Skip to main content

Advertisement

Log in

Benign Alveolar Ridge Keratosis: Clinical and Histopathologic Analysis of 167 Cases

  • Original Paper
  • Published:
Head and Neck Pathology Aims and scope Submit manuscript

Abstract

Benign alveolar ridge keratosis (BARK), the intraoral counterpart of cutaneous lichen simplex chronicus, is a reactive hyperkeratosis caused by trauma or friction that presents as a poorly demarcated white papule or plaque on the keratinized mucosa of the retromolar pad or alveolar ridge mucosa (often edentulous). This is a clinical and histopathologic analysis of BARK including evaluation of p53 expression in selected cases. One hundred and sixty-seven cases of BARK were identified from 2016 to 2017 and 112 (67.1%) occurred in males with a median age of 56 years (range 15–86). The retromolar pad was affected in 107 (64.1%) cases and the edentulous alveolar mucosa in 60 (35.9%) cases, with 17.4% of the cases presenting bilaterally. BARK showed hyperkeratosis often with wedge-shaped hypergranulosis and occasional focal parakeratosis. The epithelium exhibited acanthosis and surface corrugation with tapered rete ridges often interconnected at the tips. The study for p53 performed in 12 cases showed less than 25% nuclear positivity. BARK is a distinct benign clinicopathologic entity caused by friction, which should be clearly distinguished from true leukoplakia, a potentially malignant disorder.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Natarajan E, Woo SB. Benign alveolar ridge keratosis (oral lichen simplex chronicus): a distinct clinicopathologic entity. J Am Acad Dermatol. 2008;58(1):151–7. https://doi.org/10.1016/j.jaad.2007.07.011.

    Article  PubMed  Google Scholar 

  2. Woo S-B. Oral pathology: a comprehensive atlas and text. 2nd ed. Amsterdam: Elsevier; 2016.

    Google Scholar 

  3. Eduardo Calonje SN, Bunker C, Francis N, Chaux A, Cubilla A. McKee’s pathology of the skin, diseases of the anogenital skin. 5th ed. Amsterdam: Elsevier; 2020.

    Google Scholar 

  4. El-Naggar AK, Grandis JR, Takata T, Slootweg P. WHO classification of head and neck tumours. Human Pathol. 2017;66:10–2.

    Article  Google Scholar 

  5. Silverman S Jr, Gorsky M, Lozada F. Oral leukoplakia and malignant transformation. A follow-up study of 257 patients. Cancer. 1984;53(3):563–8.

    Article  Google Scholar 

  6. Lee JJ, Hung HC, Cheng SJ, Chen YJ, Chiang CP, Liu BY, et al. Carcinoma and dysplasia in oral leukoplakias in Taiwan: prevalence and risk factors. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006;101(4):472–80. https://doi.org/10.1016/j.tripleo.2005.07.024.

    Article  PubMed  Google Scholar 

  7. Woo SB, Grammer RL, Lerman MA. Keratosis of unknown significance and leukoplakia: a preliminary study. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(6):713–24. https://doi.org/10.1016/j.oooo.2014.09.016.

    Article  PubMed  Google Scholar 

  8. Reibel J. Prognosis of oral pre-malignant lesions: significance of clinical, histopathological, and molecular biological characteristics. Crit Rev Oral Biol Med. 2003;14(1):47–62.

    Article  Google Scholar 

  9. Liu W, Wang YF, Zhou HW, Shi P, Zhou ZT, Tang GY. Malignant transformation of oral leukoplakia: a retrospective cohort study of 218 Chinese patients. BMC Cancer. 2010;10:685. https://doi.org/10.1186/1471-2407-10-685.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Dost F, Le Cao K, Ford PJ, Ades C, Farah CS. Malignant transformation of oral epithelial dysplasia: a real-world evaluation of histopathologic grading. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;117(3):343–52. https://doi.org/10.1016/j.oooo.2013.09.017.

    Article  CAS  PubMed  Google Scholar 

  11. Wang TY, Chiu YW, Chen YT, Wang YH, Yu HC, Yu CH, et al. Malignant transformation of Taiwanese patients with oral leukoplakia: A nationwide population-based retrospective cohort study. J Formos Med Assoc. 2018;117(5):374–80. https://doi.org/10.1016/j.jfma.2018.01.017.

    Article  PubMed  Google Scholar 

  12. Shearston K, Fateh B, Tai S, Hove D, Farah CS. Malignant transformation rate of oral leukoplakia in an Australian population. J Oral Pathol Med. 2019. https://doi.org/10.1111/jop.12899.

