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Computed tomography findings of Crouzon syndrome: A case report

Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ultrasonographic assessment. Once Crouzon syndrome is susp...

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Autores principales: Neira, Juan Guillermo Arámbula, Herazo, Valeria del Castillo, Cuenca, Nury Tatiana Rincón, Sanabria Cano, Angélica M., Sarmiento, Maryi Fernanda Bermudez, Castro, María F., Ortiz, Andrés Felipe Herrera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857571/
https://www.ncbi.nlm.nih.gov/pubmed/35242254
http://dx.doi.org/10.1016/j.radcr.2022.01.060
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author Neira, Juan Guillermo Arámbula
Herazo, Valeria del Castillo
Cuenca, Nury Tatiana Rincón
Sanabria Cano, Angélica M.
Sarmiento, Maryi Fernanda Bermudez
Castro, María F.
Ortiz, Andrés Felipe Herrera
author_facet Neira, Juan Guillermo Arámbula
Herazo, Valeria del Castillo
Cuenca, Nury Tatiana Rincón
Sanabria Cano, Angélica M.
Sarmiento, Maryi Fernanda Bermudez
Castro, María F.
Ortiz, Andrés Felipe Herrera
author_sort Neira, Juan Guillermo Arámbula
collection PubMed
description Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ultrasonographic assessment. Once Crouzon syndrome is suspected, advanced imaging methods such as three-dimensional computed tomography must be requested, showing early signs of cranial sutures fusion. In this paper, we present a case of a six-year-old girl who was taken to a pediatrician control appointment due to abnormal facies. During the physical examination, a suspicion of Crouzon syndrome was raised. Therefore, a head computed tomography was requested, showing asymmetrical calvarium thickening, diffuse indentation of the inner table of the skull, and moderate hydrocephalus with a big cyst in the posterior fossa. Due to these findings, the patient was remitted to maxillofacial surgery for further evaluation; however, the medical appointment could not be achieved as a consequence of the poor medical insurance of the girl. This paper aims to describe and discuss the computed tomography findings of Crouzon syndrome.
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spelling pubmed-88575712022-03-02 Computed tomography findings of Crouzon syndrome: A case report Neira, Juan Guillermo Arámbula Herazo, Valeria del Castillo Cuenca, Nury Tatiana Rincón Sanabria Cano, Angélica M. Sarmiento, Maryi Fernanda Bermudez Castro, María F. Ortiz, Andrés Felipe Herrera Radiol Case Rep Case Report Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ultrasonographic assessment. Once Crouzon syndrome is suspected, advanced imaging methods such as three-dimensional computed tomography must be requested, showing early signs of cranial sutures fusion. In this paper, we present a case of a six-year-old girl who was taken to a pediatrician control appointment due to abnormal facies. During the physical examination, a suspicion of Crouzon syndrome was raised. Therefore, a head computed tomography was requested, showing asymmetrical calvarium thickening, diffuse indentation of the inner table of the skull, and moderate hydrocephalus with a big cyst in the posterior fossa. Due to these findings, the patient was remitted to maxillofacial surgery for further evaluation; however, the medical appointment could not be achieved as a consequence of the poor medical insurance of the girl. This paper aims to describe and discuss the computed tomography findings of Crouzon syndrome. Elsevier 2022-02-17 /pmc/articles/PMC8857571/ /pubmed/35242254 http://dx.doi.org/10.1016/j.radcr.2022.01.060 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Neira, Juan Guillermo Arámbula
Herazo, Valeria del Castillo
Cuenca, Nury Tatiana Rincón
Sanabria Cano, Angélica M.
Sarmiento, Maryi Fernanda Bermudez
Castro, María F.
Ortiz, Andrés Felipe Herrera
Computed tomography findings of Crouzon syndrome: A case report
title Computed tomography findings of Crouzon syndrome: A case report
title_full Computed tomography findings of Crouzon syndrome: A case report
title_fullStr Computed tomography findings of Crouzon syndrome: A case report
title_full_unstemmed Computed tomography findings of Crouzon syndrome: A case report
title_short Computed tomography findings of Crouzon syndrome: A case report
title_sort computed tomography findings of crouzon syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857571/
https://www.ncbi.nlm.nih.gov/pubmed/35242254
http://dx.doi.org/10.1016/j.radcr.2022.01.060
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