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Fibrous dysplasia of the cranial bones: a case report and review of the literature.

Fibrous dysplasia (FD) is a relatively uncommon disorder that affects primarily the cranial region; its occurrence in the cranial base in combination with hindbrain herniation and aneurysmal bone cyst (ABC) constitutes an extremely rare condition. We report a case of polyostotic fibrous dysplasia wi...

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Detalles Bibliográficos
Autores principales: Iseri, Pervin K., Efendi, Husnu, Demirci, Ali, Komsuoglu, Sezer
Formato: Texto
Lenguaje:English
Publicado: Yale Journal of Biology and Medicine 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2259144/
https://www.ncbi.nlm.nih.gov/pubmed/16464312
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author Iseri, Pervin K.
Efendi, Husnu
Demirci, Ali
Komsuoglu, Sezer
author_facet Iseri, Pervin K.
Efendi, Husnu
Demirci, Ali
Komsuoglu, Sezer
author_sort Iseri, Pervin K.
collection PubMed
description Fibrous dysplasia (FD) is a relatively uncommon disorder that affects primarily the cranial region; its occurrence in the cranial base in combination with hindbrain herniation and aneurysmal bone cyst (ABC) constitutes an extremely rare condition. We report a case of polyostotic fibrous dysplasia with progressive occipital, temporal, and clival involvement. Clinical findings and differential diagnosis with special emphasis on the imaging features were discussed. A small posterior fossa volume has been thought to lead to hind brain herniation. The resultant obstruction to the CSF pathways at the level of the foramen magnum has been implicated in the development and subsequent progression of syringobulbia.
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spelling pubmed-22591442008-03-03 Fibrous dysplasia of the cranial bones: a case report and review of the literature. Iseri, Pervin K. Efendi, Husnu Demirci, Ali Komsuoglu, Sezer Yale J Biol Med Research Article Fibrous dysplasia (FD) is a relatively uncommon disorder that affects primarily the cranial region; its occurrence in the cranial base in combination with hindbrain herniation and aneurysmal bone cyst (ABC) constitutes an extremely rare condition. We report a case of polyostotic fibrous dysplasia with progressive occipital, temporal, and clival involvement. Clinical findings and differential diagnosis with special emphasis on the imaging features were discussed. A small posterior fossa volume has been thought to lead to hind brain herniation. The resultant obstruction to the CSF pathways at the level of the foramen magnum has been implicated in the development and subsequent progression of syringobulbia. Yale Journal of Biology and Medicine 2005-05 /pmc/articles/PMC2259144/ /pubmed/16464312 Text en
spellingShingle Research Article
Iseri, Pervin K.
Efendi, Husnu
Demirci, Ali
Komsuoglu, Sezer
Fibrous dysplasia of the cranial bones: a case report and review of the literature.
title Fibrous dysplasia of the cranial bones: a case report and review of the literature.
title_full Fibrous dysplasia of the cranial bones: a case report and review of the literature.
title_fullStr Fibrous dysplasia of the cranial bones: a case report and review of the literature.
title_full_unstemmed Fibrous dysplasia of the cranial bones: a case report and review of the literature.
title_short Fibrous dysplasia of the cranial bones: a case report and review of the literature.
title_sort fibrous dysplasia of the cranial bones: a case report and review of the literature.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2259144/
https://www.ncbi.nlm.nih.gov/pubmed/16464312
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