Fini, Giuseppina and Belli, E. and Mici, Elidon and Virciglio, Pasquale and Moricca, Luca Maria and D'Itri, L. and Leonardi, A. and Malavenda, M.S. and Krizzuk, D. and Merola, R. and Maturo, A. and Pasta, Vittorio (2013) Nevoid basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Case report. Il giornale di chirurgia, 34 (5/6). pp. 176-179. ISSN 1971-145X
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Abstract
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome (NBCCS) comprises multiple basal cell carcinomas, keratocysts of the jaw, palmar/plantar pits, spine and rib anomalies, calcifications of the falx cerebri etc. The diagnosis is made according to clinical criteria (Kimonis Criteria) and genetic ones. We studied one family where father and then his sun resulted affected by each syndrome. Gorlin-Goltz syndrome is a rare disease diagnosed according to clinical criteria sometimes difficult to integrate. The family case we presented shows how you can get diagnosis even in older age and after numerous surgeries. Patients should be given special attention and therefore should be monitorized and need multidisciplinary treatments continued in time, even a trivial change of signs and symptoms may be an important indicator of a precipitating event which puts the patient's life under threat.
Item Type: | Article |
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Uncontrolled Keywords: | Nevoid basal cell carcinoma syndrome,Gorlin-Goltz Syndrome Basal cell carcinoma - Mandibular keratocysts - Surgery |
Subjects: | 600 Tecnologia - Scienze applicate > 610 Medicina e salute (Classificare qui la tecnologia dei servizi medici) > 617 Rami vari della medicina; Chirurgia |
Depositing User: | Nadia Del Gobbo |
Date Deposited: | 12 Sep 2019 12:34 |
Last Modified: | 12 Sep 2019 12:34 |
URI: | http://eprints.bice.rm.cnr.it/id/eprint/8438 |
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