Laryngeal keratosis occurs with an estimated annual incidence in the United States of 10.2 lesions per 100 000 males and 2.1 lesions per 100 000 females, respectively.
1 In a single-institution review of laryngeal leukoplakia and a subsequent comprehensive literature review, Isenberg and colleagues
2 found that more than half of these hyperkeratotic vocal fold lesions might not contain dysplasia; however, even lesions that did not contain dysplasia on initial biopsy had a risk of progression to malignant disease. Overall estimates of progression of laryngeal dysplasia to invasive laryngeal cancer vary widely, with estimates as low as 1.7% and as high as 46.3%; a meta-analysis
3 of 940 cases of laryngeal dysplasia revealed a pooled malignant transformation rate of 13.6%, with severe dysplasia and carcinoma in situ having a higher rate of malignant transformation than mild or moderate dysplasia. Genomic analysis on an individual dysplastic lesion might someday allow better prognosis of which particular patients are most at risk of progression to invasive malignant disease,
4 but to date there is no compelling evidence for use of this technology in routine clinical practice.
5