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Giant mucopyocele associated with intracranial hypertension: Case report and literature review
BACKGROUND: Mucoceles are epithelial lined sacs that contain mucous. Eventually, they can be infected and so called mucopyoceles, which are usually slow growing lesions with common bone destruction located in the facial sinus. Mucoceles show multivariate etiology and occur between the fourth and sev...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655756/ https://www.ncbi.nlm.nih.gov/pubmed/29119040 http://dx.doi.org/10.4103/sni.sni_18_17 |
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author | Neves, Maick Willen Fernandes Pontelli, Luis Otavio Carneiro de Abreu Mattos, Luiz Gustavo Guimarães, Mariana Mazzuia Belsuzarri, Telmo Augusto Barba Gonçales, Tiago Fernandes Zeviani, Wolnei Marques de Aguiar, Paulo Henrique Pires Araújo, João Flavio Mattos |
author_facet | Neves, Maick Willen Fernandes Pontelli, Luis Otavio Carneiro de Abreu Mattos, Luiz Gustavo Guimarães, Mariana Mazzuia Belsuzarri, Telmo Augusto Barba Gonçales, Tiago Fernandes Zeviani, Wolnei Marques de Aguiar, Paulo Henrique Pires Araújo, João Flavio Mattos |
author_sort | Neves, Maick Willen Fernandes |
collection | PubMed |
description | BACKGROUND: Mucoceles are epithelial lined sacs that contain mucous. Eventually, they can be infected and so called mucopyoceles, which are usually slow growing lesions with common bone destruction located in the facial sinus. Mucoceles show multivariate etiology and occur between the fourth and seventh decade of life. CASE DESCRIPTION: Patient, 55-year-old, female, was referred unconscious with Cushing's triad to our department; she had fever since four days. The findings of skull computer tomography highlighted a large bifrontal lesion with an invasion of the rear wall of the frontal sinus, compression of the frontal lobes, and midline deviation. She was taken for an emergency surgery, which showed invasion of the dura and mucous infection. Postoperatively, there was a fast recovery of neurologic level and extubation on the second postoperative day. She took antibiotics for 14 days and was discharged from the hospital without neurologic deficits. CONCLUSIONS: Mucopyoceles are usually slow growing lesions that rarely increases rapidly. Our patient presented signs of intracranial hypertension; therefore, it was necessary to have quick surgical intervention. |
format | Online Article Text |
id | pubmed-5655756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56557562017-11-08 Giant mucopyocele associated with intracranial hypertension: Case report and literature review Neves, Maick Willen Fernandes Pontelli, Luis Otavio Carneiro de Abreu Mattos, Luiz Gustavo Guimarães, Mariana Mazzuia Belsuzarri, Telmo Augusto Barba Gonçales, Tiago Fernandes Zeviani, Wolnei Marques de Aguiar, Paulo Henrique Pires Araújo, João Flavio Mattos Surg Neurol Int General Neurosurgery: Case Report BACKGROUND: Mucoceles are epithelial lined sacs that contain mucous. Eventually, they can be infected and so called mucopyoceles, which are usually slow growing lesions with common bone destruction located in the facial sinus. Mucoceles show multivariate etiology and occur between the fourth and seventh decade of life. CASE DESCRIPTION: Patient, 55-year-old, female, was referred unconscious with Cushing's triad to our department; she had fever since four days. The findings of skull computer tomography highlighted a large bifrontal lesion with an invasion of the rear wall of the frontal sinus, compression of the frontal lobes, and midline deviation. She was taken for an emergency surgery, which showed invasion of the dura and mucous infection. Postoperatively, there was a fast recovery of neurologic level and extubation on the second postoperative day. She took antibiotics for 14 days and was discharged from the hospital without neurologic deficits. CONCLUSIONS: Mucopyoceles are usually slow growing lesions that rarely increases rapidly. Our patient presented signs of intracranial hypertension; therefore, it was necessary to have quick surgical intervention. Medknow Publications & Media Pvt Ltd 2017-10-10 /pmc/articles/PMC5655756/ /pubmed/29119040 http://dx.doi.org/10.4103/sni.sni_18_17 Text en Copyright: © 2017 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | General Neurosurgery: Case Report Neves, Maick Willen Fernandes Pontelli, Luis Otavio Carneiro de Abreu Mattos, Luiz Gustavo Guimarães, Mariana Mazzuia Belsuzarri, Telmo Augusto Barba Gonçales, Tiago Fernandes Zeviani, Wolnei Marques de Aguiar, Paulo Henrique Pires Araújo, João Flavio Mattos Giant mucopyocele associated with intracranial hypertension: Case report and literature review |
title | Giant mucopyocele associated with intracranial hypertension: Case report and literature review |
title_full | Giant mucopyocele associated with intracranial hypertension: Case report and literature review |
title_fullStr | Giant mucopyocele associated with intracranial hypertension: Case report and literature review |
title_full_unstemmed | Giant mucopyocele associated with intracranial hypertension: Case report and literature review |
title_short | Giant mucopyocele associated with intracranial hypertension: Case report and literature review |
title_sort | giant mucopyocele associated with intracranial hypertension: case report and literature review |
topic | General Neurosurgery: Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655756/ https://www.ncbi.nlm.nih.gov/pubmed/29119040 http://dx.doi.org/10.4103/sni.sni_18_17 |
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