Cargando…

Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones

Spontaneous tegmen tympani defects are rare with even rarer bilateral cases. The symptoms are nonspecific; hence, a high index of suspicion is required to prevent serious intracranial complications. We present a case of spontaneous bilateral tegmen tympani defects with associated meningoencephalocoe...

Descripción completa

Detalles Bibliográficos
Autores principales: Rose, Oliver, Neeff, Michel, Low, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830780/
https://www.ncbi.nlm.nih.gov/pubmed/24288640
http://dx.doi.org/10.1155/2013/969762
_version_ 1782291520887455744
author Rose, Oliver
Neeff, Michel
Low, Christopher
author_facet Rose, Oliver
Neeff, Michel
Low, Christopher
author_sort Rose, Oliver
collection PubMed
description Spontaneous tegmen tympani defects are rare with even rarer bilateral cases. The symptoms are nonspecific; hence, a high index of suspicion is required to prevent serious intracranial complications. We present a case of spontaneous bilateral tegmen tympani defects with associated meningoencephalocoeles in a 54-year-old male who presented with the signs and symptoms of severe meningitis. After careful workup which included a lumbar puncture, CT and MRI scans, both defects were repaired using a middle fossa approach. The patient made an uneventful recovery with complete cessation of otorrhoea and improvement in his hearing.
format Online
Article
Text
id pubmed-3830780
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-38307802013-11-28 Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones Rose, Oliver Neeff, Michel Low, Christopher Case Rep Otolaryngol Case Report Spontaneous tegmen tympani defects are rare with even rarer bilateral cases. The symptoms are nonspecific; hence, a high index of suspicion is required to prevent serious intracranial complications. We present a case of spontaneous bilateral tegmen tympani defects with associated meningoencephalocoeles in a 54-year-old male who presented with the signs and symptoms of severe meningitis. After careful workup which included a lumbar puncture, CT and MRI scans, both defects were repaired using a middle fossa approach. The patient made an uneventful recovery with complete cessation of otorrhoea and improvement in his hearing. Hindawi Publishing Corporation 2013 2013-10-29 /pmc/articles/PMC3830780/ /pubmed/24288640 http://dx.doi.org/10.1155/2013/969762 Text en Copyright © 2013 Oliver Rose et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rose, Oliver
Neeff, Michel
Low, Christopher
Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones
title Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones
title_full Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones
title_fullStr Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones
title_full_unstemmed Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones
title_short Spontaneous Bilateral Meningoencephalocoeles of the Temporal Bones
title_sort spontaneous bilateral meningoencephalocoeles of the temporal bones
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830780/
https://www.ncbi.nlm.nih.gov/pubmed/24288640
http://dx.doi.org/10.1155/2013/969762
work_keys_str_mv AT roseoliver spontaneousbilateralmeningoencephalocoelesofthetemporalbones
AT neeffmichel spontaneousbilateralmeningoencephalocoelesofthetemporalbones
AT lowchristopher spontaneousbilateralmeningoencephalocoelesofthetemporalbones