Ann Dermatol.  2011 Aug;23(3):276-281. 10.5021/ad.2011.23.3.276.

Subclinical Infiltration of Basal Cell Carcinoma in Asian Patients: Assessment after Mohs Micrographic Surgery

Affiliations
  • 1Department of Dermatology, Cheongju St. Mary's Hospital, Cheongju, Korea.
  • 2Department of Dermatology, College of Medicine, Korea University, Seoul, Korea. kumcihk@korea.ac.kr

Abstract

BACKGROUND
Several differences in basal cell carcinomas (BCCs) were found, according to the ethnic group; for example, pigmented BCCs was more common in Asian or Hispanic patients. However, there are few reports on the subclinical extension of the BCC in Asian patients.
OBJECTIVE
The aim of this study was to evaluate the subclinical infiltration of the basal cell carcinoma in Asian patients.
METHODS
All patients with BCC who visited the department of dermatology at Korea University Ansan Hospital were treated with Mohs micrographic surgery. In 81 patients, 83 tumors of BCC were completely eradicated by Mohs micrographic surgery (MMS) from April 2001 to August 2008, and were reviewed in this study. Information recorded included the total margin and the number of stages of Mohs micrographic surgery, anatomic location, tumor size, presence of pigmentation, clinical type, and pathological subtype. We divided the clinical types into nodular, ulcerated, and pigmented, and the pathological types into nodular, micronodular, morpheaform, and adenoid. The BCC was of pigmented type if pigmentation covered more than 25% of the tumor, regardless of whether pigmentation was distinct, or if there was apparent pigmentation that covered more than 10% of the tumor.
RESULTS
The nose and cheek were the most common sites requiring more than one stage of surgery. In tumors smaller than 1 cm, 91.7% required only one stage of excision, compared with 60.6% in tumors larger than 1 cm. More than two Mohs stages were required in 25% of non-ulcerated BCCs and in 46.2% of ulcerated BCCs. Sixty eight percent of pigmented BCCs required only one stage of Mohs micrographic surgery. In cases of non-pigmented BCCs, only 45% required one Mohs stage. More than one Mohs stage was required in 19.2% of non-aggressive BCCs and in 42.9% of aggressive BCCs.
CONCLUSION
Subclinical infiltration differed between the two groups according to the size of the BCC (1 cm threshold) and most of the BCCs were located in the head and neck area. Considering this result, indication for MMS can be extended for BCCs larger than 1 cm in Asian patients. Ulcerated BCCs required more Mohs stages than non-ulcerated BCCs. Pigmented BCCs might show lesser subclinical infiltration than non-pigmented BCCs. Aggressive pathological subtypes showed more subclinical infiltration than the non-aggressive types; however, after evaluation of the border that was excised with MMS, mixed histologic types were found to be more frequent than generally accepted. Therefore, we consider that, when planning surgery, dermatologists should not place too much confidence in the pathologic subtypes identified by biopsy.

Keyword

Basal cell carcinoma; Mohs surgery; Pigmentation; Subclinical infiltration

MeSH Terms

Adenoids
Asian Continental Ancestry Group
Biopsy
Carcinoma, Basal Cell
Cheek
Dermatology
Head
Hispanic Americans
Humans
Hypogonadism
Korea
Mitochondrial Diseases
Mohs Surgery
Neck
Nose
Ophthalmoplegia
Pigmentation
Ulcer
Hypogonadism
Mitochondrial Diseases
Ophthalmoplegia

Figure

  • Fig. 1 Mohs stage according to the size of the basal cell carcinoma.

  • Fig. 2 Pathologic subtypes of basal cell carcinoma according to pigmentation. Nod: nodular, Mor: morpheaform, Mic: micronodular, Ade: adenoid.

  • Fig. 3 (A, B) Basal cell carcinomas (BCCs) requiring only one Mohs stage for complete excision. They showed even pigmentation. (C, D) BCCs requiring more than one Mohs stage for complete excision. They also showed even pigmentation; however, there was a bluish hue surrounding the tumors.


