Results 61 to 70 of about 1,573 (165)
A malignant transformation is known to occur in many nevi such as a sebaceous nevus or a basal cell nevus, but a verrucous epidermal nevus has only rarely been associated with neoplastic changes.
Hassan Riad +5 more
doaj +1 more source
Neglected Fungating Giant basal cell carcinoma: A case report and literature review
Key Clinical Message Gaint fungating BCC is rare and aggressive. Early health‐seeking behavior may result in positive outcomes. Abstract Fungating giant basal cell carcinoma (BCC) is a rare and aggressive form of BCC infrequently reported in the literature. We present a giant BCC case in an old female from a rural area with a poor socioeconomic profile.
Susmin Karki +7 more
wiley +1 more source
Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms.
Ellen Toyonaga +5 more
doaj +1 more source
There was no association between PTCH1 genetic variants (rs357564, rs2236405, rs2297086, and rs41313327) and BCC development in the Western Mexico population. PTCH1 mRNA and protein were underexpressed in BCC patients. Abstract Background Basal cell carcinoma (BCC) represents about 80% of all cases of skin cancer.
Marianela Zambrano‐Román +6 more
wiley +1 more source
Nevoid Basal-Cell Syndrome: literature review and case report in a family
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 ...
Alfio José Tincani +4 more
doaj +1 more source
Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent multisystemic disease inherited in a dominant autosomal way, which shows a high level of penetrance and variable expressiveness.
B V Shobha +5 more
doaj +1 more source
A Rare Case of Gorlin-Goltz Syndrome in Children
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an autosomal dominant condition disorder with high variability expression.
Fernanda Brasil Daura Jorge Boos Lima +6 more
doaj +1 more source
Gorlin syndrome - an incidental radiographic detection
Gorlin-Goltz syndrome (also known as nevoid basal cell carcinoma syndrome) was first reported in 1894, but described by Gorlin and Goltz in 1960 as a distinct entity consisting of ectodermal and mesodermal abnormalities.
Shishir Ram Shetty +5 more
doaj +1 more source
Nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin Syndrome, is an autosomal dominant multisystem disorder, characterized by multiple developmental abnormalities and inactivation germline mutations in the human homolog of the patched (PTCH) gene. We
S. AlSalem, Y. Binamer
doaj +1 more source
Non-syndromic multiple keratocyst odontogenic tumor: A rare case report
Keratocystic odontogenic tumors (KCOTs) are one of the most frequent features of nevoid basal cell carcinoma syndrome (NBCCS). The condition is linked with mutation in the PTCH gene.
Abhijeet Alok +3 more
doaj +1 more source

