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Cerebral Abnormalities in Spina Bifida: A Neuropathological Study
INTRODUCTION: Spina bifida (SB) is the most common neural tube defect in humans. Here, we analyzed systematically the neuropathological findings of the brain in SB cases. METHODS: 79 cases with SB aperta (SBA) and 6 cases with SB occulta (SBO) autopsied at the Charité Neuropathology from 1974 to 200...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109215/ https://www.ncbi.nlm.nih.gov/pubmed/34614376 http://dx.doi.org/10.1177/10935266211040500 |
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author | Paschereit, Fabienne Schindelmann, Kim Hannah Hummel, Michael Schneider, Joanna Stoltenburg-Didinger, Gisela Kaindl, Angela M |
author_facet | Paschereit, Fabienne Schindelmann, Kim Hannah Hummel, Michael Schneider, Joanna Stoltenburg-Didinger, Gisela Kaindl, Angela M |
author_sort | Paschereit, Fabienne |
collection | PubMed |
description | INTRODUCTION: Spina bifida (SB) is the most common neural tube defect in humans. Here, we analyzed systematically the neuropathological findings of the brain in SB cases. METHODS: 79 cases with SB aperta (SBA) and 6 cases with SB occulta (SBO) autopsied at the Charité Neuropathology from 1974 to 2000 were re-evaluated retrospectively. For this, case files and spinal cord as well as brain sections were studied. RESULTS: While no brain malformations were detected in SBO cases, 95% of SBA cases had brain malformations. Main brain anomalies identified were hydrocephalus (71%), Chiari II malformation (36%), heterotopia (34%), other cerebellar anomalies (36%), gyrification defects (33%), and ependymal denudation (29%). Hydrocephalus was observed as early as gestational week 17 and was highly associated to Chiari II and ependymal denudation. In 55% SBA was accompanied by further anomalies not primarily affecting the CNS. CONCLUSION: We confirm using neuropathologic methods brain malformations in most SBA but none in SBO cases. In addition to our previous radiologic study, we now demonstrate the high prevalence of cerebellar malformations and cerebral heterotopias in SBA. The early detection of hydrocephalus and Chiari II malformation in fetuses raises the question whether these arise parallel rather than in strict temporal sequence. |
format | Online Article Text |
id | pubmed-9109215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-91092152022-05-17 Cerebral Abnormalities in Spina Bifida: A Neuropathological Study Paschereit, Fabienne Schindelmann, Kim Hannah Hummel, Michael Schneider, Joanna Stoltenburg-Didinger, Gisela Kaindl, Angela M Pediatr Dev Pathol Original Investigations INTRODUCTION: Spina bifida (SB) is the most common neural tube defect in humans. Here, we analyzed systematically the neuropathological findings of the brain in SB cases. METHODS: 79 cases with SB aperta (SBA) and 6 cases with SB occulta (SBO) autopsied at the Charité Neuropathology from 1974 to 2000 were re-evaluated retrospectively. For this, case files and spinal cord as well as brain sections were studied. RESULTS: While no brain malformations were detected in SBO cases, 95% of SBA cases had brain malformations. Main brain anomalies identified were hydrocephalus (71%), Chiari II malformation (36%), heterotopia (34%), other cerebellar anomalies (36%), gyrification defects (33%), and ependymal denudation (29%). Hydrocephalus was observed as early as gestational week 17 and was highly associated to Chiari II and ependymal denudation. In 55% SBA was accompanied by further anomalies not primarily affecting the CNS. CONCLUSION: We confirm using neuropathologic methods brain malformations in most SBA but none in SBO cases. In addition to our previous radiologic study, we now demonstrate the high prevalence of cerebellar malformations and cerebral heterotopias in SBA. The early detection of hydrocephalus and Chiari II malformation in fetuses raises the question whether these arise parallel rather than in strict temporal sequence. SAGE Publications 2021-10-06 2022-03 /pmc/articles/PMC9109215/ /pubmed/34614376 http://dx.doi.org/10.1177/10935266211040500 Text en © 2021, Society for Pediatric Pathology All rights reserved https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Investigations Paschereit, Fabienne Schindelmann, Kim Hannah Hummel, Michael Schneider, Joanna Stoltenburg-Didinger, Gisela Kaindl, Angela M Cerebral Abnormalities in Spina Bifida: A Neuropathological Study |
title | Cerebral Abnormalities in Spina Bifida: A Neuropathological Study |
title_full | Cerebral Abnormalities in Spina Bifida: A Neuropathological Study |
title_fullStr | Cerebral Abnormalities in Spina Bifida: A Neuropathological Study |
title_full_unstemmed | Cerebral Abnormalities in Spina Bifida: A Neuropathological Study |
title_short | Cerebral Abnormalities in Spina Bifida: A Neuropathological Study |
title_sort | cerebral abnormalities in spina bifida: a neuropathological study |
topic | Original Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109215/ https://www.ncbi.nlm.nih.gov/pubmed/34614376 http://dx.doi.org/10.1177/10935266211040500 |
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