[Prenatal diagnosis and postnatal outcome of isolated intra-abdominal calcifications: A 10-year experience from a referral fetal medicine center].

Diagnostic prénatal et issue néonatale des calcifications intra-abdominales isolées : étude rétrospective sur 10 ans.
Calcification intra-abdominale Calcification peritonéale Fetal hepatic hyperchogenicities Hyperéchogénicité hépatique fœtale Hyperéchogénicité péritonéale Intra-abdominal calcification Intra-peritoneal calcification Intraperitoneal echogenic foci

Journal

Gynecologie, obstetrique, fertilite & senologie
ISSN: 2468-7189
Titre abrégé: Gynecol Obstet Fertil Senol
Pays: France
ID NLM: 101693805

Informations de publication

Date de publication:
09 2019
Historique:
received: 28 03 2019
pubmed: 10 8 2019
medline: 12 3 2020
entrez: 10 8 2019
Statut: ppublish

Résumé

Intra-abdominal calcifications (iAC) detected during fetal ultrasound examinations are characterized by their isolated or associated nature, as well as their location. Our objective was to describe all cases of isolated iAC along with their etiological investigations and neonatal outcome, during a 10-year practice in a referral center. We conducted a retrospective descriptive monocentric study on neonates diagnosed with isolated iAC after antenatal expert ultrasound scan and referred to the Multidisciplinary Center for Prenatal Diagnosis at Trousseau Hospital and born between January 1st, 2008 and June 30th, 2018. The exclusion criteria were: retroperitoneal calcifications, iAC associated with other digestive abnormalities or with congenital malformations. The 32 isolated iAC cases accounted for 46% of all iAC. Nine cases were excluded for missing neonatal data. Among the 23 remaining isolated iAC cases, we observed 15 intra-hepatic calcifications, 5 peri-hepatic and two peritoneal calcifications. One fetus had both intra- and peri-hepatic calcifications. The majority of iAC remained stable throughout pregnancy. No cases of aneuploidy, fetal infection, or cystic fibrosis were detected. The neonatal outcome was favorable in all cases. In case of isolated and stable iAC after expert ultrasound scan, after having ruled out infectious diseases of the fetus and looked for the most frequent mutations of cystic fibrosis in the parents, the prognosis is favorable. Fetal karyotyping is recommended when additional structural anomalies are present.

Identifiants

pubmed: 31398445
pii: S2468-7189(19)30241-7
doi: 10.1016/j.gofs.2019.07.018
pii:
doi:

Types de publication

Journal Article

Langues

fre

Sous-ensembles de citation

IM

Pagination

643-649

Informations de copyright

Copyright © 2019 Elsevier Masson SAS. All rights reserved.

Auteurs

E Maisonneuve (E)

Service de médecine fœtale, centre pluridisciplinaire de diagnostic prénatal de l'Est Parisien, DMU ORIGYNE, médecine Sorbonne Université, hôpital Armand-Trousseau, AP-HP, 26, avenue du Dr Arnold-Netter, 75012 Paris, France. Electronic address: emelinem@yahoo.com.

L Debain (L)

Service de gynécologie-obstétrique, hôpital Trousseau, 75012 Paris, France.

C Garel (C)

Service de radiologie pédiatrique, hôpital Trousseau, 75012 Paris, France.

E Hervieux (E)

Service de chirurgie pédiatrique, hôpital Trousseau, 75012 Paris, France.

B Lafon (B)

Service de médecine fœtale, centre pluridisciplinaire de diagnostic prénatal de l'Est Parisien, DMU ORIGYNE, médecine Sorbonne Université, hôpital Armand-Trousseau, AP-HP, 26, avenue du Dr Arnold-Netter, 75012 Paris, France.

F Dhombres (F)

Service de médecine fœtale, centre pluridisciplinaire de diagnostic prénatal de l'Est Parisien, DMU ORIGYNE, médecine Sorbonne Université, hôpital Armand-Trousseau, AP-HP, 26, avenue du Dr Arnold-Netter, 75012 Paris, France; Médecine Sorbonne Université, 75013 Paris, France.

G Kayem (G)

Service de gynécologie-obstétrique, hôpital Trousseau, 75012 Paris, France; Médecine Sorbonne Université, 75013 Paris, France.

J-M Jouannic (JM)

Service de médecine fœtale, centre pluridisciplinaire de diagnostic prénatal de l'Est Parisien, DMU ORIGYNE, médecine Sorbonne Université, hôpital Armand-Trousseau, AP-HP, 26, avenue du Dr Arnold-Netter, 75012 Paris, France; Médecine Sorbonne Université, 75013 Paris, France.

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