    Article  PubMed  Google Scholar 

  13. Farah CS, Woo SB, Zain RB, Sklavounou A, McCullough MJ, Lingen M. Oral cancer and oral potentially malignant disorders. Int J Dent. 2014;2014:853479. https://doi.org/10.1155/2014/853479.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Martinez J, Georgoff I, Martinez J, Levine AJ. Cellular localization and cell cycle regulation by a temperature-sensitive p53 protein. Genes Dev. 1991;5(2):151–9.

    Article  CAS  Google Scholar 

  15. Jeffers MD, Richmond J, Farquharson M, McNicol AM. p53 immunoreactivity in cervical intraepithelial neoplasia and non-neoplastic cervical squamous epithelium. J Clin Pathol. 1994;47(12):1073–6.

    Article  CAS  Google Scholar 

  16. Jeffreys M, Jeffus SK, Herfs M, Quick CM. Accentuated p53 staining in usual type vulvar dysplasia-a potential diagnostic pitfall. Pathol Res Pract. 2018;214(1):76–9. https://doi.org/10.1016/j.prp.2017.11.009.

    Article  CAS  PubMed  Google Scholar 

  17. Nagao T, Warnakulasuriya S, Sakuma H, Miyabe S, Hasegawa S, Machida J, et al. p53 and ki67 as biomarkers in determining response to chemoprevention for oral leukoplakia. J Oral Pathol Med. 2017;46(5):346–52. https://doi.org/10.1111/jop.12498.

    Article  CAS  PubMed  Google Scholar 

  18. Suwasini S, Chatterjee K, Purkait SK, Samaddar D, Chatterjee A, Kumar M. Expression of P53 protein and Ki-67 antigen in oral leukoplakia with different histopathological grades of epithelial dysplasia. J Int Soc Prev Community Dent. 2018;8(6):513–22. https://doi.org/10.4103/jispcd.JISPCD_241_18.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Nikitakis NG, Rassidakis GZ, Tasoulas J, Gkouveris I, Kamperos G, Daskalopoulos A, et al. Alterations in the expression of DNA damage response-related molecules in potentially preneoplastic oral epithelial lesions. Oral Surg Oral Med Oral Pathol Oral Radiol. 2018;125(6):637–49. https://doi.org/10.1016/j.oooo.2018.03.006.

    Article  PubMed  Google Scholar 

  20. Chi AC, Lambert PR 3rd, Pan Y, Li R, Vo DT, Edwards E, et al. Is alveolar ridge keratosis a true leukoplakia? A clinicopathologic comparison of 2,153 lesions. J Am Dent Assoc. 2007;138(5):641–51.

    Article  Google Scholar 

  21. Bellato L, Martinelli-Klay CP, Martinelli CR, Lombardi T. Alveolar ridge keratosis–a retrospective clinicopathological study. Head Face Med. 2013;9:12. https://doi.org/10.1186/1746-160X-9-12.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Woo SB. Oral epithelial dysplasia and premalignancy. Head Neck Pathol. 2019;13(3):423–39. https://doi.org/10.1007/s12105-019-01020-6.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Villa A, Hanna GJ, Kacew A, Frustino J, Hammerman PS, Woo SB. Oral keratosis of unknown significance shares genomic overlap with oral dysplasia. Oral Dis. 2019. https://doi.org/10.1111/odi.13155.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Pentenero M, Meleti M, Vescovi P, Gandolfo S. Oral proliferative verrucous leucoplakia: are there particular features for such an ambiguous entity? A systematic review. Br J Dermatol. 2014;170(5):1039–47. https://doi.org/10.1111/bjd.12853.

    Article  CAS  PubMed  Google Scholar 

  25. Villa A, Menon RS, Kerr AR, De Abreu AF, Guollo A, Ojeda D, et al. Proliferative leukoplakia: proposed new clinical diagnostic criteria. Oral Dis. 2018;24(5):749–60. https://doi.org/10.1111/odi.12830.

    Article  CAS  PubMed  Google Scholar 

  26. Farah CS, Fox SA. Dysplastic oral leukoplakia is molecularly distinct from leukoplakia without dysplasia. Oral Dis. 2019. https://doi.org/10.1111/odi.13156.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Muller PA, Vousden KH. p53 mutations in cancer. Nat Cell Biol. 2013;15(1):2–8. https://doi.org/10.1038/ncb2641.

    Article  CAS  PubMed  Google Scholar 

Download references

Funding

No funding obtained.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Asma Almazyad.

Ethics declarations

Conflict of interest

No conflict of interest to disclose.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Almazyad, A., Li, CC. & Woo, SB. Benign Alveolar Ridge Keratosis: Clinical and Histopathologic Analysis of 167 Cases. Head and Neck Pathol 14, 915–922 (2020). https://doi.org/10.1007/s12105-020-01151-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12105-020-01151-1

Keywords

Navigation