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A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction

Skull base osteomyelitis is classically documented as an extension of malignant otitis externa. Initial presentation commonly includes aural symptoms and cranial nerve dysfunctions. Here we present a case that emerged with multiple infarctions in the right cerebrum. A male in his 70s with diabetes m...

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Autores principales: Miyabe, Haruka, Uno, Atsuhiko, Nakajima, Takahiro, Morizane, Natsue, Enomoto, Keisuke, Hirose, Masayuki, Hazama, Toshinori, Takenaka, Yukinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997026/
https://www.ncbi.nlm.nih.gov/pubmed/27597916
http://dx.doi.org/10.1155/2016/9252361
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author Miyabe, Haruka
Uno, Atsuhiko
Nakajima, Takahiro
Morizane, Natsue
Enomoto, Keisuke
Hirose, Masayuki
Hazama, Toshinori
Takenaka, Yukinori
author_facet Miyabe, Haruka
Uno, Atsuhiko
Nakajima, Takahiro
Morizane, Natsue
Enomoto, Keisuke
Hirose, Masayuki
Hazama, Toshinori
Takenaka, Yukinori
author_sort Miyabe, Haruka
collection PubMed
description Skull base osteomyelitis is classically documented as an extension of malignant otitis externa. Initial presentation commonly includes aural symptoms and cranial nerve dysfunctions. Here we present a case that emerged with multiple infarctions in the right cerebrum. A male in his 70s with diabetes mellitus and chronic renal failure presented with left hemiparesis. Imaging studies showed that blood flow in the carotid artery remained at the day of onset but was totally occluded 7 days later. However, collateral blood supply prevented severe infarction. These findings suggest that artery-to-artery embolization from the petrous and/or cavernous portion of the carotid artery caused the multiple infarctions observed on initial presentation. Osteomyelitis of the central skull base was diagnosed on the basis of the following findings taken together: laboratory results showing high levels of inflammation, presence of Pseudomonas aeruginosa in the otorrhea and blood culture, multiple cranial nerve palsies that appeared later, the bony erosion observed on CT, and the mass lesion on MRI. Osteomyelitis was treated successfully by long-term antibiotic therapy; however, the patient experienced cefepime-induced neurotoxicity during therapy. The potential involvement of the internal carotid artery in this rare and life-threatening disease is of particular interest in this case.
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spelling pubmed-49970262016-09-05 A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction Miyabe, Haruka Uno, Atsuhiko Nakajima, Takahiro Morizane, Natsue Enomoto, Keisuke Hirose, Masayuki Hazama, Toshinori Takenaka, Yukinori Case Rep Otolaryngol Case Report Skull base osteomyelitis is classically documented as an extension of malignant otitis externa. Initial presentation commonly includes aural symptoms and cranial nerve dysfunctions. Here we present a case that emerged with multiple infarctions in the right cerebrum. A male in his 70s with diabetes mellitus and chronic renal failure presented with left hemiparesis. Imaging studies showed that blood flow in the carotid artery remained at the day of onset but was totally occluded 7 days later. However, collateral blood supply prevented severe infarction. These findings suggest that artery-to-artery embolization from the petrous and/or cavernous portion of the carotid artery caused the multiple infarctions observed on initial presentation. Osteomyelitis of the central skull base was diagnosed on the basis of the following findings taken together: laboratory results showing high levels of inflammation, presence of Pseudomonas aeruginosa in the otorrhea and blood culture, multiple cranial nerve palsies that appeared later, the bony erosion observed on CT, and the mass lesion on MRI. Osteomyelitis was treated successfully by long-term antibiotic therapy; however, the patient experienced cefepime-induced neurotoxicity during therapy. The potential involvement of the internal carotid artery in this rare and life-threatening disease is of particular interest in this case. Hindawi Publishing Corporation 2016 2016-08-11 /pmc/articles/PMC4997026/ /pubmed/27597916 http://dx.doi.org/10.1155/2016/9252361 Text en Copyright © 2016 Haruka Miyabe et al. https://creativecommons.org/licenses/by/4.0/ 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
Miyabe, Haruka
Uno, Atsuhiko
Nakajima, Takahiro
Morizane, Natsue
Enomoto, Keisuke
Hirose, Masayuki
Hazama, Toshinori
Takenaka, Yukinori
A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction
title A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction
title_full A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction
title_fullStr A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction
title_full_unstemmed A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction
title_short A Case of Skull Base Osteomyelitis with Multiple Cerebral Infarction
title_sort case of skull base osteomyelitis with multiple cerebral infarction
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997026/
https://www.ncbi.nlm.nih.gov/pubmed/27597916
http://dx.doi.org/10.1155/2016/9252361
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