LymphedemaV1, PubMed, Corpus, bibRecord, 005C09

[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].

Identifieur interne : 005C09 ( PubMed/Corpus ); précédent : 005C08; suivant : 005C10

[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].

Auteurs : S. Douvier ; J P Feldman ; A. Nivelon-Chevalier ; M. Degrolard ; M H Harran ; J. Jahier

Source :

Journal de gynecologie, obstetrique et biologie de la reproduction [ 0368-2315 ] ; 1991.

RBID : pubmed:2071861

English descriptors

KwdEn :
- Adult, Female, Fetal Diseases (diagnostic imaging), Fetal Diseases (genetics), Fetal Diseases (pathology), Humans, Karyotyping, Lymphangioma (diagnostic imaging), Lymphangioma (genetics), Lymphangioma (pathology), Lymphatic Diseases (diagnostic imaging), Lymphatic Diseases (genetics), Lymphatic Diseases (pathology), Phenotype, Pregnancy, Prognosis, Retrospective Studies, Ultrasonography, Prenatal.
MESH :
- diagnostic imaging : Fetal Diseases, Lymphangioma, Lymphatic Diseases.
- genetics : Fetal Diseases, Lymphangioma, Lymphatic Diseases.
- pathology : Fetal Diseases, Lymphangioma, Lymphatic Diseases.
- Adult, Female, Humans, Karyotyping, Phenotype, Pregnancy, Prognosis, Retrospective Studies, Ultrasonography, Prenatal.

Abstract

Fetal cystic hygroma (CH) are congenital malformation of the lymphatic system which are seen in antenatally ultrasonography from the end of the first trimester of pregnancy. From a 13 CH retrospective study, the authors discuss the ultrasound diagnosis, the prognosis and the management of CH. In our study, CH is associated with lymphedema (69%), hydrops (46%), diminution of amniotic fluid (69%) and other abnormality (31%). In all cases a diminution or an absence of fetal movement are found. In seven cases a cytogenetic analysis are performed on amniocentesis or fetal tissues: there are five 45XO, one 47XX + 13 and one 46XX. In six cases the chromosome culture failed: two male phenotypes and two histologic appearances of chromosomic anomaly. The prognosis depends on chromosome analysis, other ultrasound abnormality and the size of CH. It is usually fatal in utero. If chromosome anomaly are found, a genetic counsel is proposed.

PubMed: 2071861

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pubmed:2071861

Le document en format XML

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<author><name sortKey="Feldman, J P" sort="Feldman, J P" uniqKey="Feldman J" first="J P" last="Feldman">J P Feldman</name>
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<author><name sortKey="Nivelon Chevalier, A" sort="Nivelon Chevalier, A" uniqKey="Nivelon Chevalier A" first="A" last="Nivelon-Chevalier">A. Nivelon-Chevalier</name>
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<author><name sortKey="Degrolard, M" sort="Degrolard, M" uniqKey="Degrolard M" first="M" last="Degrolard">M. Degrolard</name>
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<author><name sortKey="Harran, M H" sort="Harran, M H" uniqKey="Harran M" first="M H" last="Harran">M H Harran</name>
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<front><div type="abstract" xml:lang="en">Fetal cystic hygroma (CH) are congenital malformation of the lymphatic system which are seen in antenatally ultrasonography from the end of the first trimester of pregnancy. From a 13 CH retrospective study, the authors discuss the ultrasound diagnosis, the prognosis and the management of CH. In our study, CH is associated with lymphedema (69%), hydrops (46%), diminution of amniotic fluid (69%) and other abnormality (31%). In all cases a diminution or an absence of fetal movement are found. In seven cases a cytogenetic analysis are performed on amniocentesis or fetal tissues: there are five 45XO, one 47XX + 13 and one 46XX. In six cases the chromosome culture failed: two male phenotypes and two histologic appearances of chromosomic anomaly. The prognosis depends on chromosome analysis, other ultrasound abnormality and the size of CH. It is usually fatal in utero. If chromosome anomaly are found, a genetic counsel is proposed.</div>
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<Abstract><AbstractText>Fetal cystic hygroma (CH) are congenital malformation of the lymphatic system which are seen in antenatally ultrasonography from the end of the first trimester of pregnancy. From a 13 CH retrospective study, the authors discuss the ultrasound diagnosis, the prognosis and the management of CH. In our study, CH is associated with lymphedema (69%), hydrops (46%), diminution of amniotic fluid (69%) and other abnormality (31%). In all cases a diminution or an absence of fetal movement are found. In seven cases a cytogenetic analysis are performed on amniocentesis or fetal tissues: there are five 45XO, one 47XX + 13 and one 46XX. In six cases the chromosome culture failed: two male phenotypes and two histologic appearances of chromosomic anomaly. The prognosis depends on chromosome analysis, other ultrasound abnormality and the size of CH. It is usually fatal in utero. If chromosome anomaly are found, a genetic counsel is proposed.</AbstractText>
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[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].

[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki