METASTATIC BASAL-CELL CARCINOMA - REPORT OF 5 CASES

Citation
Sn. Snow et al., METASTATIC BASAL-CELL CARCINOMA - REPORT OF 5 CASES, Cancer, 73(2), 1994, pp. 328-335
Citations number
61
Categorie Soggetti
Oncology
Journal title
CancerACNP
ISSN journal
0008543X
Volume
73
Issue
2
Year of publication
1994
Pages
328 - 335
Database
ISI
SICI code
0008-543X(1994)73:2<328:MBC-RO>2.0.ZU;2-L
Abstract
Background. Metastatic basal cell carcinoma (MBCC) is rare. Risk facto rs for the development of MBCC include a history of persistent basal c ell carcinoma (BCC) for many years, refractory to conventional methods of treatment and previous radiation treatment either in early adultho od or for localized cancer. Most MBCC originate from large tumors. Met hods. The authors report five patients with basal cell carcinomas (BCC ) of the ear (two patients), scalp, inner canthus, and nasolabial fold that metastasized to the regional lymph nodes, skin, and submandibula r gland. In addition, the authors reviewed more than 40 reports of MBC C (n = 65) from 1981 to 1991 and tabulated the primary tumors by size and depth of invasion according to TNM classification, a classificatio n that previously has not been used for BCC. Results. The authors tabu lated the size distribution of tumors of 45 patients with MBCC. The ov erall mean and median diameters of the primary BCC were 8.7 and 7.0 cm , respectively. The mean area of the primary MBCC lesion that originat ed on the face and trunk was 62 and 217 cm(2), respectively. Using the TNM classification, approximately 9% of MBCC originate from tumors sm aller than 10 cm(2). In addition, the authors found that large (T2 and T3) and deep (T4) BCC account for approximately 75% of the metastatic tumors. Metastatic ECC from primary tumors smaller than 1 cm in diame ter are exceptionally rare. Conclusions. Approximately 67% of MBCC (n = 238) originate from facial sites. Using the data base of the Mohs Su rgery Clinic, the authors found that BCC greater than 3 cm in diameter have approximately a 1.9% incidence of metastasis, and the overall ra te of metastases for morpheaform BCC is less than 1%. Patients with tu mors classified as T3 and T4 lesions ideally should be followed up for 10 or more years for the remote possibility of the development of MBC C.