Skip to main content

Black and Brown Oro-facial Mucocutaneous Neoplasms

Abstract

Black and brown-colored mucocutaneous lesions present a differential diagnostic challenge, with malignant melanoma being the primary clinical concern. The vast majority of pigmented lesions in the head and neck region are the result of benign, reactive factors such as post-inflammatory melanosis. However, it is not uncommon to discover a range of muco-cutaneous black and brown neoplasms in the oro-facial area. The majority of black/brown pigmented neoplasms are melanocytic in origin; these are neoplasms of neural crest derivation. Melanocytic nevi are a diverse group of benign neoplasms that are the result of specific oncogenic mutations. They are common on cutaneous surfaces but can manifest in mucosal sites. Currently, nevi are classified based on clinical and histological criteria. The most common cutaneous and oral mucosal nevus is the acquired melanocytic nevus; nevi do not pose an increased risk for the development of malignant melanoma. Emerging information on specific genetic differences supports the notion of biologically distinct nevi. This article will review the classic clinical and microscopic features of nevi commonly found in the head and neck region, and discuss emerging concepts in nevus pathogenesis and taxonomy. Melanoma is a malignant melanocytic neoplasm and is a result of cumulative genetic deregulation. The etiology of malignant melanoma (MM) is multifactorial and includes underlying genetic susceptibility, UV radiation, skin-type, and race. The majority of MM occurs on cutaneous surfaces and less commonly on mucosal and extra-cutaneous visceral organs. Regardless of location, MM exhibits clinical-pathological features that relate to horizontal or vertical tumor spread. Cutaneous and mucosal MM typically present as asymmetrical, irregularly bordered, large (> 0.5 cm), heterogeneous brown-black lesions with foci of erythema, atrophy or ulceration. As with melanocytic nevi, advances in melanomagenesis research have revealed primary oncogenic BRAF and NRAS mutations associated with cutaneous MM. Unlike their cutaneous counterparts, mucosal melanomas exhibit primary oncogenic alterations in c-KIT and other genes. This article will discuss the role of specific primary oncogenic and secondary/tertiary genetic defects in differential clinical presentation, anatomic distribution, future classification changes, and targeted therapy of melanoma. The clinical and microscopic features of mucosal melanomas and a summary of management guidelines will be discussed. Additionally, this article will cover the salient features of melanocytic neuroectodermal tumor of infancy, a neoplastic entity that can involve the oro-facial region, and the clinical-pathological features of selected, commonly occurring pigmented ectodermally-derived neoplasms that are often part of the clinical differential diagnosis of black–brown pigmented lesions.

This is a preview of subscription content, access via your institution.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

References

  1. Hicks MJ, Flaitz CM. Oral mucosal melanoma: epidemiology and pathobiology. Oral Oncol. 2000;36(2):152–69.

    Article  PubMed  CAS  Google Scholar 

  2. Bastian BC. The molecular pathology of melanoma: an integrated taxonomy of melanocytic neoplasia. Annu Rev Pathol. 2014;9:239–71. https://doi.org/10.1146/annurev-pathol-012513-104658.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  3. Damsky WE, Bosenberg M. Melanocytic nevi and melanoma: unraveling a complex relationship. Oncogene. 2017;36(42):5771–92. https://doi.org/10.1038/onc.2017.189.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  4. Rogers T, Marino ML, Raciti P, Jain M, Busam KJ, Marchetti MA, et al. Biologically distinct subsets of nevi. G Ital Dermatol Venereol. 2016;151(4):365–84.

    PubMed  PubMed Central  Google Scholar 

  5. Krengel S. Nevogenesis–new thoughts regarding a classical problem. Am J Dermatopathol. 2005;27(5):456–65.

    Article  PubMed  Google Scholar 

  6. MacKie RM, English J, Aitchison TC, Fitzsimons CP, Wilson P. The number and distribution of benign pigmented moles (melanocytic naevi) in a healthy British population. Br J Dermatol. 1985;113(2):167–74.

    Article  PubMed  CAS  Google Scholar 

  7. Stegmaier OC. Natural regression of the melanocytic nevus. J Invest Dermatol. 1959;32(3):413–21.

    Article  PubMed  CAS  Google Scholar 

  8. Carrera C, Marghoob AA. Discriminating Nevi from Melanomas: Clues and Pitfalls. Dermatol Clin. 2016;34(4):395–409. https://doi.org/10.1016/j.det.2016.05.003.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  9. Buchner A, Hansen LS. Pigmented nevi of the oral mucosa: a clinicopathologic study of 36 new cases and review of 155 cases from the literature. Part II: analysis of 191 cases. Oral Surg Oral Med Oral Pathol. 1987;63(6):676–82.

    Article  PubMed  CAS  Google Scholar 

  10. Buchner A, Hansen LS. Pigmented nevi of the oral mucosa: a clinicopathologic study of 36 new cases and review of 155 cases from the literature. Part I: a clinicopathologic study of 36 new cases. Oral Surg Oral Med Oral Pathol. 1987;63(5):566–72.

