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Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker

A 65-year-old male presented with a 3-year history of orbital symptoms. An imaging-based diagnosis of fibrous dysplasia involving the skull base was made at another institution. CT showed a diffuse sinonasal mass and ground-glass appearance of the bones of the anterior skull base with bony defects a...

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Autores principales: Ahmed, Manzoor, Knott, Phillip Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Radiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909850/
https://www.ncbi.nlm.nih.gov/pubmed/24497807
http://dx.doi.org/10.3348/kjr.2014.15.1.156
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author Ahmed, Manzoor
Knott, Phillip Daniel
author_facet Ahmed, Manzoor
Knott, Phillip Daniel
author_sort Ahmed, Manzoor
collection PubMed
description A 65-year-old male presented with a 3-year history of orbital symptoms. An imaging-based diagnosis of fibrous dysplasia involving the skull base was made at another institution. CT showed a diffuse sinonasal mass and ground-glass appearance of the bones of the anterior skull base with bony defects and mucocele formation. MRI demonstrated an accompanying intracranial and orbital rind of soft tissue mass along the hyperostotic bones. FDG-PET showed corresponding intense hypermetabolism. Small cysts were observed at the tumor-brain interface. Biopsy revealed esthesioneuroblastoma with bone infiltration that is compatible with the hyperostotic variant of esthesioneuroblastoma. There are a few cases of hyperostotic esthesioneuroblastoma reported in the literature.
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spelling pubmed-39098502014-02-04 Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker Ahmed, Manzoor Knott, Phillip Daniel Korean J Radiol Neuroimaging and Head and Neck A 65-year-old male presented with a 3-year history of orbital symptoms. An imaging-based diagnosis of fibrous dysplasia involving the skull base was made at another institution. CT showed a diffuse sinonasal mass and ground-glass appearance of the bones of the anterior skull base with bony defects and mucocele formation. MRI demonstrated an accompanying intracranial and orbital rind of soft tissue mass along the hyperostotic bones. FDG-PET showed corresponding intense hypermetabolism. Small cysts were observed at the tumor-brain interface. Biopsy revealed esthesioneuroblastoma with bone infiltration that is compatible with the hyperostotic variant of esthesioneuroblastoma. There are a few cases of hyperostotic esthesioneuroblastoma reported in the literature. The Korean Society of Radiology 2014 2014-01-08 /pmc/articles/PMC3909850/ /pubmed/24497807 http://dx.doi.org/10.3348/kjr.2014.15.1.156 Text en Copyright © 2014 The Korean Society of Radiology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Neuroimaging and Head and Neck
Ahmed, Manzoor
Knott, Phillip Daniel
Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker
title Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker
title_full Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker
title_fullStr Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker
title_full_unstemmed Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker
title_short Hyperostotic Esthesioneuroblastoma: Rare Variant and Fibrous Dysplasia Mimicker
title_sort hyperostotic esthesioneuroblastoma: rare variant and fibrous dysplasia mimicker
topic Neuroimaging and Head and Neck
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909850/
https://www.ncbi.nlm.nih.gov/pubmed/24497807
http://dx.doi.org/10.3348/kjr.2014.15.1.156
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