melanocytic nevi, mostly dysplastic nevi. Twenty-six percent (26.09%) of the melanomas showed diffuse PRAME staining in over 76% of the tumor cells (4+), and 34.78% of the melanomas showed PRAME expression in over 51% of the tumor cells (3+ or 4+), while 8% were entirely negative for PRAME. No melanocytic nevi were PRAME 4+ or 3+. More than half of the nevi (64%) were entirely negative for PRAME staining, and 36% of the nevi showed staining expression in 1-25% (1+) or 26-50% of the cells (2+). No nevi were stained with a color intensity of 3, while 16.67% of the melanomas were stained with this color intensity. Most nevi (78.57%) were stained with an intensity of 1. With a lower positivity threshold, sensitivity increases with still reasonable specificity. The best accuracy was obtained for the 2+ positivity threshold. In conclusion, PRAME staining helps distinguish thin melanomas from dysplastic nevi. However, the threshold of positivity should be lowered in order not to miss thin melanomas.
黑色素瘤优先表达抗原(PRAME)免疫组化已被证明有助于区分恶性和良性黑素细胞肿瘤。我们研究了46例薄型黑色素瘤和39例黑素细胞痣(大多为发育异常痣)中的PRAME免疫组化表达情况。26%(26.09%)的黑色素瘤在超过76%的肿瘤细胞中显示弥漫性PRAME染色(4+),34.78%的黑色素瘤在超过51%的肿瘤细胞中显示PRAME表达(3+或4+),而8%的黑色素瘤PRAME完全阴性。没有黑素细胞痣为PRAME 4+或3+。超过一半的痣(64%)PRAME染色完全阴性,36%的痣在1%-25%(1+)或26%-50%的细胞中显示染色表达(2+)。没有痣的染色强度为3,而16.67%的黑色素瘤染色强度为3。大多数痣(78.57%)的染色强度为1。阳性阈值越低,敏感性增加而特异性仍合理。2+阳性阈值的准确性最佳。总之,PRAME染色有助于区分薄型黑色素瘤和发育异常痣。然而,为了不遗漏薄型黑色素瘤,应降低阳性阈值。