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Terminal myelocystocele: Surgical management
BACKGROUND: The authors describe clinical and imaging findings, surgical technique, and outcomes in myelocystocele. METHODS: We describe a surgical procedure performed in six patients, four males and two females, with myelocystocele treated at our hospital. We review the images obtained at the time...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282762/ https://www.ncbi.nlm.nih.gov/pubmed/35855164 http://dx.doi.org/10.25259/SNI_299_2022 |
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author | Massa, Daniela Sol Montivero, Nicolas Arturo Medina, Santiago Adalberto Portillo |
author_facet | Massa, Daniela Sol Montivero, Nicolas Arturo Medina, Santiago Adalberto Portillo |
author_sort | Massa, Daniela Sol |
collection | PubMed |
description | BACKGROUND: The authors describe clinical and imaging findings, surgical technique, and outcomes in myelocystocele. METHODS: We describe a surgical procedure performed in six patients, four males and two females, with myelocystocele treated at our hospital. We review the images obtained at the time of diagnosis and after surgery. The patients’ age range was 12–56 months and had undergone surgery for terminal myelocystocele between 2015 and 2020. All patients had a large lumbar mass covered with healthy skin and presented spontaneous movements at birth. Two patients presented VACTERL syndrome. RESULTS: A watertight closure of the soft tissues was performed in all cases. None of the patients presented postsurgical complications, such as cerebrospinal fluid leak or infection. All the patients had undergone excision of the meningocele sacs, the tethering bands were lysed, and the filum was detethered. The mean follow-up period was 34 (12–56) months. A motor deficit was seen in 2 patients (33.3%). CONCLUSION: Prenatal diagnosis and early corrective surgical intervention are recommended to prevent deterioration in neurological function. VACTERL association is a common condition and should be investigated. |
format | Online Article Text |
id | pubmed-9282762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-92827622022-07-18 Terminal myelocystocele: Surgical management Massa, Daniela Sol Montivero, Nicolas Arturo Medina, Santiago Adalberto Portillo Surg Neurol Int Technical Notes BACKGROUND: The authors describe clinical and imaging findings, surgical technique, and outcomes in myelocystocele. METHODS: We describe a surgical procedure performed in six patients, four males and two females, with myelocystocele treated at our hospital. We review the images obtained at the time of diagnosis and after surgery. The patients’ age range was 12–56 months and had undergone surgery for terminal myelocystocele between 2015 and 2020. All patients had a large lumbar mass covered with healthy skin and presented spontaneous movements at birth. Two patients presented VACTERL syndrome. RESULTS: A watertight closure of the soft tissues was performed in all cases. None of the patients presented postsurgical complications, such as cerebrospinal fluid leak or infection. All the patients had undergone excision of the meningocele sacs, the tethering bands were lysed, and the filum was detethered. The mean follow-up period was 34 (12–56) months. A motor deficit was seen in 2 patients (33.3%). CONCLUSION: Prenatal diagnosis and early corrective surgical intervention are recommended to prevent deterioration in neurological function. VACTERL association is a common condition and should be investigated. Scientific Scholar 2022-06-03 /pmc/articles/PMC9282762/ /pubmed/35855164 http://dx.doi.org/10.25259/SNI_299_2022 Text en Copyright: © 2022 Surgical Neurology International https://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, transform, 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 | Technical Notes Massa, Daniela Sol Montivero, Nicolas Arturo Medina, Santiago Adalberto Portillo Terminal myelocystocele: Surgical management |
title | Terminal myelocystocele: Surgical management |
title_full | Terminal myelocystocele: Surgical management |
title_fullStr | Terminal myelocystocele: Surgical management |
title_full_unstemmed | Terminal myelocystocele: Surgical management |
title_short | Terminal myelocystocele: Surgical management |
title_sort | terminal myelocystocele: surgical management |
topic | Technical Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282762/ https://www.ncbi.nlm.nih.gov/pubmed/35855164 http://dx.doi.org/10.25259/SNI_299_2022 |
work_keys_str_mv | AT massadanielasol terminalmyelocystocelesurgicalmanagement AT montiveronicolasarturo terminalmyelocystocelesurgicalmanagement AT medinasantiagoadalbertoportillo terminalmyelocystocelesurgicalmanagement |