Nevoid Basal-Cell Syndrome: literature review and case report in a family

Author:

Tincani Alfio José1,Martins Antônio Santos1,Andrade Ricardo Gomes1,Mello Jr. Edgar José Franco1,Bueno Marco Antônio Camargo1

Affiliation:

1. UNICAMP, Brazil

Abstract

The Nevoid Basal-Cell Carcinoma Syndrome (NBCC), or as it is also referred to, basal-cell nevus syndrome or Gorlin-Goltz syndrome, is characterized by multiple early-appearing basal cell carcinomas, keratocytosis of the mandible, and anomalies of the ocular, skeletal reproductive system. We describe four patients in the same family, all of them possessing a large number of skin tumors associated with other typical clinical and X-Ray anomalies of NBCC. The definitive treatment of NBCC has yet to be established, however, early diagnosis is very important as well as the periodical follow-up examination of ten patients, mainly due to the transformations in the skin lesions that may occur.

Publisher

FapUNIFESP (SciELO)

Subject

General Medicine

Reference19 articles.

1. The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma;Evans D.G.R.;Br J Cancer,1991

2. Location of gene for Gorlin syndrome;Famdon RA.;Lancet,1992

3. Studies on the genetics of basal cell nevus syndrome in one family;Gao J.;Chin Med J,1985

4. Multiple novoid basal-cell epithelioma jaw cysts and bifid rib;Gorlin R.J.;N Eng J Med,1960

5. Nevoid basal-cell carcinoma syndrome;Gorlin R.J.;Medicine,1987

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