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Meningocèle temporale et anophtalmie: à propos d´un cas

We here report the case of a 12-month old infant with congenital polymalformation including right temporal meningocele and homolateral eyeball aplasia. Brain CT scan confirmed this malformation with bone defect in the right temporal lobe, meningeal hernia containing cerebrospinal fluid and absence o...

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Autores principales: Rakotozanany, Patrick, Song, Miraulle Tien Yu, Ranoasy, Njara Francia, Rakotovao, Ketsia, Ratovondrainy, Willy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501746/
https://www.ncbi.nlm.nih.gov/pubmed/32983326
http://dx.doi.org/10.11604/pamj.2020.37.8.24930
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author Rakotozanany, Patrick
Song, Miraulle Tien Yu
Ranoasy, Njara Francia
Rakotovao, Ketsia
Ratovondrainy, Willy
author_facet Rakotozanany, Patrick
Song, Miraulle Tien Yu
Ranoasy, Njara Francia
Rakotovao, Ketsia
Ratovondrainy, Willy
author_sort Rakotozanany, Patrick
collection PubMed
description We here report the case of a 12-month old infant with congenital polymalformation including right temporal meningocele and homolateral eyeball aplasia. Brain CT scan confirmed this malformation with bone defect in the right temporal lobe, meningeal hernia containing cerebrospinal fluid and absence of the right eyeball. Surgery was performed to treat meningocele. Patient’s outcome was favorable. The purpose of this study was to highlight the rarity of this disease on the basis of a literature review.
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spelling pubmed-75017462020-09-24 Meningocèle temporale et anophtalmie: à propos d´un cas Rakotozanany, Patrick Song, Miraulle Tien Yu Ranoasy, Njara Francia Rakotovao, Ketsia Ratovondrainy, Willy Pan Afr Med J Case Report We here report the case of a 12-month old infant with congenital polymalformation including right temporal meningocele and homolateral eyeball aplasia. Brain CT scan confirmed this malformation with bone defect in the right temporal lobe, meningeal hernia containing cerebrospinal fluid and absence of the right eyeball. Surgery was performed to treat meningocele. Patient’s outcome was favorable. The purpose of this study was to highlight the rarity of this disease on the basis of a literature review. The African Field Epidemiology Network 2020-09-02 /pmc/articles/PMC7501746/ /pubmed/32983326 http://dx.doi.org/10.11604/pamj.2020.37.8.24930 Text en Copyright: Patrick Rakotozanany et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rakotozanany, Patrick
Song, Miraulle Tien Yu
Ranoasy, Njara Francia
Rakotovao, Ketsia
Ratovondrainy, Willy
Meningocèle temporale et anophtalmie: à propos d´un cas
title Meningocèle temporale et anophtalmie: à propos d´un cas
title_full Meningocèle temporale et anophtalmie: à propos d´un cas
title_fullStr Meningocèle temporale et anophtalmie: à propos d´un cas
title_full_unstemmed Meningocèle temporale et anophtalmie: à propos d´un cas
title_short Meningocèle temporale et anophtalmie: à propos d´un cas
title_sort meningocèle temporale et anophtalmie: à propos d´un cas
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501746/
https://www.ncbi.nlm.nih.gov/pubmed/32983326
http://dx.doi.org/10.11604/pamj.2020.37.8.24930
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