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1 f 11 patients [45.5%] diagnosed with actinic keratoses).
2 h approximately 30% having 5 or more actinic keratoses.
3 gines or seborrheic keratoses, and 3 actinic keratoses.
4 reduce the rate of new premalignant actinic keratoses.
5 s in human skin SCC and precancerous actinic keratoses.
6 heir premalignant precursor lesions, actinic keratoses.
7 is effective for field treatment of actinic keratoses.
8 n eradicate clinical and subclinical actinic keratoses.
9 melanocytic nevi, blue nevi, and seborrheic keratoses.
10 ell as dysplastic precursor lesions, actinic keratoses.
11 ormalities, pigment dyschromias, and actinic keratoses.
12 ple of 40 skin lesions (8 nevi, 8 seborrheic keratoses, 7 basal cell carcinomas, 7 melanomas, 4 heman
14 es, such as actinic keratoses and seborrheic keratoses, achieving 92% sensitivity and specificity.
17 for identifying transformation-prone actinic keratoses (AKs) and aggressive squamous cell carcinoma (
22 effective in reducing the number of actinic keratoses (AKs) for up to 6 months, but no randomized tr
24 thyl 5-aminolevulinic acid (MAL) for actinic keratoses (AKs) is as effective as conventional photodyn
30 intraepithelial carcinoma including actinic keratoses and Bowen's disease; basal cell carcinoma; ben
35 ancerous skin abnormalities, such as actinic keratoses and seborrheic keratoses, achieving 92% sensit
39 D4+ T cell-mediated immunity against actinic keratoses and, potentially, cancers of the skin and othe
43 five squamous cell carcinomas, five actinic keratoses, and one case of Bowen's disease) and HaCaT an
45 tinocyte carcinomas versus benign seborrheic keratoses; and malignant melanomas versus benign nevi.
48 arcinomas, squamous cell carcinomas, actinic keratoses, atypical nevi, melanocytic nevi, blue nevi, a
49 ed peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads, which we propose
50 in the 5 years prior to enrollment, actinic keratoses count at enrollment, a history of ever use of
51 ciformis keratosis and in some cases actinic keratoses demonstrated similar histology associated with
52 al-cell carcinomas and the number of actinic keratoses during the 12-month intervention period, the n
53 methods are viable ways to evaluate actinic keratoses, even when the investigators differ at differe
54 cancer, seven of 17 (41.2%) dysplastic PUVA keratoses, four of five (80%) skin warts, and four of 12
55 nce of untreated skin malignancy and actinic keratoses in high-risk kidney and liver transplant recip
57 r numbers of keratinocyte cancers or actinic keratoses in immunosuppressed solid-organ transplant rec
59 ikiloderma with Hair abnormalities and Acral Keratoses), in four affected individuals from two UK fam
62 , we randomly assigned patients with actinic keratoses on the face or scalp or on the trunk or extrem
63 ssigned, in a 1:1 ratio, adults with actinic keratoses on the face or scalp to receive either topical
65 entage of reduction in the number of actinic keratoses (primary outcome), local skin reactions, and i
66 for 2 or 3 consecutive days to treat actinic keratoses produced clinically relevant sustained clearan
67 ional profiling of cSCCs adjacent to actinic keratoses reveals TERT promoter and CDKN2A mutations eme
71 those for presumptive skin cancer or actinic keratoses, skin biopsies, or PCP diagnostic accuracy wit
75 ious skin cancer excisions, previous actinic keratoses, smoking status, and height) and 2 statistical
76 pproved for the topical treatment of actinic keratoses, superficial basal cell carcinoma, and genital
77 target genes were activated in some actinic keratoses, the major precancerous lesion in human skin.
80 h intervention period, the number of actinic keratoses until 6 months after randomization, safety, an
83 inoma and basal cell carcinoma), and actinic keratoses was compared between vitiligo cases and contro
85 tly younger, had more nevi but fewer actinic keratoses, were more likely to report a family history o
86 moter and CDKN2A mutations emerge in actinic keratoses, whereas additional mutations that inactivate
87 with premalignant lesions resembling actinic keratoses, whereas those in the heterozygous and wild-ty