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. Author manuscript; available in PMC: 2020 Apr 1.
Published in final edited form as: Am J Dermatopathol. 2019 Apr;41(4):264–272. doi: 10.1097/DAD.0000000000001259

Table 1.

Characteristics of 198 melanocytic specimens analyzed for TERT promoter mutations and classified for diagnosis (melanoma, nevus or diagnostically uncertain melanocytic proliferation) after interobserver review

Characteristic Primary Melanomas (n=86) Nevi (n=72) Uncertain* (n=40)
Number (%) Number (%) Number (%)
Laboratory processing of unstained FFPE tissue sections
 University of North Carolina Pathology Laboratories 81 (94.2) 66 (91.7) 40 (100)
 University of Rochester Pathology Laboratories 5 (5.8) 6 (8.3)
Sex
 Male 55 (64.0) 35 (48.6) 16 (40.0)
 Female 31 (36.1) 37 (51.4) 24 (60.0)
Age at diagnosis of mole or primary melanoma, yrs
 < 65 44 (51.2) 66 (91.7) 35 (87.5)
 ≥ 65 42 (48.8) 6 (8.3) 5 (12.5)
Race
 Whites of European origin 77 (89.5) 50 (69.4) 24 (60.0)
 Other/unknown 9 (10.5) 22 (30.6) 16 (40.0)
Histologic subtype of primary melanoma
 Superficial spreading 43 (50.0)
 Nodular 12 (14.0)
 Lentigo maligna 16 (18.6)
 Acral lentiginous 6 (7.0)
 Other/unclassified 9 (10.5)
Anatomic site of mole or primary melanoma
 Head/neck 28 (32.6) 19 (26.4) 4 (10.0)
 Trunk 27 (31.4) 37 (51.4) 23 (57.5)
 Upper extremities 16 (18.6) 8 (11.1) 2 (5.0)
 Lower extremities 15 (17.4) 8 (11.1) 11 (27.5)
Solar Elastosis adjacent to the melanocytic lesion
 Absent 21 (24.4) 43 (59.7) 34 (85.0)
 Present 59 (68.6) 9 (12.5) 5 (12.5)
 Indeterminate 6 (7.0) 20 (27.8) 1 (2.5)
Contiguous nevus
 Absent 75 (87.2)
 Present 11 (12.8)
Melanocytic nevus type
 Intradermal 17 (23.6)
 Common acquired 9 (12.5)
 Congenital pattern 14 (19.4)
 Dysplastic 14 (19.4)
 Spitz 9 (12.5)
 Other 9 (12.5)
Breslow thickness of primary melanoma, mm
 Median (range) 1.74 (0.37–17.00)
 0.01 to 2.00 45 (52.3)
 > 2.00 41 (47.7)
Ulceration of primary melanoma
 Absent 52 (60.5)
 Present 33 (38.4)
 Indeterminate 1 (1.2)
Mitoses of primary melanoma
 Absent 17 (19.8)
 Present 69 (80.2)
AJCC tumor stage at diagnosis (8th edition)
 1a/1b/2a 38 (44.2)
 2b/3a/3b/4a/4b 48 (55.8)
AJCC overall stage at diagnosis (8th edition)
 IA/IB 34 (39.5)
 IIA/IIB/IIC 19 (22.1)
 IIIA/IIIB/IIIC 25 (29.1)
 IV 3 (3.5)
 Unknown 5 (5.8)
Tumor infiltrating lymphocyte (TIL) grade
 Absent 20 (23.3)
 Present 65 (75.6)
 Indeterminate 1 (1.2)
Pigment of the melanocytic lesion
 Absent 16 (18.6) 12 (16.7) 7 (17.5)
 Present 70 (81.4) 60 (83.3) 33 (82.5)
Regression
 Absent 70 (81.4)
 Present 16 (18.6)
*

Melanocytic proliferations were considered diagnostically uncertain if there was interobserver disagreement between any of 3 dermatopathology readers or the pathology report diagnosis of nevus vs. melanoma or one of the dermatopathogists or pathology report described the specimen as having uncertain diagnosis.

Other types of melanoma include nevoid (n=2), desmoplastic (n=1), spindle cell (n=1), spitzoid (n=1) and unclassified (n=4). All of these were TERT-positive except two of the unclassified melanomas.

Other includes cellular blue nevus (n=2), combined intradermal or sclerotic blue nevus, not cellular (n=1), combined nevus with compound congenital pattern and deep penetrating nevus (n=2), pigmented spindle cell nevus (n=2) and proliferative nodule in congenital pattern nevus (n=2).