Results 81 to 90 of about 6,707,637 (199)

Gorlin syndrome: Importance of clinical signs and danger of delayed diagnosis - A case report with eight years follow-up

open access: yesArchives of Clinical and Experimental Surgery, 2015
Nevoid basal cell carcinoma (NBCCS) or Gorlin-Goltz syndrome (GS) is a multidisciplinary problem, the early diagnosis of which allows secondary prophylaxis that follows an appropriate regimen to delay progression of the syndrome.
Erica Dorigatti de-Avila   +4 more
doaj   +1 more source

Ultrapulse CO2 Used for the Successful Treatment of Basal Cell Carcinomas Found in Patients with Basal Cell Nevus Syndrome

open access: yes, 2002
background. Basal cell nevus syndrome (BCNS) is an inherited condition marked by multiple basal cell carcinomas (BCCs) associated with several other abnormalities. Various treatment modalities have been used to eradicate these tumors.
Trent, Jennifer T   +3 more
core   +1 more source

A case of skin lesions of basal cell nevus syndrome. [PDF]

open access: yesPostepy Dermatol Alergol, 2021
Chen L, Sun H, Zuo M, Xi Q.
europepmc   +1 more source

Risk of basal cell carcinoma after Hodgkin's disease [PDF]

open access: yes, 2000
Background: Basal cell cancer is a common skin cancer, yet studies of second tumors after Hodgkin's disease tend to exclude basal cell cancers as second malignant tumors from analysis.
Hölzel, Dieter   +5 more
core   +1 more source

The Gorlin-Goltz syndrome: a sporadic case

open access: yesThe Pan African Medical Journal, 2014
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant hereditary disorder; which is characterized by numerous basal cell carcinomas, maxillary keratocysts and bones malformations.
Kawtar Inani, Fatimazahra Mernissi
doaj   +1 more source

Nevoid basal cell carcinoma syndrome: A case report

open access: yesJournal of Dr. NTR University of Health Sciences, 2018
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in patch (PTCH), a tumor suppressor gene that has been mapped to ...
Venkatesh K Dodda   +3 more
doaj   +1 more source

Characterization of intractable diarrhea resulting from vismodegib treatment for basal cell nevus syndrome. [PDF]

open access: yesJAAD Case Rep, 2023
Patel A   +6 more
europepmc   +1 more source

Trichilemmal cyst nevus with a sebaceous nevus component [PDF]

open access: yes, 2010
A 23-year-old man with a typical trichilemmal cyst nevus is reported. This recently described disorder is sufficiently characteristic to differentiate it from sebaceous nevus, nevus comedonicus, porokeratotic eccrine nevus, nevus corniculatus, follicular
Haneke, Eckart   +8 more
core   +2 more sources

Fibrothecoma of Ovary [PDF]

open access: yesPerspectives In Medical Research, 2017
Ovarian fibrothecomas represent an ovarian stromal neoplasm developing in a wide spectrum of clinical settings. Fibrothecomas have been described as rare neoplasms.
B Pratyusha1 , Anandam G2 , Sharadrutha3
doaj  

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