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Le syndrome miroir: revue de la littérature illustrée par un cas

Mirror syndrome or Ballantyne syndrome is a rare disease, characterized by the association between fetal anasarca and maternal generalized edema. This may be complicated by pre-eclampsia. The purpose of this study was to highlight the diagnostic and therapeutic features of this severe clinical entit...

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Autores principales: Benchekroune, Khadija, Drissi, Jihad, Moukit, Mounir, Kouach, Jaouad, Moussaoui, Driss
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/PMC7755374/
https://www.ncbi.nlm.nih.gov/pubmed/33425158
http://dx.doi.org/10.11604/pamj.2020.37.125.19337
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author Benchekroune, Khadija
Drissi, Jihad
Moukit, Mounir
Kouach, Jaouad
Moussaoui, Driss
author_facet Benchekroune, Khadija
Drissi, Jihad
Moukit, Mounir
Kouach, Jaouad
Moussaoui, Driss
author_sort Benchekroune, Khadija
collection PubMed
description Mirror syndrome or Ballantyne syndrome is a rare disease, characterized by the association between fetal anasarca and maternal generalized edema. This may be complicated by pre-eclampsia. The purpose of this study was to highlight the diagnostic and therapeutic features of this severe clinical entity, which, despite its rarity, should be suspected. We here report the clinical case of a 35-year-old parturient woman at 26 weeks of amenorrhea presenting to the Emergency Department with idiopathic mirror syndrome whose progression was rapidly marked by the occurrence of intrauterine fetal death and remission of maternal clinical-biological symptoms, once uterine vacuity was obtained. Indeed, a specific treatment in uterus is necessary, although in some severe idiopathic cases, only uterine vacuity can improve maternal and fetal prognosis.
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spelling pubmed-77553742021-01-07 Le syndrome miroir: revue de la littérature illustrée par un cas Benchekroune, Khadija Drissi, Jihad Moukit, Mounir Kouach, Jaouad Moussaoui, Driss Pan Afr Med J Case Report Mirror syndrome or Ballantyne syndrome is a rare disease, characterized by the association between fetal anasarca and maternal generalized edema. This may be complicated by pre-eclampsia. The purpose of this study was to highlight the diagnostic and therapeutic features of this severe clinical entity, which, despite its rarity, should be suspected. We here report the clinical case of a 35-year-old parturient woman at 26 weeks of amenorrhea presenting to the Emergency Department with idiopathic mirror syndrome whose progression was rapidly marked by the occurrence of intrauterine fetal death and remission of maternal clinical-biological symptoms, once uterine vacuity was obtained. Indeed, a specific treatment in uterus is necessary, although in some severe idiopathic cases, only uterine vacuity can improve maternal and fetal prognosis. The African Field Epidemiology Network 2020-10-05 /pmc/articles/PMC7755374/ /pubmed/33425158 http://dx.doi.org/10.11604/pamj.2020.37.125.19337 Text en Copyright: Khadija Benchekroune 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
Benchekroune, Khadija
Drissi, Jihad
Moukit, Mounir
Kouach, Jaouad
Moussaoui, Driss
Le syndrome miroir: revue de la littérature illustrée par un cas
title Le syndrome miroir: revue de la littérature illustrée par un cas
title_full Le syndrome miroir: revue de la littérature illustrée par un cas
title_fullStr Le syndrome miroir: revue de la littérature illustrée par un cas
title_full_unstemmed Le syndrome miroir: revue de la littérature illustrée par un cas
title_short Le syndrome miroir: revue de la littérature illustrée par un cas
title_sort le syndrome miroir: revue de la littérature illustrée par un cas
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755374/
https://www.ncbi.nlm.nih.gov/pubmed/33425158
http://dx.doi.org/10.11604/pamj.2020.37.125.19337
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