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Hydrocephalus in Encephalocele

dc.authorid Akyol, Mehmet Edip/0000-0002-5198-0219
dc.authorid Celegen, Izzet/0000-0002-2749-953X
dc.authorscopusid 57007941800
dc.authorscopusid 57837936900
dc.authorscopusid 57211033511
dc.authorscopusid 55439896900
dc.authorwosid Çeleğen, İzzet/Acx-8961-2022
dc.authorwosid Akyol, Mehmet/A-6865-2018
dc.contributor.author Akyol, M.E.
dc.contributor.author Çelegen, I.
dc.contributor.author Basar, I.
dc.contributor.author Arabaci, O.
dc.date.accessioned 2025-05-10T16:54:21Z
dc.date.available 2025-05-10T16:54:21Z
dc.date.issued 2022
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Akyol M.E., Department of Neurosurgery, Van YY University Faculty of Medicine, Van, Turkey; Çelegen I., Department of Public Health, Van YY University Faculty of Medicine, Van, Turkey; Basar I., Department of Neurosurgery, Dicle University, Faculty of Medicine, Diyarbakir, Turkey; Arabaci O., Department of Neurosurgery, Van YY University Faculty of Medicine, Van, Turkey en_US
dc.description.abstract OBJECTIVE: Encephalocele is a rare congenital neural tube defect (NTD) characterized by herniation of intracranial contents through a defect in the skull. In our study, encephalocele was diagnosed in our clinic and its association with hydrocephalus was evaluated. The effect of this association on the prognosis was discussed. PATIENTS AND METHODS: Patients who underwent surgery and follow-up with the diagnosis of encephalocele in the neurosurgery clinic of our hospital in an 8-year period from 2013 to 2021 were retrospectively examined. RESULTS: Patient records were obtained from the case notes of patients who underwent excision and repair for encephalocele. Of the 78 patients included in the study, 88.4% underwent surgery in the neonatal period. Moreover, 47% of the patients are male, and 31% are female. Encephalocele was present in 62.8% of patients and meningocele in 37.2%. Furthermore, 82.1% of encephalocele sacs were located in the occipital region. Chiari type 3 malformation was present in 57.6% of patients. Hydrocephalus developed in 56.4% of patients. There was an additional syndrome in 10.3% of the cases. The most common additional syndromes were corpus callosum dysgenesis with 39.7% and colpocephaly with 29.5%. The additional disease was present in 43.6% of patients. Preoperative and postoperative examination findings of more than half of patients were normal, but 33.3% were apathetic. Furthermore, 67.9% of patients, who underwent complete repair, survived, and 32.1% died. Hydrocephalus was present in 73.5% of patients with encephalocele (p<0.05). Hydrocephalus developed in 77.8% of patients with Chiari type 3 malformation (p<0.05). Hydrocephalus was found in 88.0% of patients with Ex (p<0.05). CONCLUSIONS: Encephalocele, which is a subgroup of NTD, differs clinically by its location and accompanying additional anomalies. In encephaloceles, the risk of morbidity and mortality can only be reduced with the multidisciplinary approach. Hydrocephalus and Chiari type 3 malformation are common in patients with encephalocele. These associations adversely affect the prognosis of the disease. Further research should be conducted on the evaluation of risk factors of NTD and methods of prevention from NTD. In this regard, we recommend that the training be repeated at certain intervals and that people’s awareness should be raised. © 2022 Verduci Editore s.r.l. All rights reserved. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.26355/eurrev_202208_29407
dc.identifier.endpage 5405 en_US
dc.identifier.issn 1128-3602
dc.identifier.issue 15 en_US
dc.identifier.pmid 35993634
dc.identifier.pmid 35993634
dc.identifier.scopus 2-s2.0-85135760365
dc.identifier.scopusquality Q2
dc.identifier.startpage 5399 en_US
dc.identifier.uri https://doi.org/10.26355/eurrev_202208_29407
dc.identifier.uri https://hdl.handle.net/20.500.14720/3100
dc.identifier.volume 26 en_US
dc.identifier.wos WOS:000864081200013
dc.identifier.wosquality Q2
dc.language.iso en en_US
dc.publisher Verduci Editore s.r.l en_US
dc.relation.ispartof European Review for Medical and Pharmacological Sciences en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Chiari Type 3 Malformation en_US
dc.subject Encephalocele en_US
dc.subject Hydrocephalus en_US
dc.subject Meningocele en_US
dc.subject Neural Tube Defect en_US
dc.title Hydrocephalus in Encephalocele en_US
dc.type Article en_US

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