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Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report
BACKGROUND: Encephaloceles are rare phenomena which occur when brain parenchyma herniates through a skull defect which, if left untreated, may lead to significant issues such as cerebrospinal fluid (CSF) fistulas, meningitis, and intractable seizures. Due to the rarity and variety in size and locati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743700/ https://www.ncbi.nlm.nih.gov/pubmed/31528393 http://dx.doi.org/10.25259/SNI-137-2019 |
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author | Slavnic, Dejan Tong, Doris Barrett, Ryan Soo, Teck-Mun |
author_facet | Slavnic, Dejan Tong, Doris Barrett, Ryan Soo, Teck-Mun |
author_sort | Slavnic, Dejan |
collection | PubMed |
description | BACKGROUND: Encephaloceles are rare phenomena which occur when brain parenchyma herniates through a skull defect which, if left untreated, may lead to significant issues such as cerebrospinal fluid (CSF) fistulas, meningitis, and intractable seizures. Due to the rarity and variety in size and location of encephaloceles, no standard technique has been established for the resultant defect. Herein, we demonstrate the safe and effective use of bone morphogenetic protein (BMP) in the repair of CSF leak caused by encephalocele. CASE DESCRIPTION: A retrospective chart review was conducted on a 50-year-old female who presented with sudden onset spontaneous right nostril CSF leak due to the right lateral sphenoid sinus recess encephalocele, for which she underwent surgical repair. After resecting the encephalocele, cadaver crushed bone was used to fill the skull base defect. Following, an absorbable sponge from the extra-small BMP kit was cut in half and soaked with recombinant human BMP-2 (rhBMP-2) before being laid over the bony defect. On postoperative clinic visits at 2 weeks and at 3 months, the patient demonstrated good recovery without evidence of recurrent CSF leak. On follow-up computed tomography imaging at 9 months’ postsurgery, there was no evidence of recurrent CSF leak or encephalocele, infection, ectopic bone formation, excessive inflammation, or neoplasm. CONCLUSION: In this case, we demonstrate the successful use of BMP for the repair of CSF leak due to encephalocele. It is our extrapolation that the pro-inflammatory properties of rhBMP-2 lead to the prevention of recurrent CSF leak. |
format | Online Article Text |
id | pubmed-6743700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-67437002019-09-16 Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report Slavnic, Dejan Tong, Doris Barrett, Ryan Soo, Teck-Mun Surg Neurol Int Case Report BACKGROUND: Encephaloceles are rare phenomena which occur when brain parenchyma herniates through a skull defect which, if left untreated, may lead to significant issues such as cerebrospinal fluid (CSF) fistulas, meningitis, and intractable seizures. Due to the rarity and variety in size and location of encephaloceles, no standard technique has been established for the resultant defect. Herein, we demonstrate the safe and effective use of bone morphogenetic protein (BMP) in the repair of CSF leak caused by encephalocele. CASE DESCRIPTION: A retrospective chart review was conducted on a 50-year-old female who presented with sudden onset spontaneous right nostril CSF leak due to the right lateral sphenoid sinus recess encephalocele, for which she underwent surgical repair. After resecting the encephalocele, cadaver crushed bone was used to fill the skull base defect. Following, an absorbable sponge from the extra-small BMP kit was cut in half and soaked with recombinant human BMP-2 (rhBMP-2) before being laid over the bony defect. On postoperative clinic visits at 2 weeks and at 3 months, the patient demonstrated good recovery without evidence of recurrent CSF leak. On follow-up computed tomography imaging at 9 months’ postsurgery, there was no evidence of recurrent CSF leak or encephalocele, infection, ectopic bone formation, excessive inflammation, or neoplasm. CONCLUSION: In this case, we demonstrate the successful use of BMP for the repair of CSF leak due to encephalocele. It is our extrapolation that the pro-inflammatory properties of rhBMP-2 lead to the prevention of recurrent CSF leak. Scientific Scholar 2019-04-24 /pmc/articles/PMC6743700/ /pubmed/31528393 http://dx.doi.org/10.25259/SNI-137-2019 Text en Copyright: © 2019 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 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 | Case Report Slavnic, Dejan Tong, Doris Barrett, Ryan Soo, Teck-Mun Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report |
title | Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report |
title_full | Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report |
title_fullStr | Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report |
title_full_unstemmed | Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report |
title_short | Repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: A case report |
title_sort | repair of encephalocele and cerebrospinal fluid leak with the use of bone morphogenetic protein: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743700/ https://www.ncbi.nlm.nih.gov/pubmed/31528393 http://dx.doi.org/10.25259/SNI-137-2019 |
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