    Article  PubMed  CAS  Google Scholar 

  11. Buchner A, Merrell PW, Carpenter WM. Relative frequency of solitary melanocytic lesions of the oral mucosa. J Oral Pathol Med. 2004;33(9):550–7. https://doi.org/10.1111/j.1600-0714.2004.00238.x.

    Article  PubMed  CAS  Google Scholar 

  12. Ferreira L, Jham B, Assi R, Readinger A, Kessler HP. Oral melanocytic nevi: a clinicopathologic study of 100 cases. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015;120(3):358–67. https://doi.org/10.1016/j.oooo.2015.05.008.

    Article  PubMed  Google Scholar 

  13. Meleti M, Mooi WJ, Casparie MK, van der Waal I. Melanocytic nevi of the oral mucosa—no evidence of increased risk for oral malignant melanoma: an analysis of 119 cases. Oral Oncol. 2007;43(10):976–81. https://doi.org/10.1016/j.oraloncology.2006.11.013.

    Article  PubMed  Google Scholar 

  14. Calonje EB, Lazar T, McKee AP. McKee’s Pathology of the Skin. 4th ed. Elsevier: Saunders; 2012.

  15. Rawal YB, Dodson TB, Bal HS. Oral melanoma: relevance to the dental team members. J Am Dent Assoc. 2017;148(2):113–9. https://doi.org/10.1016/j.adaj.2016.10.005.

    Article  PubMed  Google Scholar 

  16. Ascierto PA, Accorona R, Botti G, Farina D, Fossati P, Gatta G, et al. Mucosal melanoma of the head and neck. Crit Rev Oncol Hematol. 2017;112:136–52. https://doi.org/10.1016/j.critrevonc.2017.01.019.

    Article  PubMed  Google Scholar 

  17. Eisen D, Voorhees JJ. Oral melanoma and other pigmented lesions of the oral cavity. J Am Acad Dermatol. 1991;24(4):527–37.

    Article  PubMed  CAS  Google Scholar 

  18. Femiano F, Lanza A, Buonaiuto C, Gombos F, Di Spirito F, Cirillo N. Oral malignant melanoma: a review of the literature. J Oral Pathol Med. 2008;37(7):383–8. https://doi.org/10.1111/j.1600-0714.2008.00660.x.

    Article  PubMed  Google Scholar 

  19. Bandarchi B, Jabbari CA, Vedadi A, Navab R. Molecular biology of normal melanocytes and melanoma cells. J Clin Pathol. 2013;66(8):644–8. https://doi.org/10.1136/jclinpath-2013-201471.

    Article  PubMed  CAS  Google Scholar 

  20. Sortino-Rachou AM, Cancela Mde C, Voti L, Curado MP. Primary oral melanoma: population-based incidence. Oral Oncol. 2009;45(3):254–8. https://doi.org/10.1016/j.oraloncology.2008.04.015.

    Article  PubMed  Google Scholar 

  21. Tavares TS, Meirelles DP, de Aguiar MCF, Caldeira PC. Pigmented lesions of the oral mucosa: a cross-sectional study of 458 histopathological specimens. Oral Dis. 2018. https://doi.org/10.1111/odi.12924.

    Article  PubMed  Google Scholar 

  22. Del Vecchio M, Di Guardo L, Ascierto PA, Grimaldi AM, Sileni VC, Pigozzo J, et al. Efficacy and safety of ipilimumab 3 mg/kg in patients with pretreated, metastatic, mucosal melanoma. Eur J Cancer. 2014;50(1):121–7. https://doi.org/10.1016/j.ejca.2013.09.007.

    Article  PubMed  CAS  Google Scholar 

  23. Azarisamani A, Petrisor D, Wright J, Ghali GE. Metastatic melanotic neuroectodermal tumor of infancy: report of a case and review of the literature. J Oral Maxillofac Surg. 2016;74(12):2431–40. https://doi.org/10.1016/j.joms.2016.05.028.

    Article  PubMed  Google Scholar 

  24. Gaiger de Oliveira M, Thompson LD, Chaves AC, Rados PV, da Silva Lauxen I, Filho MS. Management of melanotic neuroectodermal tumor of infancy. Ann Diagn Pathol. 2004;8(4):207–12.

    Article  PubMed  Google Scholar 

  25. Rachidi S, Sood AJ, Patel KG, Nguyen SA, Hamilton H, Neville BW, et al. Melanotic neuroectodermal tumor of infancy: a systematic review. J Oral Maxillofac Surg. 2015;73(10):1946–56. https://doi.org/10.1016/j.joms.2015.03.061.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Dr. Justin Finch, Assistant Professor and Director of Clinical Photography in the Department of Dermatology at UCONN Health for kindly permitting use several excellent photographs of head and neck pigmented lesions.

Funding

This article did not receive any funding.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Easwar Natarajan.

Ethics declarations

Conflict of interest

The author declares that he has no conflict of interest.

Ethical Approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Informed Consent

Informed consent was obtained from all individuals whose photographs are used in this article.

Rights and permissions

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Natarajan, E. Black and Brown Oro-facial Mucocutaneous Neoplasms. Head and Neck Pathol 13, 56–70 (2019). https://doi.org/10.1007/s12105-019-01008-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12105-019-01008-2

Keywords