Literature DB >> 10332131

Early diagnosis of nevoid basal cell carcinoma syndrome.

L Lo Muzio1, P Nocini, P Bucci, G Pannone, U Consolo, M Procaccini.   

Abstract

BACKGROUND: Nevoid basal cell carcinoma syndrome, or NBCCS, is a hereditary condition characterized by basal cell carcinomas, or BCCs; odontogenic keratocysts, or OKCs; and skeletal abnormalities. The authors conducted this study to determine the early signs of NBCCS.
METHODS: The authors reviewed files from two Italian dental schools from January 1980 to January 1995 to determine the early signs of NBCCS and the age at which patients were first examined. They re-examined all of the patients, using the diagnostic criteria for NBCCS.
RESULTS: The authors found 14 patients who fulfilled the criteria for diagnosis of NBCCS in five families. All of the patients were 16 years of age or younger. In 11 cases (78 percent), the first sign of NBCCS in the patients was an OKC. The OKCs diagnosed in patients older than 13 years of age were large and characterized by widespread bone resorption. One 11-year-old patient had six large OKCs. The authors also found a case of multiple OKCs in an 8-year-old patient. Only one patient showed BCCs.
CONCLUSIONS: OKCs are often the first signs of NBCCS and can be detected in patients younger than 10 years of age. Our data suggest that OKCs arise earlier in patients who have NBCCS than in patients who do not have NBCCS. The patients' young ages explain the low incidence of BCCs in this study. CLINICAL IMPLICATIONS: The presence of multiple OKCs in a child or onset of BCC in a patient younger than 20 years of age should alert dentists to the possibility of the patient's having NBCCS.

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Year:  1999        PMID: 10332131     DOI: 10.14219/jada.archive.1999.0276

Source DB:  PubMed          Journal:  J Am Dent Assoc        ISSN: 0002-8177            Impact factor:   3.634


  25 in total

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2.  Clinical utility gene card for: Gorlin syndrome.

Authors:  Lorenzo Lo Muzio; Lorenza Pastorino; Sonja Levanat; Vesna Musani; Mima Situm; Giovanna Bianchi Scarra
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3.  Clinical utility gene card for: Gorlin syndrome--update 2013.

Authors:  Lorenzo Lo Muzio; Lorenza Pastorino; Sonja Levanat; Vesna Musani; Mima Situm; Giovanni Ponti; Giovanna Bianchi Scarra
Journal:  Eur J Hum Genet       Date:  2013-01-30       Impact factor: 4.246

4.  Multiple non-syndromic odontogenic keratocysts in three siblings.

Authors:  Amit Nirwan; Sangeeta Panjab Wanjari; Rashmi Saikhedkar; Vinayak Karun
Journal:  BMJ Case Rep       Date:  2013-03-14

5.  Radiological features of familial Gorlin-Goltz syndrome.

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6.  Two Cases of Nevoid Basal Cell CarcinomaSyndrome in One Family.

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Review 7.  [Identification of rare diseases in the oral cavity].

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Review 9.  Nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Authors:  Lorenzo Lo Muzio
Journal:  Orphanet J Rare Dis       Date:  2008-11-25       Impact factor: 4.123

10.  Neuroimaging of nevoid basal cell carcinoma syndrome (NBCCS) in children.

Authors:  Kamyar Sartip; Adam Kaplan; George Obeid; Nadja Kadom
Journal:  Pediatr Radiol       Date:  2012-11-14
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