The Myelic Limited Dorsal Malformation: Prenatal Ultrasonographic Characteristics of an Intermediate Form of Dysraphism.


Journal

Fetal diagnosis and therapy
ISSN: 1421-9964
Titre abrégé: Fetal Diagn Ther
Pays: Switzerland
ID NLM: 9107463

Informations de publication

Date de publication:
2021
Historique:
received: 07 05 2021
accepted: 16 08 2021
entrez: 23 11 2021
pubmed: 24 11 2021
medline: 26 11 2021
Statut: ppublish

Résumé

The aim of the study was to report a subtype of dysraphism designated as myelic limited dorsal malformation (MyeLDM) and to describe its characteristics at prenatal ultrasound (US). It was a retrospective study from 2014 to 2020 based on second-line US evaluation of patients referred to our institution for myelomeningocele (MMC). Magnetic resonance imaging and acetylcholine esterase evaluation in the amniotic fluid were also offered. Major and minor criteria for open and closed dysraphism were defined and recorded for each patient. Patients were included as MyeLDM when both criteria of closed and open dysraphism were observed in the same fetus. Correlations were obtained with the postpartum data. Twenty patients fulfilled the inclusion criteria, some of them being very close to MMC, others very close to limited dorsal myeloschisis (LDM), and others lying in between. There were 13 live-born neonates and 7 terminations of pregnancy. Correlations between prenatal and postpartum data were overall very good. Our series describe the ultrasonographic characteristics of an intermediate type of dysraphism and suggest that there is a continuum between MMC and LDM with numerous possibilities of hybrid forms (MyeLDM) sharing characteristics of both open and closed dysraphisms.

Identifiants

pubmed: 34814137
pii: 000519060
doi: 10.1159/000519060
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

690-700

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Saskia Vande Perre (S)

Service de Radiopédiatrie, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France, s.vandeperre@gmail.com.

Lucie Guilbaud (L)

Service de Médecine Fœtale, Centre de Référence Maladies Rares MAVEM, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Timothée de Saint-Denis (T)

Service de Neurochirurgie Pédiatrique, Centre de Référence Maladies Rares MAVEM, Hôpital Necker, AP-HP, Université de Paris, Paris, France.

Paul Maurice (P)

Service de Médecine Fœtale, Centre de Référence Maladies Rares MAVEM, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Pauline Lallemant-Dudek (P)

Service de Médecine Physique et Réadaptation Pédiatrique, AP-HP, Médecine Sorbonne Université, Paris, France.

Emeline Maisonneuve (E)

Service de Médecine Fœtale, Centre de Référence Maladies Rares MAVEM, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Ferdinand Dhombres (F)

Service de Médecine Fœtale, Centre de Référence Maladies Rares MAVEM, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Eléonore Blondiaux (E)

Service de Radiopédiatrie, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Hubert Ducou le Pointe (H)

Service de Radiopédiatrie, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Michel Zerah (M)

Service de Neurochirurgie Pédiatrique, Centre de Référence Maladies Rares MAVEM, Hôpital Necker, AP-HP, Université de Paris, Paris, France.

Jean-Marie Jouannic (JM)

Service de Médecine Fœtale, Centre de Référence Maladies Rares MAVEM, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

Catherine Garel (C)

Service de Radiopédiatrie, Hôpital Armand-Trousseau, AP-HP, Médecine Sorbonne Université, Paris, France.

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Classifications MeSH