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Rare osteodysplasia of the temporal bone

Temporal bone osteodysplasia can produce many different symptoms, such as involvement restricted to the temporal bone or impairment of other bones. We consider, in this study two entities that are rare osteodysplasia cases, which are osteopetrosis and Camurati-Engelmann disease, the latter being ext...

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Autores principales: Antunes, Marcos L., Testa, José R.G., Frazatto, Ricardo, Barberi, José A.F., Silva, Rogério F.N.D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450549/
https://www.ncbi.nlm.nih.gov/pubmed/16446922
http://dx.doi.org/10.1016/S1808-8694(15)31315-X
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author Antunes, Marcos L.
Testa, José R.G.
Frazatto, Ricardo
Barberi, José A.F.
Silva, Rogério F.N.D.
author_facet Antunes, Marcos L.
Testa, José R.G.
Frazatto, Ricardo
Barberi, José A.F.
Silva, Rogério F.N.D.
author_sort Antunes, Marcos L.
collection PubMed
description Temporal bone osteodysplasia can produce many different symptoms, such as involvement restricted to the temporal bone or impairment of other bones. We consider, in this study two entities that are rare osteodysplasia cases, which are osteopetrosis and Camurati-Engelmann disease, the latter being extremely rare. We present two cases of benign form of osteopetrosis (Albers-Schulenburg's disease), a patient of 11 years old and another one of 48 years old, both male, and a patient of 28 years old, female, with Camurati-Engelmann's disease. The facial palsy was a manifestation in two of the patients. We discuss some aspects about the clinical manifestations, radiological findings, as well as differential diagnostic and therapy in view of the complications of the diseases.
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spelling pubmed-94505492022-09-09 Rare osteodysplasia of the temporal bone Antunes, Marcos L. Testa, José R.G. Frazatto, Ricardo Barberi, José A.F. Silva, Rogério F.N.D. Braz J Otorhinolaryngol Case Report Temporal bone osteodysplasia can produce many different symptoms, such as involvement restricted to the temporal bone or impairment of other bones. We consider, in this study two entities that are rare osteodysplasia cases, which are osteopetrosis and Camurati-Engelmann disease, the latter being extremely rare. We present two cases of benign form of osteopetrosis (Albers-Schulenburg's disease), a patient of 11 years old and another one of 48 years old, both male, and a patient of 28 years old, female, with Camurati-Engelmann's disease. The facial palsy was a manifestation in two of the patients. We discuss some aspects about the clinical manifestations, radiological findings, as well as differential diagnostic and therapy in view of the complications of the diseases. Elsevier 2015-10-20 /pmc/articles/PMC9450549/ /pubmed/16446922 http://dx.doi.org/10.1016/S1808-8694(15)31315-X Text en . https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Antunes, Marcos L.
Testa, José R.G.
Frazatto, Ricardo
Barberi, José A.F.
Silva, Rogério F.N.D.
Rare osteodysplasia of the temporal bone
title Rare osteodysplasia of the temporal bone
title_full Rare osteodysplasia of the temporal bone
title_fullStr Rare osteodysplasia of the temporal bone
title_full_unstemmed Rare osteodysplasia of the temporal bone
title_short Rare osteodysplasia of the temporal bone
title_sort rare osteodysplasia of the temporal bone
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450549/
https://www.ncbi.nlm.nih.gov/pubmed/16446922
http://dx.doi.org/10.1016/S1808-8694(15)31315-X
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