Literature DB >> 25838663

Nevoid Basal cell carcinoma syndrome: a case report and review.

S Bala Subramanyam1, D Naga Sujata1, K Sridhar2, M Pushpanjali1.   

Abstract

Nevoid basal cell carcinoma syndrome, a rare autosomal dominant disorder, comprises of a number of abnormalities such as multiple nevoid basal cell carcinomas, skeletal abnormalities and multiple keratocystic odontogenic tumors. Diagnosis may be difficult because of the variability of expressivity and different ages of onset for different traits of this disorder. The dental clinician may be the first to encounter and identify this syndrome, when the multiple cysts like radiolucencies are discovered on panoramic view. This article reports a case of Nevoid basal cell carcinoma syndrome and provides an overview on diagnosis and management.

Entities:  

Keywords:  Goltz syndrome; Gorlin; Keratocystic odontogenic tumor; NBCCS

Year:  2011        PMID: 25838663      PMCID: PMC4379239          DOI: 10.1007/s12663-011-0262-5

Source DB:  PubMed          Journal:  J Maxillofac Oral Surg        ISSN: 0972-8270


  14 in total

1.  Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome.

Authors:  R J GORLIN; R W GOLTZ
Journal:  N Engl J Med       Date:  1960-05-05       Impact factor: 91.245

2.  Excision of the overlying, attached mucosa, in conjunction with cyst enucleation and treatment of the bony defect with carnoy solution.

Authors:  Paul J W Stoelinga
Journal:  Oral Maxillofac Surg Clin North Am       Date:  2003-08       Impact factor: 2.802

3.  Prenatal diagnosis of Gorlin syndrome.

Authors:  M G Bialer; M R Gailani; J A McLaughlin; B Petrikovsky; A E Bale
Journal:  Lancet       Date:  1994-08-13       Impact factor: 79.321

Review 4.  Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome.

Authors:  V E Kimonis; A M Goldstein; B Pastakia; M L Yang; R Kase; J J DiGiovanna; A E Bale; S J Bale
Journal:  Am J Med Genet       Date:  1997-03-31

5.  Nevoid basal cell carcinoma syndrome. Clinical findings in 37 Italian affected individuals.

Authors:  L Lo Muzio; P F Nocini; A Savoia; U Consolo; M Procaccini; L Zelante; G Pannone; P Bucci; M Dolci; F Bambini; P Solda; G Favia
Journal:  Clin Genet       Date:  1999-01       Impact factor: 4.438

6.  Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site.

Authors:  J W Bare; R V Lebo; E H Epstein
Journal:  Cancer Res       Date:  1992-03-15       Impact factor: 12.701

7.  Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.

Authors:  D G Evans; E J Ladusans; S Rimmer; L D Burnell; N Thakker; P A Farndon
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

8.  Brain tumours and the occurrence of severe invasive basal cell carcinoma in first degree relatives with Gorlin syndrome.

Authors:  D G Evans; J M Birch; C I Orton
Journal:  Br J Neurosurg       Date:  1991       Impact factor: 1.596

9.  Nevoid basal cell carcinoma syndrome. A 15-year follow-up of cases in Ottawa and the Ottawa Valley.

Authors:  M D Pratt; R Jackson
Journal:  J Am Acad Dermatol       Date:  1987-05       Impact factor: 11.527

10.  Location of gene for Gorlin syndrome.

Authors:  P A Farndon; R G Del Mastro; D G Evans; M W Kilpatrick
Journal:  Lancet       Date:  1992-03-07       Impact factor: 79.321

View more
  2 in total

1.  A multidisciplinary approach to the successful management of Gorlin syndrome.

Authors:  Ryan N Mello; Zaki Khan; Umar Choudry
Journal:  J Surg Case Rep       Date:  2017-06-08

Review 2.  Imaging More than Skin-Deep: Radiologic and Dermatologic Presentations of Systemic Disorders.

Authors:  Mehrzad Shafiei; Firoozeh Shomal Zadeh; Bahar Mansoori; Hunter Pyle; Nnenna Agim; Jorge Hinojosa; Arturo Dominguez; Cristina Thomas; Majid Chalian
Journal:  Diagnostics (Basel)       Date:  2022-08-19
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.