Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele
Background and Importance: This interesting case is about the presence of normal pressure hydrocephalus and a large pseudomeningocele at the same time after 13 months of posterior fossa surgery. Although the occurrence of a pseudomeningocele following posterior fossa surgery is not so rare, such a l...
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Format: | Article |
Language: | English |
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Guilan University of Medical Sciences
2017-09-01
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Series: | Iranian Journal of Neurosurgery |
Subjects: | |
Online Access: | http://irjns.org/browse.php?a_code=A-10-44-4&slc_lang=en&sid=1 |
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author | Ehsan Alimohammadi Guive Sharifi Mohammad Samadian Kaveh Ebrahimzadeh Omidvar Rezaei |
author_facet | Ehsan Alimohammadi Guive Sharifi Mohammad Samadian Kaveh Ebrahimzadeh Omidvar Rezaei |
author_sort | Ehsan Alimohammadi |
collection | DOAJ |
description | Background and Importance: This interesting case is about the presence of normal pressure hydrocephalus and a large pseudomeningocele at the same time after 13 months of posterior fossa surgery. Although the occurrence of a pseudomeningocele following posterior fossa surgery is not so rare, such a late large pseudomeningocele development with signs and symptoms of NPH after 13 months of surgery is rather peculiar.
Case Presentation: A 59-year-old man referred to our clinic for a cerebellopontine angle tumor. The patient presented with right hearing loss and mild facial palsy. We operated the patient with retrosigmoid approach, and we discharged him after five days. After about 13 months, the patient referred to our center again with complaint of progressive bulging of previous surgical region and gait apraxia, urinary incontinence and dementia. A large pseudomeningocele in the site of previous surgery was seen.
Conclusion: The authors presented a case report on late development (13 months) of a huge pseudomeningocele following vestibular schwannoma surgery with signs and symptoms of normal pressure hydrocephalus. Such a late big pseudomeningocele presentation with signs and symptoms of normal pressure hydrocephalus after posterior fossa surgery is peculiar. |
first_indexed | 2024-12-14T21:56:14Z |
format | Article |
id | doaj.art-de02d06ab6d94c1aba0210dc89029e2a |
institution | Directory Open Access Journal |
issn | 2423-6497 2423-6829 |
language | English |
last_indexed | 2024-12-14T21:56:14Z |
publishDate | 2017-09-01 |
publisher | Guilan University of Medical Sciences |
record_format | Article |
series | Iranian Journal of Neurosurgery |
spelling | doaj.art-de02d06ab6d94c1aba0210dc89029e2a2022-12-21T22:46:07ZengGuilan University of Medical SciencesIranian Journal of Neurosurgery2423-64972423-68292017-09-01327377Normal Pressure Hydrocephalus Presentation with a Large PseudomeningoceleEhsan Alimohammadi0Guive Sharifi1Mohammad Samadian2Kaveh Ebrahimzadeh3Omidvar Rezaei4 MD, Resident of Neurosurgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran MD, Associate Professor of Neurosurgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran MD, Associate Professor of Neurosurgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran MD, Assistant Professor of Neurosurgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran MD, Professor of Neurosurgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran Background and Importance: This interesting case is about the presence of normal pressure hydrocephalus and a large pseudomeningocele at the same time after 13 months of posterior fossa surgery. Although the occurrence of a pseudomeningocele following posterior fossa surgery is not so rare, such a late large pseudomeningocele development with signs and symptoms of NPH after 13 months of surgery is rather peculiar. Case Presentation: A 59-year-old man referred to our clinic for a cerebellopontine angle tumor. The patient presented with right hearing loss and mild facial palsy. We operated the patient with retrosigmoid approach, and we discharged him after five days. After about 13 months, the patient referred to our center again with complaint of progressive bulging of previous surgical region and gait apraxia, urinary incontinence and dementia. A large pseudomeningocele in the site of previous surgery was seen. Conclusion: The authors presented a case report on late development (13 months) of a huge pseudomeningocele following vestibular schwannoma surgery with signs and symptoms of normal pressure hydrocephalus. Such a late big pseudomeningocele presentation with signs and symptoms of normal pressure hydrocephalus after posterior fossa surgery is peculiar.http://irjns.org/browse.php?a_code=A-10-44-4&slc_lang=en&sid=1HydrocephalusPseudomeningoceleIntracranialPressure |
spellingShingle | Ehsan Alimohammadi Guive Sharifi Mohammad Samadian Kaveh Ebrahimzadeh Omidvar Rezaei Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele Iranian Journal of Neurosurgery Hydrocephalus Pseudomeningocele Intracranial Pressure |
title | Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele |
title_full | Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele |
title_fullStr | Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele |
title_full_unstemmed | Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele |
title_short | Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele |
title_sort | normal pressure hydrocephalus presentation with a large pseudomeningocele |
topic | Hydrocephalus Pseudomeningocele Intracranial Pressure |
url | http://irjns.org/browse.php?a_code=A-10-44-4&slc_lang=en&sid=1 |
work_keys_str_mv | AT ehsanalimohammadi normalpressurehydrocephaluspresentationwithalargepseudomeningocele AT guivesharifi normalpressurehydrocephaluspresentationwithalargepseudomeningocele AT mohammadsamadian normalpressurehydrocephaluspresentationwithalargepseudomeningocele AT kavehebrahimzadeh normalpressurehydrocephaluspresentationwithalargepseudomeningocele AT omidvarrezaei normalpressurehydrocephaluspresentationwithalargepseudomeningocele |