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Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction

Ossification of pseudomeningocele is a rare occurrence and is one of the rare complications of ventriculoperitoneal (VP) shunt malfunction. We report a case of 12-year-old boy who came with features of raised intracranial pressure following shunt malfunction which was placed as a treatment to the aq...

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Autores principales: Bhatt, Anusha S., Mishra, Ajit M., Mhatre, Radhika, Nandeesh, Bevinahalli N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779559/
https://www.ncbi.nlm.nih.gov/pubmed/31595131
http://dx.doi.org/10.1055/s-0039-1695698
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author Bhatt, Anusha S.
Mishra, Ajit M.
Mhatre, Radhika
Nandeesh, Bevinahalli N.
author_facet Bhatt, Anusha S.
Mishra, Ajit M.
Mhatre, Radhika
Nandeesh, Bevinahalli N.
author_sort Bhatt, Anusha S.
collection PubMed
description Ossification of pseudomeningocele is a rare occurrence and is one of the rare complications of ventriculoperitoneal (VP) shunt malfunction. We report a case of 12-year-old boy who came with features of raised intracranial pressure following shunt malfunction which was placed as a treatment to the aqueductal stenosis. Computed tomography showed ventriculomegaly and hypodense collection in the occiput with posterior rim of calcification. The findings were confirmed on histopathology. Although ossified pseudomeningocele is a rare entity following VP shunt placement, it should be suspected if patients present with aggravated symptoms, especially if there is shunt malfunction as the treatment option varies with the presence or absence of resultant symptoms and ossification.
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spelling pubmed-67795592019-10-08 Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction Bhatt, Anusha S. Mishra, Ajit M. Mhatre, Radhika Nandeesh, Bevinahalli N. J Neurosci Rural Pract Ossification of pseudomeningocele is a rare occurrence and is one of the rare complications of ventriculoperitoneal (VP) shunt malfunction. We report a case of 12-year-old boy who came with features of raised intracranial pressure following shunt malfunction which was placed as a treatment to the aqueductal stenosis. Computed tomography showed ventriculomegaly and hypodense collection in the occiput with posterior rim of calcification. The findings were confirmed on histopathology. Although ossified pseudomeningocele is a rare entity following VP shunt placement, it should be suspected if patients present with aggravated symptoms, especially if there is shunt malfunction as the treatment option varies with the presence or absence of resultant symptoms and ossification. Thieme Medical and Scientific Publishers 2019-07 2019-10-07 /pmc/articles/PMC6779559/ /pubmed/31595131 http://dx.doi.org/10.1055/s-0039-1695698 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Bhatt, Anusha S.
Mishra, Ajit M.
Mhatre, Radhika
Nandeesh, Bevinahalli N.
Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction
title Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction
title_full Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction
title_fullStr Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction
title_full_unstemmed Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction
title_short Ossified Occipital Pseudomeningocele following Ventriculoperitoneal Shunt Malfunction
title_sort ossified occipital pseudomeningocele following ventriculoperitoneal shunt malfunction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779559/
https://www.ncbi.nlm.nih.gov/pubmed/31595131
http://dx.doi.org/10.1055/s-0039-1695698
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