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. Author manuscript; available in PMC: 2024 Jul 25.
Published in final edited form as: Clin Exp Dermatol. 2024 May 21;49(6):584–590. doi: 10.1093/ced/llae005

Table 2.

S100A81 and PRAME immunohistochemistry staining results in nevi and melanoma cases.

Tumor type, n (%) Common nevi (n=56) Dysplastic nevi (n=54) Melanoma in situ (n=58) Melanoma (n=41)
S100A8 staining score: percentage of tumor-associated epidermis stained2
 1: 0–4% 47 (83.9) 42 (77.8) 20 (34.5) 3 (7.3)
 2: 5–25% 8 (14.3) 9 (16.7) 11 (19.0) 7 (17.1)
 3: 26–50% 0 (0.0) 2 (3.7) 6 (10.3) 10 (24.4)
 4: 51%–75% 0 (0.0) 1 (19) 14 (24.1) 8 (19.5)
 5: >75% 1 (1.8) 0 (0.0) 7 (12.1) 13 (31.7)
PRAME staining score: percentage of tumor stained2
 Absent; 0% 49 (87.5) 22 (40.7) 5 (8.6) 1 (2.4)
 Present, focal; <50% 6 (10.7) 19 (35.2) 8 (13.8) 6 (14.6)
 Present, diffuse; >50% 1 (1.8) 13 (24.1) 45 (77.6) 34 (82.9)
S100A8 staining pattern for cases with staining scores ≥2
Predominately nuclear 9 (16.1) 11 (20.4) 23 (39.7) 20 (48.8)
Nuclear + cytoplasmic 0 (0.0) 1 (1.9) 15 (25.9) 18 (43.9)
Not applicable 47 (83.9) 42 (77.8) 20 (34.5) 3 (7.3)
1

S100A8 IHC staining reported in: Kiuru M, Kriner MA, Wong S, et al. High-Plex Spatial RNA Profiling Reveals Cell Type–Specific Biomarker Expression during Melanoma Development. J Invest Dermatol. May 2022;142(5):1401–1412.e20. doi:10.1016/j.jid.2021.06.041

2

A positive staining score was defined as greater than 50% staining.