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Quick Review for Patients
Note: click on underlined words for more detail or photos. The oral mucosa is usually not pigmented despite the fact that it has the same density of melanocytes as the skin. Occasional patients, however, will show a focal area of melanin deposition, either as a response to local chronic conditions (mechanical trauma, tobacco smoking, chronic autoimmune mucositis), racial background (the darker a person's skin color the more likely they are to have oral pigmentation), or systemic medications, especially chloroquine. Moreover, certain syndromes and systemic diseases have oral pigmentation as part of their spectrum (Table 1), as mentioned previously in this section. Most focal melanin deposits of the oral mucosa which are not associated with race or an appropriate syndrome are innocuous surface discolorations called oral melanotic macule (focal melanosis). This entity represents not only a focal increase in melanin deposition but a concomitant increase in the number of melanocytes. Unlike the cutaneous ephelis (freckle), the oral melanotic macule is not dependent on sun exposure, nor does it show the elongated rete ridges of actinic lentigo. Some authorities have questioned the purported lack of an association with actinic irradiation for melanotic macule located on the vermilion border, preferring to consider the lesion at this site to be a distinct entity called labial melanotic macule. Melanotic macules are found in the mouths of 1 of every 1,000 adults (Table 2). Clinical Features the oral melanotic macule has a 2:1 female predilection with an average age of 43 years at the time of diagnosis, although it can develop at any age. One-third of lesions occur on the vermilion border of the lower lip, but the buccal mucosa, gingiva and palate are other sites of common occurrence. Almost a fifth of the lesions are multiple. The typical macule is a well-demarcated, uniformly tan to dark brown, asymptomatic, round or oval discoloration less than 7 mm. in diameter (Figure 1). The lesion is not thickened and has the same consistency as surrounding mucosa. It tends to have an abrupt onset and seldom enlarges after diagnosis. A special case of oral melanosis, called smoker's melanosis (Figure 2), is found on the gingival or buccal mucosa in heavy smokers. It has an adult onset and is often associated with a concomitant superficial white/gray keratosis. The keratosis may become thick enough to mimic leukoplakia, although it is not known whether or not it is a true precancer. Both the pigmentation and the keratosis diminish or disappear once the tobacco habit is stopped. While the melanotic macule is an innocuous lesion, it must be remembered that focal oral and oropharyngeal pigmentation might represent an internal malignancy (usually lung), an oral manifestation of a systemic disease or one facet of a genetic syndrome (Table 1). Pathology and Differential Diagnosis The oral melanotic macule is characterized by an otherwise normal stratified squamous epithelium with abundant melanin deposits within the keratinocytes of the basal and parabasal layers (Figures 3 & 4). Deposits may also be seen within subepithelial stroma (melanin incontinence), perhaps within macrophages or melanophages (Figure 5). There is no underlying inflammatory response. The melanin can be distinguished from iron deposits with melanin stains or by the loss of brown color after bleaching. Brown formalin deposits can be differentiated by their association with erythrocytes rather than with basal layer epithelial cells. Treatment and Prognosis No treatment is required for oral melanotic
macule except for esthetic considerations. The intraoral melanotic
macule has no malignant transformation potential, but an early melanoma could
have a similar clinical appearance. For this reason, pigmented macular lesions
of recent onset, large size, irregular pigmentation, unknown duration, or
with a history of recent enlargement should be excised and examined
histopathologically. References (Chronologic Order) Note: For general references click on link to the left.Specific references:Merchant HW, Haynes LE, Ellison LT. Soft-palate pigmentation in lung disease, including cancer. Oral Surg Oral Med Oral Pathol 1976; 41:726-733. Buchner A., Hansen LS. Melanotic macule of the oral mucosa: a clinicopathologic study of 105 cases. Oral Surg Oral Med Oral Pathol 1979; 48: 244-249. Watkins KV, Chaudhry AP, Yamane GM, et al. Benign focal melanotic lesions of the oral mucosa. J Oral Med 1984; 39: 91-96. Brown FH, Houston GD. Smoker's melanosis: a case report. J Periodontol 1991; 62:524-527. Hedin CA, et al. Disappearance of smoker's melanosis after reducing smoking. J Oral Pathol Med 1993; 22:228-230. Ho KK, Dervan P, O'Loughlin S, Powell FC. Labial melanotic macule: a clinical, histopathologic, and ultrastructural study. J Am Acad Dermatol 1993; 28:33-39. Kaugars GE, Heise AP, Riley WT, et al. Oral melanotic macules: a review of 353 cases. Oral Surg Oral Med Oral Pathol 1993; 76: 59-61. Trelles MA, et al. Treatment of melanotic spots in the gingiva by argon laser. J Oral Maxillofac Surg 1993; 51:759-761. Barrett AW, et al. Oral melanotic macules that develop after radiation therapy. Oral Surg Oral Med Oral Pathol 1994; 77:431-434.
Table 2: Gender-specific prevalence rates per 1,000 population for selected oral masses and surface alterations in U.S. adults, ranked by total frequency. Modified from Bouquot JE. Common oral lesions found during a mass screening examination. J Am Dent Assoc 1986; 112:50-57, and Bouquot JE, Gundlach KKH. Oral exophytic lesions in 23,616 white Americans over 35 years of age. Oral Surg Oral Med Oral Pathol 1986; 62:284-291.
* total examined population = 23,616 adults over 35 years of age
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