Results 71 to 80 of about 1,227,254 (171)

Delayed Pulmonary Metastasis of Basal Cell Carcinoma 10 Years After Primary Excision: A Case Report and Literature Review

Case Reports in Medicine, Volume 2025, Issue 1, 2025.
Background: Basal cell carcinoma (BCC) is the most common cutaneous malignancy, characterized by slow progression and a low propensity for metastasis. Metastatic basal cell carcinoma (mBCC) occurs in fewer than 0.1% of the cases, most frequently involving the lungs, lymph nodes, or bones.
Hazhir Moradi, Negar Karavan, Forough Kalantari, Elham Kalantari, Viswanatha Borlingegowda   +4 more
wiley   +1 more source

Nevoid basal cell carcinoma syndrome (Gorlin syndrome): a case report

Journal of Medical Case Reports
Background Basal cell nevus syndrome, also known as Gorlin or Gorlin–Goltz syndrome, is a hereditary condition caused by mutation in the PATCHED gene.
Noura Abdul Rahman, Fatima Breim, Joud Zakour, Zainab Srouji, Silva Ishkhanian   +4 more
doaj   +1 more source

Gorlin-Goltz Syndrome: Case Report of a Rare Hereditary Disorder

Case Reports in Dentistry, 2012
Introduction. Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. Case Report.
Ashutosh Agrawal, Aditi Murari, Sunil Vutukuri, Arun Singh   +3 more
doaj   +1 more source

Basal Cell Nevus Syndrome Treated With Laser Therapy: Novel Approach for Young Adults

International Journal of Dermatology, Volume 65, Issue 2, Page 362-364, February 2026.
Giulia Briatico, Camila Scharf, Eugenia Veronica Di Brizzi, Gabriella Brancaccio, Nikola Drmac   +4 more
wiley   +1 more source

Clinicopathological and molecular spectrum of patients with germline SUFU mutations: A case series

Journal of Cutaneous Pathology, Volume 51, Issue 12, Page 980-986, December 2024.
Abstract Background One of the hereditary syndromes associated with multiple early‐onset basal cell carcinomas (BCCs) is basal cell nevus syndrome (BCNS), of which a minority is caused by germline SUFU mutations. Germline SUFU mutations show a spectrum of phenotypes, of which multiple hereditary infundibulocystic basal cell carcinoma syndrome (MHIBCC ...
Mashiro van Dal, Sanne R. Martens‐de Kemp, Antien L. Mooyaart, Walter Voogt, Marlies Wakkee, Jeffrey Damman   +5 more
wiley   +1 more source

Phenotypes, Genetics, and Estimated Prevalence of Focal Dermal Hypoplasia (Goltz Syndrome): A Single‐Center Report

Pediatric Dermatology, Volume 41, Issue 6, Page 1106-1113, November/December 2024.
ABSTRACT Background Focal dermal hypoplasia (FDH), also known as Goltz syndrome, is a rare ectodermal dysplasia that primarily affects the skin, skeleton, and eyes. It is an X‐linked dominant disorder, predominantly seen in females, caused by pathogenic variants in PORCN. Methods We characterized a case series of four genetically confirmed FDH patients
Laura Krogh Herlin, Morten Krogh Herlin, Hanne Vinter, Jenny Blechingberg, Brian Nauheimer Andersen, Casper Kruse, Mette Sommerlund   +6 more
wiley   +1 more source

Gorlin-Goltz: what's in a name?

, 1998
This paper describes the clinical features of two very distinct syndromes with similar names: Gorlin-Goltz and Goltz-Gorlin Syndromes. A case report is presented that highlights the differences between these syndromes.
Trotman, C A, Russell, K A, McNamara, T
core  

Analysis of basal cell carcinomas' histological subtypes and relative response to vismodegib in six patients diagnosed with Gorlin–Goltz syndrome: A retrospective study

, 2023
Analysis of basal cell carcinomas' histological subtypes and relative response to vismodegib in six patients diagnosed with Gorlin–Goltz syndrome: A retrospective ...
Melotti B., Comito F., Baraldi C., Dika E., Venturi F., Lambertini M., Scotti B.   +6 more
core   +1 more source

[Gorlin-Goltz syndrome].

Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University, 1991
Gorlin-Goltz syndrome has mainly three components; basal cell carcinoma, jaw cysts and skeletal anomalies. However, various cases of this syndrome with over 40 different kinds of components have been reported. In this paper, a case with Gorlin-Goltz syndrome treated in our clinic have been presented and discussed.
K, Sevin, N, Kutlu, M O, Yenidünya
openaire   +3 more sources

Gorlin-Goltz syndrome

Journal of Dr. NTR University of Health Sciences, 2013
Gorlin-Goltz syndrome is an inherited autosomal dominant disorder characterized by the presence of multiple odontogenic keratocysts of jaws, basal cell carcinomas, palmar, plantar pits and intracranial calcifications. Apart from these many dental, skeletal, ophthalmic and neurological abnormalities have been reported.
Shyam N. Sunder, Suresh Babburi, Srikanth Guduguntla, P. S. Raju   +3 more
openaire   +1 more source