Basal Cell Nevus Syndrome Showing Several Histologic Types of Basal Cell Carcinoma
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Basal Cell Nevus Syndrome Showing Several Histologic Types of Basal Cell Carcinoma
Basal cell nevus syndrome (BCNS), or Gorlin Syndrome, is an autosomal dominant disorder, characterized by multiple developmental abnormalities and associated with germline mutations in the PTCH gene. Patients show multiple and early onset basal cell carcinomas (BCCs) in skin, odontogeniccysts in the jaw, pits on palms and soles, medulloblastoma, hypertelorism, and calcification of the falx cere...
متن کاملRetraction: Basal Cell Nevus Syndrome Showing Several Histologic Types of Basal Cell Carcinoma
On September 30, 2011, Annals of Dermatology in Volume 23, Number Supplementary 1, published a case report by Go JW, et al. on the basal cell nevus syndrome. We accepted the article after having been informed in writing, by the authors, that it had not been submitted for publication elsewhere. In fact, however, the same case had already been reported by Moon MS, et al., the colleagues in the sa...
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Background: Basal cell carcinoma (BCC), the most common form of skin cancer, usually occurs in the sun-exposed areas of the body like head and neck, yet is also seen in unexpected sites. Myriad studies have mentioned a lower limb BCC incidence rate of 1.5-13.5%.Methods: The present retrospective cross-sectional study was conducted on 650 BCC patients, who were referred to the dermatology tumor ...
متن کاملnaevoid basal cell carcinoma syndrome
nevoid basal cell carcinoma syndrome (nbccs), also known as gorlin syndrome, is a hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms . the estimated prevalence varies from 1/57,000 to 1/256,000, with a male-to-female ratio of 1:1. main clinical manifestations include multiple basal cell carcinomas (bccs), odontogenic keratocysts o...
متن کامل[A case of basal cell nevus syndrome].
A case of basal cell nevus syndrome is reported. The patient, a 25-year-old man, had no family history of this condition. The patient showed multiple mandibular cysts, calcification of the falx cerebri, bridging of the sella turcica, ocular hypertelorimsm, a broad nasal root, and pitting of the palms. These findings correlate with reports in the literature and permitted the diagnosis of basal c...
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ژورنال
عنوان ژورنال: Annals of Dermatology
سال: 2011
ISSN: 1013-9087
DOI: 10.5021/ad.2011.23.s1.s36