Reference

1. Song ES, Cho BK, Kim SY, Kim SN, Suh KS, Son SJ, et al. A clinicopathological study of basal cell carcinoma in Korean patients. Korean J Dermatol. 2000. 38:762–771.
2. Ishihara K, Saida T, Otsuka F, Yamazaki N. Prognosis and Statistical Investigation Committee of the Japanese Skin Cancer Society. Statistical profiles of malignant melanoma and other skin cancers in Japan: 2007 update. Int J Clin Oncol. 2008. 13:33–41.
Article
3. Kikuchi A, Shimizu H, Nishikawa T. Clinical histopathological characteristics of basal cell carcinoma in Japanese patients. Arch Dermatol. 1996. 132:320–324.
Article
4. Bigler C, Feldman J, Hall E, Padilla RS. Pigmented basal cell carcinoma in Hispanics. J Am Acad Dermatol. 1996. 34:751–752.
Article
5. Kim EJ, Yun SJ, Lee JB, Kim SJ, Won YH, Lee SC. A clinicopathological study of facial basal cell carcinoma treated by Mohs micrographic surgery. Korean J Dermatol. 2006. 44:721–726.
6. Leibovitch I, Huilgol SC, Selva D, Richards S, Paver R. Basal cell carcinoma treated with Mohs surgery in Australia I. Experience over 10 years. J Am Acad Dermatol. 2005. 53:445–451.
Article
7. Smeets NW, Kuijpers DI, Nelemans P, Ostertag JU, Verhaegh ME, Krekels GA, et al. Mohs' micrographic surgery for treatment of basal cell carcinoma of the face--results of a retrospective study and review of the literature. Br J Dermatol. 2004. 151:141–147.
Article
8. Bhatti AZ, Asif S, Alwan M. Factors affecting incomplete excision of nonmelanoma skin cancers in New Zealand. Ann Plast Surg. 2006. 57:513–516.
Article
9. Bøgelund FS, Philipsen PA, Gniadecki R. Factors affecting the recurrence rate of basal cell carcinoma. Acta Derm Venereol. 2007. 87:330–334.
Article
10. Kumar P, Watson S, Brain AN, Davenport PJ, McWilliam LJ, Banerjee SS, et al. Incomplete excision of basal cell carcinoma: a prospective multicentre audit. Br J Plast Surg. 2002. 55:616–622.
Article
11. Telfer NR, Colver GB, Morton CA. British Association of Dermatologists. Guidelines for the management of basal cell carcinoma. Br J Dermatol. 2008. 159:35–48.
Article
12. Sterry W. European Dermatology Forum Guideline Committee. Guidelines: the management of basal cell carcinoma. Eur J Dermatol. 2006. 16:467–475.
13. Netscher DT, Spira M. Basal cell carcinoma: an overview of tumor biology and treatment. Plast Reconstr Surg. 2004. 113:74e–94e.
Article
14. Carucci JA, Leffell DJ. Wolff K, Goldsmith LA, Katz SI, Gilchrest BA, Paller AS, Leffell DJ, editors. Basal cell carcinoma. Fitzpatrick's dermatology in general medicine. 2008. 7th ed. New York: McGraw-Hill;1036–1042.
15. Batra RS, Kelley LC. Predictors of extensive subclinical spread in nonmelanoma skin cancer treated with Mohs micrographic surgery. Arch Dermatol. 2002. 138:1043–1051.
Article
16. National Comprehensive Cancer Network. Basal cell and squamous cell skin cancers. NCCN Clinical Practice Guidelines in Oncology. 2009.
17. Hsuan JD, Harrad RA, Potts MJ, Collins C. Small margin excision of periocular basal cell carcinoma: 5 year results. Br J Ophthalmol. 2004. 88:358–360.
Article
18. Kimyai-Asadi A, Alam M, Goldberg LH, Peterson SR, Silapunt S, Jih MH. Efficacy of narrow-margin excision of well-demarcated primary facial basal cell carcinomas. J Am Acad Dermatol. 2005. 53:464–468.
Article
19. Tan WP, Tan AW, Ee HL, Kumarasinghe P, Tan SH. Melanization in basal cell carcinomas: microscopic characterization of clinically pigmented and non-pigmented tumours. Australas J Dermatol. 2008. 49:202–206.
Article
20. Maloney ME, Jones DB, Sexton FM. Pigmented basal cell carcinoma: investigation of 70 cases. J Am Acad Dermatol. 1992. 27:74–78.
Article
21. Betti R, Gualandri L, Cerri A, Inselvini E, Crosti C. Clinical features and histologic pattern analysis of pigmented basal cell carcinomas in an Italian population. J Dermatol. 1998. 25:691–694.
Article
22. Hornblass A, Stefano JA. Pigmented basal cell carcinoma of the eyelids. Am J Ophthalmol. 1981. 92:193–197.
Article
23. Farhi D, Dupin N, Palangié A, Carlotti A, Avril MF. Incomplete excision of basal cell carcinoma: rate and associated factors among 362 consecutive cases. Dermatol Surg. 2007. 33:1207–1214.
Article
24. Sexton M, Jones DB, Maloney ME. Histologic pattern analysis of basal cell carcinoma. Study of a series of 1039 consecutive neoplasms. J Am Acad Dermatol. 1990. 23:1118–1126.
Full Text Links
  • AD
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr