eMedicine Specialties > Dermatology > Diseases of the Oral Mucosa

Oral Malignant Melanoma: Follow-up

Author: Bobby Collins II, DDS, MS, Associate Professor of Oral and Maxillofacial Pathology, Department of Diagnostic Sciences, University of Pittsburgh School of Dental Medicine
Coauthor(s): E Leon Barnes Jr, MD, Professor of Pathology and Professor of Otolaryngology, University of Pittsburgh School of Medicine; John Abernethy, MD, Winston-Salem, North Carolina
Contributor Information and Disclosures

Updated: Mar 21, 2008

Follow-up

Further Inpatient Care

  • Diagnosis and subsequent surgical excision of oral melanoma requires lifelong follow-up.
  • Early discussions of potential problems with function, prostheses, oral fungal infection, and lesion recurrence may ensure patient compliance.

Further Outpatient Care

  • Periodic follow-up for oral examination and assessment is necessary to evaluate for recurrence. Perform a thorough oral examination and imaging studies regularly for the life of the patient. Recurrence is described as long as 11 years after the initial surgery.
  • At follow-up visits, dental care, nutritional status, and difficulties with the prosthesis (if necessary) can be addressed. Patient comfort and function are assessed. Treatment or the follow-up schedule can be modified.

Deterrence/Prevention

  • While preventive strategies for cutaneous melanoma are well known, no such strategies for oral malignant melanoma are known.
  • Encourage patients to perform a thorough oral self-examination and to report any abnormal findings to their dentist or physician. Oral lesions that are pigmented, bleed, and have mass should be evaluated early.
  • The most significant findings with self-examination are pigmentary changes; however, masses, ulcers, plaques, and altered sensation also are suggestive of malignant melanoma.

Complications

  • Complications stem from the loss of anatomic structure as a result of the surgical procedure.
    • The loss can result in prolonged or compromised healing, and the need for tissue grafting or prosthesis fabrication.
    • Grafts can fail, and prostheses can irritate mucosa and supporting tissues.
    • Xerostomia (ie, oral dryness), hypernasal speech, and increased incidence of oral fungal infections are possible effects of surgical treatment.
  • INF-A use is associated with malaise, flulike symptoms, fever, and myalgia.
  • Patient education and scheduled follow-up visits can minimize the postoperative complications.

Prognosis

  • The prognosis for patients with oral malignant melanoma is poor, with the 5-year survival rate at 11-18%.
    • Early recognition and treatment greatly improves the prognosis.
    • Late discovery and diagnosis often indicate the existence of an extensive tumor with metastasis.
    • After surgical ablation, recurrence and metastasis are frequent events, and most patients die of the disease in 2 years.
    • A review of the literature indicates that the 5-year survival rate within a broad range of 4.5-48%, but a large cluster occurs at 10-25%.
  • The best option for survival is the prevention of metastasis by surgical excision of any recurrent tumor.
  • Eneroth and Lundberg9 state that patients are not cured of oral melanoma and that the risk of death always exists. Long periods of remission may be punctuated by sudden and silent recurrence.

Patient Education

  • Teach the patient how to perform an effective oral examination.
    • All oral mucosal surfaces available for inspection should be visualized.
    • This examination requires a bit of dexterity and head movement to reflect light appropriately.
    • Adequate oral examination requires good lighting, a mouth mirror, and a 2 X 2-in gauze sponge (and a bathroom mirror for self-inspection).
    • The tongue is retracted and moved from side to side with the 2 X 2-in gauze to achieve an unobstructed view.
  • Healthcare practitioners can reinforce this practice at follow-up appointments and ask patients to demonstrate their skill.

Miscellaneous

Medicolegal Pitfalls

  • Misdiagnosis and the failure to diagnose are most commonly associated with nonpigmented oral malignant melanomas.
  • Clinically, a lesion may be mistaken for a benign pigmented lesion, a reactive process, or an anatomic variation.
    • This mistake can be made especially when the examination is cursory or performed by healthcare providers who are unfamiliar with oral examination.
    • The best advice is to perform a systematic and thorough examination.
  • Histologically, amelanotic melanomas require the use of special stains, because of the pathologic mimics. Appropriate immunohistochemical stains or panels can be used to distinguish possible considerations such as lymphoid, epithelial, and neuroendocrine lesions.

Special Concerns

  • Historically, oral malignant melanoma was reported to progress more rapidly in pregnant females for unknown reasons. This finding was refuted by Borden,10 who reiterated that the only reliable prognostic indicator is the stage of the disease at diagnosis and not pregnancy.
  • Medical therapy and radiation therapy are necessarily curtailed during pregnancy; however, those treatments usually are not an issue in patients with oral malignant melanoma.
  • Surgery during pregnancy is problematic because of the requirements for anesthesia and analgesics.
  • The consideration of pregnancy termination or therapeutic abortion is not clearly justified. The decision must rest with the parents, obstetrician-gynecologist, and surgeon responsible for treating the malignancy.
 


More on Oral Malignant Melanoma

Overview: Oral Malignant Melanoma
Differential Diagnoses & Workup: Oral Malignant Melanoma
Treatment & Medication: Oral Malignant Melanoma
Follow-up: Oral Malignant Melanoma
Multimedia: Oral Malignant Melanoma
References

References

  1. Elder DE, Clark WH Jr, Elenitsas R, Guerry D 4th, Halpern AC. The early and intermediate precursor lesions of tumor progression in the melanocytic system: common acquired nevi and atypical (dysplastic) nevi. Semin Diagn Pathol. Feb 1993;10(1):18-35. [Medline].

  2. Hicks MJ, Flaitz CM. Oral mucosal melanoma: epidemiology and pathobiology. Oral Oncol. Mar 2000;36(2):152-69. [Medline].

  3. Tanaka N, Amagasa T, Iwaki H, Shioda S, Takeda M, Ohashi K, et al. Oral malignant melanoma in Japan. Oral Surg Oral Med Oral Pathol. Jul 1994;78(1):81-90. [Medline].

  4. Prasad ML, Patel SG, Huvos AG, Shah JP, Busam KJ. Primary mucosal melanoma of the head and neck: a proposal for microstaging localized, Stage I (lymph node-negative) tumors. Cancer. Apr 15 2004;100(8):1657-64. [Medline].

  5. Patel SG, Prasad ML, Escrig M, Singh B, Shaha AR, Kraus DH, et al. Primary mucosal malignant melanoma of the head and neck. Head Neck. Mar 2002;24(3):247-57. [Medline].

  6. McKinnon JG, Kokal WA, Neifeld JP, Kay S. Natural history and treatment of mucosal melanoma. J Surg Oncol. Aug 1989;41(4):222-5. [Medline].

  7. Trotti A, Peters LJ. Role of radiotherapy in the primary management of mucosal melanoma of the head and neck. Semin Surg Oncol. May-Jun 1993;9(3):246-50. [Medline].

  8. Kirkwood JM, Ibrahim JG, Sosman JA, Sondak VK, Agarwala SS, Ernstoff MS, et al. High-dose interferon alfa-2b significantly prolongs relapse-free and overall survival compared with the GM2-KLH/QS-21 vaccine in patients with resected stage IIB-III melanoma: results of intergroup trial E1694/S9512/C509801. J Clin Oncol. May 1 2001;19(9):2370-80. [Medline].

  9. Eneroth CM, Lundberg C. Mucosal malignant melanomas of the head and neck with special reference to cases having a prolonged clinical course. Acta Otolaryngol. Nov-Dec 1975;80(5-6):452-8. [Medline].

  10. Borden EC. Melanoma and pregnancy. Semin Oncol. Dec 2000;27(6):654-6. [Medline].

  11. Barker BF, Carpenter WM, Daniels TE, Kahn MA, Leider AS, Lozada-Nur F, et al. Oral mucosal melanomas: the WESTOP Banff workshop proceedings. Western Society of Teachers of Oral Pathology. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. Jun 1997;83(6):672-9. [Medline].

  12. Eisen D, Voorhees JJ. Oral melanoma and other pigmented lesions of the oral cavity. J Am Acad Dermatol. Apr 1991;24(4):527-37. [Medline].

  13. Kroon BB, Nieweg OE. Management of malignant melanoma. Ann Chir Gynaecol. 2000;89(3):242-50. [Medline].

  14. Prasad ML, Patel S, Hoshaw-Woodard S, Escrig M, Shah JP, Huvos AG, et al. Prognostic factors for malignant melanoma of the squamous mucosa of the head and neck. Am J Surg Pathol. Jul 2002;26(7):883-92. [Medline].

Further Reading

Keywords

oral melanoma, oral mucosal melanoma

Contributor Information and Disclosures

Author

Bobby Collins II, DDS, MS, Associate Professor of Oral and Maxillofacial Pathology, Department of Diagnostic Sciences, University of Pittsburgh School of Dental Medicine
Bobby Collins II, DDS, MS is a member of the following medical societies: American Academy of Oral and Maxillofacial Pathology and American Dental Association
Disclosure: Nothing to disclose.

Coauthor(s)

E Leon Barnes Jr, MD, Professor of Pathology and Professor of Otolaryngology, University of Pittsburgh School of Medicine
E Leon Barnes Jr, MD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Association for the Advancement of Science, American Society for Head and Neck Surgery, American Society of Clinical Pathologists, College of American Pathologists, International Academy of Pathology, New York Academy of Sciences, and North American Skull Base Society
Disclosure: Nothing to disclose.

John Abernethy, MD, Winston-Salem, North Carolina
John Abernethy, MD is a member of the following medical societies: American Society of Clinical Pathologists, American Society of Dermatopathology, College of American Pathologists, and United States and Canadian Academy of Pathology
Disclosure: Nothing to disclose.

Medical Editor

Peter Fritsch, MD, Chair, Department of Dermatology and Venereology, University of Innsbruck, Austria
Peter Fritsch, MD is a member of the following medical societies: American Dermatological Association, International Society of Pediatric Dermatology, and Society for Investigative Dermatology
Disclosure: Nothing to disclose.

Pharmacy Editor

Michael J Wells, MD, Associate Professor, Department of Dermatology, Texas Tech University Health Sciences Center
Michael J Wells, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Medical Association, and Texas Medical Association
Disclosure: Nothing to disclose.

Managing Editor

Drore Eisen, MD, DDS, Consulting Staff, Department of Dermatology, Dermatology Research Associates of Cincinnati
Drore Eisen, MD, DDS is a member of the following medical societies: American Academy of Dermatology, American Academy of Oral Medicine, and American Dental Association
Disclosure: Nothing to disclose.

CME Editor

Glen H Crawford, MD, Assistant Clinical Professor, Department of Dermatology, University of Pennsylvania School of Medicine; Chief, Division of Dermatology, The Pennsylvania Hospital
Glen H Crawford, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Medical Association, Phi Beta Kappa, and Society of USAF Flight Surgeons
Disclosure: Nothing to disclose.

Chief Editor

William D James, MD, Paul R Gross Professor of Dermatology, University of Pennsylvania School of Medicine; Vice-Chair, Program Director, Department of Dermatology, University of Pennsylvania Health System
William D James, MD is a member of the following medical societies: American Academy of Dermatology and Society for Investigative Dermatology
Disclosure: elsevier Royalty Other; american college of physicians Honoraria Other

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